paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5 | DISCUSSION | 1 | 43 | [
"b35",
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] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Disruption of the RAD51 gene leads to cell death (43), whereas RAD51 paralogs including XRCC3 are not essential for cell viability. | [
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"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
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"55"
] | 131 | 6,800 | 1 | false | Disruption of the RAD51 gene leads to cell death, whereas RAD51 paralogs including XRCC3 are not essential for cell viability. | [
"43"
] | Disruption of the RAD51 gene leads to cell death, whereas RAD51 paralogs including XRCC3 are not essential for cell viability. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 44 | [
"b35",
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"b38",
"b44",
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"b47",
"b48",
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] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | The XRCC3-deficient X-ray sensitive hamster cell line, irs1SF shows increased chromosome mis-segregation (44) and has a 25-fold decrease in the frequency of error-free homology-directed repair of DNA DSBs (38). | [
"35",
"43",
"44",
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"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 210 | 6,801 | 1 | false | The XRCC3-deficient X-ray sensitive hamster cell line, irs1SF shows increased chromosome mis-segregation and has a 25-fold decrease in the frequency of error-free homology-directed repair of DNA DSBs. | [
"44",
"38"
] | The XRCC3-deficient X-ray sensitive hamster cell line, irs1SF shows increased chromosome mis-segregation and has a 25-fold decrease in the frequency of error-free homology-directed repair of DNA DSBs. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 44 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Both can be restored to wild-type levels through XRCC3 expression (44). | [
"35",
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"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
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"53",
"54",
"55"
] | 71 | 6,802 | 1 | false | Both can be restored to wild-type levels through XRCC3 expression. | [
"44"
] | Both can be restored to wild-type levels through XRCC3 expression. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | However, in contrast to RAD51, XRCC3 is known to act in the early as well as late stages of HR (45,46). | [
"35",
"43",
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"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 103 | 6,803 | 0 | false | However, in contrast to RAD51, XRCC3 is known to act in the early as well as late stages of HR. | [
"45,46"
] | However, in contrast to RAD51, XRCC3 is known to act in the early as well as late stages of HR. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Following reduction of XRCC3 mRNA levels we observed nearly complete elimination of rAAV-mediated gene targeting, which may reflect the multiple roles XRCC3 plays in HR. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 169 | 6,804 | 0 | false | Following reduction of XRCC3 mRNA levels we observed nearly complete elimination of rAAV-mediated gene targeting, which may reflect the multiple roles XRCC3 plays in HR. | [] | Following reduction of XRCC3 mRNA levels we observed nearly complete elimination of rAAV-mediated gene targeting, which may reflect the multiple roles XRCC3 plays in HR. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Although the reduction in XRCC3 mRNA was about 80% compared to mRNA levels in non-silenced cells, the remaining XRCC3 protein may be below a critical concentration. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 164 | 6,805 | 0 | false | Although the reduction in XRCC3 mRNA was about 80% compared to mRNA levels in non-silenced cells, the remaining XRCC3 protein may be below a critical concentration. | [] | Although the reduction in XRCC3 mRNA was about 80% compared to mRNA levels in non-silenced cells, the remaining XRCC3 protein may be below a critical concentration. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 47 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | A complex between XRCC3 and another RAD51 paralog, RAD51C associates specifically with single-stranded DNA (47) and modulates replication fork progression by slowing it down after DNA damage (48). | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 196 | 6,806 | 1 | false | A complex between XRCC3 and another RAD51 paralog, RAD51C associates specifically with single-stranded DNA and modulates replication fork progression by slowing it down after DNA damage. | [
"47",
"48"
] | A complex between XRCC3 and another RAD51 paralog, RAD51C associates specifically with single-stranded DNA and modulates replication fork progression by slowing it down after DNA damage. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | The complex also plays a role probably downstream of RAD54 in the HR pathway, i.e. | [
"35",
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"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 82 | 6,807 | 0 | false | The complex also plays a role probably downstream of RAD54 in the HR pathway, i.e. | [] | The complex also plays a role probably downstream of RAD54 in the HR pathway, i.e. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 49 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | as a resolvase of Holliday junctions (49). | [
"35",
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"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 42 | 6,808 | 1 | false | as a resolvase of Holliday junctions. | [
"49"
] | as a resolvase of Holliday junctions. | false | true | true | true | false | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Thus, resolution of recombination intermediates and/or triggering of DNA damage-related signaling present two of the possible roles for the XRCC3/RAD51C complex in rAAV targeting. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 179 | 6,809 | 0 | false | Thus, resolution of recombination intermediates and/or triggering of DNA damage-related signaling present two of the possible roles for the XRCC3/RAD51C complex in rAAV targeting. | [] | Thus, resolution of recombination intermediates and/or triggering of DNA damage-related signaling present two of the possible roles for the XRCC3/RAD51C complex in rAAV targeting. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 45 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | A recent report reveals that XRCC3 forms nuclear foci independently of RAD51 very early during homology-directed DSB repair, associates directly with DNA, and promotes formation of the RAD51 nucleoprotein filament (45). | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 219 | 6,810 | 1 | false | A recent report reveals that XRCC3 forms nuclear foci independently of RAD51 very early during homology-directed DSB repair, associates directly with DNA, and promotes formation of the RAD51 nucleoprotein filament. | [
"45"
] | A recent report reveals that XRCC3 forms nuclear foci independently of RAD51 very early during homology-directed DSB repair, associates directly with DNA, and promotes formation of the RAD51 nucleoprotein filament. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | One may hypothesize, that the absence of XRCC3 affects potential binding of RAD51 to the single-stranded AAV vector genome and subsequently its homologous pairing with the chromosomal locus during the targeting reaction. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 220 | 6,811 | 0 | false | One may hypothesize, that the absence of XRCC3 affects potential binding of RAD51 to the single-stranded AAV vector genome and subsequently its homologous pairing with the chromosomal locus during the targeting reaction. | [] | One may hypothesize, that the absence of XRCC3 affects potential binding of RAD51 to the single-stranded AAV vector genome and subsequently its homologous pairing with the chromosomal locus during the targeting reaction. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Based on this hypothesis we propose a molecular model for the mechanism of rAAV-mediated targeting in human cells (Figure 8). | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 125 | 6,812 | 0 | false | Based on this hypothesis we propose a molecular model for the mechanism of rAAV-mediated targeting in human cells (Figure 8). | [] | Based on this hypothesis we propose a molecular model for the mechanism of rAAV-mediated targeting in human cells (Figure 8). | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Removal of capsid proteins exposes the single-stranded AAV genome, allowing its degradation by nucleases. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 105 | 6,813 | 0 | false | Removal of capsid proteins exposes the single-stranded AAV genome, allowing its degradation by nucleases. | [] | Removal of capsid proteins exposes the single-stranded AAV genome, allowing its degradation by nucleases. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | There are several processes that could prevent this degradation: annealing of positive and negative viral genomes, second-strand synthesis, or coating of the single-stranded region by high-affinity single-stranded DNA-binding proteins, such as RPA. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 248 | 6,814 | 0 | false | There are several processes that could prevent this degradation: annealing of positive and negative viral genomes, second-strand synthesis, or coating of the single-stranded region by high-affinity single-stranded DNA-binding proteins, such as RPA. | [] | There are several processes that could prevent this degradation: annealing of positive and negative viral genomes, second-strand synthesis, or coating of the single-stranded region by high-affinity single-stranded DNA-binding proteins, such as RPA. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | RPA, a heterotrimer with multiple roles in DNA replication and repair, may ensure proper initiation of HR by preventing secondary structure formation from single-stranded DNA, thus supporting even coating by RAD51. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 214 | 6,815 | 0 | false | RPA, a heterotrimer with multiple roles in DNA replication and repair, may ensure proper initiation of HR by preventing secondary structure formation from single-stranded DNA, thus supporting even coating by RAD51. | [] | RPA, a heterotrimer with multiple roles in DNA replication and repair, may ensure proper initiation of HR by preventing secondary structure formation from single-stranded DNA, thus supporting even coating by RAD51. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | It is unknown, however, whether RPA affects the structure of the rAAV ITRs. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 75 | 6,816 | 0 | false | It is unknown, however, whether RPA affects the structure of the rAAV ITRs. | [] | It is unknown, however, whether RPA affects the structure of the rAAV ITRs. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 50 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | The RAD51C/XRCC3 heterodimer binds single-stranded AAV DNA at a terminal repeat site that resembles a DNA break (50), and through direct interactions between XRCC3 and RAD51 mediates the formation of the RAD51 nucleoprotein filament. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 233 | 6,817 | 1 | false | The RAD51C/XRCC3 heterodimer binds single-stranded AAV DNA at a terminal repeat site that resembles a DNA break, and through direct interactions between XRCC3 and RAD51 mediates the formation of the RAD51 nucleoprotein filament. | [
"50"
] | The RAD51C/XRCC3 heterodimer binds single-stranded AAV DNA at a terminal repeat site that resembles a DNA break, and through direct interactions between XRCC3 and RAD51 mediates the formation of the RAD51 nucleoprotein filament. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | RAD51 is likely derived from a mobile pool or from a BRCA2 complex, which also has a high binding affinity for ds- to single-stranded DNA transitions (51,52). | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 158 | 6,818 | 0 | false | RAD51 is likely derived from a mobile pool or from a BRCA2 complex, which also has a high binding affinity for ds- to single-stranded DNA transitions. | [
"51,52"
] | RAD51 is likely derived from a mobile pool or from a BRCA2 complex, which also has a high binding affinity for ds- to single-stranded DNA transitions. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 53 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | Following ATP binding and hydrolysis by XRCC3 the RAD51C/XRCC3 dimer may be destabilized (53). | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 94 | 6,819 | 1 | false | Following ATP binding and hydrolysis by XRCC3 the RAD51C/XRCC3 dimer may be destabilized. | [
"53"
] | Following ATP binding and hydrolysis by XRCC3 the RAD51C/XRCC3 dimer may be destabilized. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | and probably RAD54B interact with the RAD51 filament, unwind the ds genomic target DNA, and may remove nucleosomes from the homologous locus in order to prepare for pairing with the rAAV DNA. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 191 | 6,820 | 0 | false | and probably RAD54B interact with the RAD51 filament, unwind the ds genomic target DNA, and may remove nucleosomes from the homologous locus in order to prepare for pairing with the rAAV DNA. | [] | and probably RAD54B interact with the RAD51 filament, unwind the ds genomic target DNA, and may remove nucleosomes from the homologous locus in order to prepare for pairing with the rAAV DNA. | false | true | true | true | false | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | After pairing with the homologous target the resulting intermediate can be resolved either by crossing over and Holliday junction resolution or by the predominant pathway for DSB repair in mammalian cells—non-crossover gene conversion (54,55). | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 243 | 6,821 | 0 | false | After pairing with the homologous target the resulting intermediate can be resolved either by crossing over and Holliday junction resolution or by the predominant pathway for DSB repair in mammalian cells—non-crossover gene conversion. | [
"54,55"
] | After pairing with the homologous target the resulting intermediate can be resolved either by crossing over and Holliday junction resolution or by the predominant pathway for DSB repair in mammalian cells—non-crossover gene conversion. | true | true | true | true | true | 1,112 |
5 | DISCUSSION | 1 | 35 | [
"b35",
"b43",
"b44",
"b38",
"b44",
"b45",
"b46",
"b47",
"b48",
"b49",
"b45",
"b50",
"b51",
"b52",
"b53",
"b54",
"b55"
] | 16,822,856 | pmid-12456786|pmid-8943369|pmid-11025669|pmid-3347204|pmid-11025669|pmid-15372620|pmid-12191483|pmid-11751635|pmid-12718895|pmid-14716019|pmid-15372620|pmid-11459987|pmid-12228710|pmid-15703751|pmid-15037616|pmid-10880452|pmid-11356153 | The rAAV DNA serves as a template for repair of the chromosomal target, however, gene conversion can occur on the virus with the genomic sequence as a template. | [
"35",
"43",
"44",
"38",
"44",
"45",
"46",
"47",
"48",
"49",
"45",
"50",
"51",
"52",
"53",
"54",
"55"
] | 160 | 6,822 | 0 | false | The rAAV DNA serves as a template for repair of the chromosomal target, however, gene conversion can occur on the virus with the genomic sequence as a template. | [] | The rAAV DNA serves as a template for repair of the chromosomal target, however, gene conversion can occur on the virus with the genomic sequence as a template. | true | true | true | true | true | 1,112 |
6 | DISCUSSION | 1 | 56 | [
"b56"
] | 16,822,856 | pmid-8319297 | Our system shares significant similarity with a yeast model for gene targeting where donation of information to an unbroken chromosome is facilitated by a linearized plasmid (56). | [
"56"
] | 179 | 6,823 | 1 | false | Our system shares significant similarity with a yeast model for gene targeting where donation of information to an unbroken chromosome is facilitated by a linearized plasmid. | [
"56"
] | Our system shares significant similarity with a yeast model for gene targeting where donation of information to an unbroken chromosome is facilitated by a linearized plasmid. | true | true | true | true | true | 1,113 |
6 | DISCUSSION | 1 | 56 | [
"b56"
] | 16,822,856 | pmid-8319297 | The authors suggest this process occurs via the formation of a heteroduplex intermediate and the efficiency of donation depends on the spatial distribution of heteroduplex DNA. | [
"56"
] | 176 | 6,824 | 0 | false | The authors suggest this process occurs via the formation of a heteroduplex intermediate and the efficiency of donation depends on the spatial distribution of heteroduplex DNA. | [] | The authors suggest this process occurs via the formation of a heteroduplex intermediate and the efficiency of donation depends on the spatial distribution of heteroduplex DNA. | true | true | true | true | true | 1,113 |
6 | DISCUSSION | 1 | 56 | [
"b56"
] | 16,822,856 | pmid-8319297 | The frequency of donation was proportional to the increased distance from the break to the mutation and always resulted from a single gene conversion event, which is very likely to be the case with rAAV targeting. | [
"56"
] | 213 | 6,825 | 0 | false | The frequency of donation was proportional to the increased distance from the break to the mutation and always resulted from a single gene conversion event, which is very likely to be the case with rAAV targeting. | [] | The frequency of donation was proportional to the increased distance from the break to the mutation and always resulted from a single gene conversion event, which is very likely to be the case with rAAV targeting. | true | true | true | true | true | 1,113 |
7 | DISCUSSION | 1 | 30 | [
"b30",
"b57",
"b58",
"b59",
"b58"
] | 16,822,856 | pmid-15047832|pmid-15871683|pmid-12897142|pmid-9032269|pmid-12897142 | The conclusion that rAAV targeting depends on HR is in concert with recent evidence that targeting occurs with higher frequency in actively replicating cells, presumably the S phase of the cell cycle (30,57). | [
"30",
"57",
"58",
"59",
"58"
] | 208 | 6,826 | 0 | false | The conclusion that rAAV targeting depends on HR is in concert with recent evidence that targeting occurs with higher frequency in actively replicating cells, presumably the S phase of the cell cycle. | [
"30,57"
] | The conclusion that rAAV targeting depends on HR is in concert with recent evidence that targeting occurs with higher frequency in actively replicating cells, presumably the S phase of the cell cycle. | true | true | true | true | true | 1,114 |
7 | DISCUSSION | 1 | 58 | [
"b30",
"b57",
"b58",
"b59",
"b58"
] | 16,822,856 | pmid-15047832|pmid-15871683|pmid-12897142|pmid-9032269|pmid-12897142 | NHEJ and HR function in a complementary, overlapping manner (58) and the cell cycle phase determines the prevalence of one or the other repair process. | [
"30",
"57",
"58",
"59",
"58"
] | 151 | 6,827 | 1 | false | NHEJ and HR function in a complementary, overlapping manner and the cell cycle phase determines the prevalence of one or the other repair process. | [
"58"
] | NHEJ and HR function in a complementary, overlapping manner and the cell cycle phase determines the prevalence of one or the other repair process. | true | true | true | true | true | 1,114 |
7 | DISCUSSION | 1 | 58 | [
"b30",
"b57",
"b58",
"b59",
"b58"
] | 16,822,856 | pmid-15047832|pmid-15871683|pmid-12897142|pmid-9032269|pmid-12897142 | A predominant role for NHEJ early in the cell cycle in mammalian cells is supported for example by the high IR sensitivity of NHEJ-defective cells in the G1 phase (59), while HR seems to occur mostly during S and G2/M phases (58). | [
"30",
"57",
"58",
"59",
"58"
] | 230 | 6,828 | 1 | false | A predominant role for NHEJ early in the cell cycle in mammalian cells is supported for example by the high IR sensitivity of NHEJ-defective cells in the G1 phase, while HR seems to occur mostly during S and G2/M phases. | [
"59",
"58"
] | A predominant role for NHEJ early in the cell cycle in mammalian cells is supported for example by the high IR sensitivity of NHEJ-defective cells in the G1 phase, while HR seems to occur mostly during S and G2/M phases. | true | true | true | true | true | 1,114 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | A notable finding in our study is the significant decrease of GFP positive cells within 5 days after infection. | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 111 | 6,829 | 0 | false | A notable finding in our study is the significant decrease of GFP positive cells within 5 days after infection. | [] | A notable finding in our study is the significant decrease of GFP positive cells within 5 days after infection. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | This phenomenon has not yet been reported. | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 42 | 6,830 | 0 | false | This phenomenon has not yet been reported. | [] | This phenomenon has not yet been reported. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | Some of the rAAV targeting systems measured the number of events after an extended period of antibiotic selection (29). | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 119 | 6,831 | 1 | false | Some of the rAAV targeting systems measured the number of events after an extended period of antibiotic selection. | [
"29"
] | Some of the rAAV targeting systems measured the number of events after an extended period of antibiotic selection. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | Other systems are based on staining of the cells at a particular time point after infection (16,19). | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 100 | 6,832 | 0 | false | Other systems are based on staining of the cells at a particular time point after infection. | [
"16,19"
] | Other systems are based on staining of the cells at a particular time point after infection. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | In yet another system, which uses GFP as a readout in living cells, the results were given for only one time point, i.e. | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 120 | 6,833 | 0 | false | In yet another system, which uses GFP as a readout in living cells, the results were given for only one time point, i.e. | [] | In yet another system, which uses GFP as a readout in living cells, the results were given for only one time point, i.e. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 30 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | as positive foci at day 7 (30). | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 31 | 6,834 | 1 | false | as positive foci at day 7. | [
"30"
] | as positive foci at day 7. | false | true | true | true | false | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | The higher number of GFP positive cells at early time-points could also imply asymmetric recognition of the rAAV ITRs by a component of the cellular recombination machinery. | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 173 | 6,835 | 0 | false | The higher number of GFP positive cells at early time-points could also imply asymmetric recognition of the rAAV ITRs by a component of the cellular recombination machinery. | [] | The higher number of GFP positive cells at early time-points could also imply asymmetric recognition of the rAAV ITRs by a component of the cellular recombination machinery. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | That is, gene conversion on the viral vector instead of on the genomic target may have occurred. | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 96 | 6,836 | 0 | false | That is, gene conversion on the viral vector instead of on the genomic target may have occurred. | [] | That is, gene conversion on the viral vector instead of on the genomic target may have occurred. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | This may happen, for example, if a nick occurs at a hot-spot on the viral DNA within the double-stranded (60,61) or single-stranded region with subsequent invasion and copying of the chromosomal DNA sequence to repair the vector mutation. | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 238 | 6,837 | 0 | false | This may happen, for example, if a nick occurs at a hot-spot on the viral DNA within the double-stranded or single-stranded region with subsequent invasion and copying of the chromosomal DNA sequence to repair the vector mutation. | [
"60,61"
] | This may happen, for example, if a nick occurs at a hot-spot on the viral DNA within the double-stranded or single-stranded region with subsequent invasion and copying of the chromosomal DNA sequence to repair the vector mutation. | true | true | true | true | true | 1,115 |
8 | DISCUSSION | 1 | 29 | [
"b29",
"b16",
"b19",
"b30",
"b60",
"b61"
] | 16,822,856 | pmid-9537413|pmid-12724413|pmid-10775597|pmid-15047832|pmid-15208627|pmid-15731255 | The unusual structure of the ITRs and the ss–ds transitional regions may be likely targets for nucleases. | [
"29",
"16",
"19",
"30",
"60",
"61"
] | 105 | 6,838 | 0 | false | The unusual structure of the ITRs and the ss–ds transitional regions may be likely targets for nucleases. | [] | The unusual structure of the ITRs and the ss–ds transitional regions may be likely targets for nucleases. | true | true | true | true | true | 1,115 |
9 | DISCUSSION | 1 | 62 | [
"b62",
"b63",
"b64"
] | 16,822,856 | pmid-12941339|pmid-12140331|pmid-10455437 | Our results together with previous data provide the groundwork for improvement of the rAAV targeting frequency by shifting the balance from the NHEJ to the HR pathway. | [
"62",
"63",
"64"
] | 167 | 6,839 | 0 | false | Our results together with previous data provide the groundwork for improvement of the rAAV targeting frequency by shifting the balance from the NHEJ to the HR pathway. | [] | Our results together with previous data provide the groundwork for improvement of the rAAV targeting frequency by shifting the balance from the NHEJ to the HR pathway. | true | true | true | true | true | 1,116 |
9 | DISCUSSION | 1 | 62 | [
"b62",
"b63",
"b64"
] | 16,822,856 | pmid-12941339|pmid-12140331|pmid-10455437 | Since DNA-PK does not affect gene targeting, specific inhibition of DNA-PK with chemically synthesized small molecules (62), which has been shown to enhance gene conversion (63), combined with overexpression of proteins promoting HR (64) or synchronization of cells in S phase (for targeting of stem-cells) would enhance... | [
"62",
"63",
"64"
] | 406 | 6,840 | 1 | false | Since DNA-PK does not affect gene targeting, specific inhibition of DNA-PK with chemically synthesized small molecules, which has been shown to enhance gene conversion, combined with overexpression of proteins promoting HR or synchronization of cells in S phase (for targeting of stem-cells) would enhance further target... | [
"62",
"63",
"64"
] | Since DNA-PK does not affect gene targeting, specific inhibition of DNA-PK with chemically synthesized small molecules, which has been shown to enhance gene conversion, combined with overexpression of proteins promoting HR or synchronization of cells in S phase (for targeting of stem-cells) would enhance further target... | true | true | true | true | true | 1,116 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4 B5 B6 B7",
"B8",
"B9",
"B10",
"B11"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | The influenza A viruses are members of the family Orthomyxoviridae with a genome consisting of eight single-stranded RNA segments of negative polarity. | [
"1",
"2",
"3",
"4–7",
"8",
"9",
"10",
"11"
] | 151 | 6,841 | 0 | false | The influenza A viruses are members of the family Orthomyxoviridae with a genome consisting of eight single-stranded RNA segments of negative polarity. | [] | The influenza A viruses are members of the family Orthomyxoviridae with a genome consisting of eight single-stranded RNA segments of negative polarity. | true | true | true | true | true | 1,117 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4 B5 B6 B7",
"B8",
"B9",
"B10",
"B11"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Each one is encapsidated by binding to the polymerase complex and to a number of nucleoprotein (NP) monomers (1), forming a ribonucleoprotein (RNP) complex (2). | [
"1",
"2",
"3",
"4–7",
"8",
"9",
"10",
"11"
] | 160 | 6,842 | 1 | false | Each one is encapsidated by binding to the polymerase complex and to a number of nucleoprotein (NP) monomers, forming a ribonucleoprotein (RNP) complex. | [
"1",
"2"
] | Each one is encapsidated by binding to the polymerase complex and to a number of nucleoprotein (NP) monomers, forming a ribonucleoprotein (RNP) complex. | true | true | true | true | true | 1,117 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4 B5 B6 B7",
"B8",
"B9",
"B10",
"B11"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Transcription and replication of each virus RNP take place in the nucleus of the infected cell [reviewed in (3)] and hence viral mRNAs are potential substrates for the cellular splicing machinery and need to be exported from the nucleus to express the viral proteins. | [
"1",
"2",
"3",
"4–7",
"8",
"9",
"10",
"11"
] | 267 | 6,843 | 0 | false | Transcription and replication of each virus RNP take place in the nucleus of the infected cell and hence viral mRNAs are potential substrates for the cellular splicing machinery and need to be exported from the nucleus to express the viral proteins. | [
"reviewed in (3)"
] | Transcription and replication of each virus RNP take place in the nucleus of the infected cell and hence viral mRNAs are potential substrates for the cellular splicing machinery and need to be exported from the nucleus to express the viral proteins. | true | true | true | true | true | 1,117 |
0 | INTRODUCTION | 1 | 4–7 | [
"B1",
"B2",
"B3",
"B4 B5 B6 B7",
"B8",
"B9",
"B10",
"B11"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Indeed, the collinear transcripts from segments 7 and 8 can be directly expressed or can become spliced to generate M1 and M2 or NS1 and NEP(NS2) proteins, respectively (4–7). | [
"1",
"2",
"3",
"4–7",
"8",
"9",
"10",
"11"
] | 175 | 6,844 | 1 | false | Indeed, the collinear transcripts from segments 7 and 8 can be directly expressed or can become spliced to generate M1 and M2 or NS1 and NEP proteins, respectively. | [
"NS2",
"4–7"
] | Indeed, the collinear transcripts from segments 7 and 8 can be directly expressed or can become spliced to generate M1 and M2 or NS1 and NEP proteins, respectively. | true | true | true | true | true | 1,117 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4 B5 B6 B7",
"B8",
"B9",
"B10",
"B11"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | In productively infected cells, these splicing events are regulated in such a way that the steady-state ratios of spliced versus non-spliced mRNAs is only a few percent [reviewed in (8)]. | [
"1",
"2",
"3",
"4–7",
"8",
"9",
"10",
"11"
] | 187 | 6,845 | 0 | false | In productively infected cells, these splicing events are regulated in such a way that the steady-state ratios of spliced versus non-spliced mRNAs is only a few percent. | [
"reviewed in (8)"
] | In productively infected cells, these splicing events are regulated in such a way that the steady-state ratios of spliced versus non-spliced mRNAs is only a few percent. | true | true | true | true | true | 1,117 |
0 | INTRODUCTION | 1 | 9 | [
"B1",
"B2",
"B3",
"B4 B5 B6 B7",
"B8",
"B9",
"B10",
"B11"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | These relative levels can be modified in non-productive cells (9) or by virus mutation (10) and are not constant along virus infection (11), suggesting the involvement of virus and cellular factors in the regulation of virus mRNA splicing. | [
"1",
"2",
"3",
"4–7",
"8",
"9",
"10",
"11"
] | 239 | 6,846 | 1 | false | These relative levels can be modified in non-productive cells or by virus mutation and are not constant along virus infection, suggesting the involvement of virus and cellular factors in the regulation of virus mRNA splicing. | [
"9",
"10",
"11"
] | These relative levels can be modified in non-productive cells or by virus mutation and are not constant along virus infection, suggesting the involvement of virus and cellular factors in the regulation of virus mRNA splicing. | true | true | true | true | true | 1,117 |
1 | INTRODUCTION | 1 | 12–14 | [
"B12 B13 B14",
"B15",
"B16 B17 B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25",
"B26",
"B24",
"B27",
"B28",
"B29",
"B20",
"B30 B31 B32",
"B33",
"B34",
"B35"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | The NS1 protein is a crucial regulatory factor during virus infection [reviewed in (12–14)], affecting cellular and viral gene expression and virus counteraction of the interferon response. | [
"12–14",
"15",
"16–18",
"19",
"20",
"21",
"22",
"23",
"24",
"25",
"26",
"24",
"27",
"28",
"29",
"20",
"30–32",
"33",
"34",
"35"
] | 189 | 6,847 | 0 | false | The NS1 protein is a crucial regulatory factor during virus infection, affecting cellular and viral gene expression and virus counteraction of the interferon response. | [
"reviewed in (12–14)"
] | The NS1 protein is a crucial regulatory factor during virus infection, affecting cellular and viral gene expression and virus counteraction of the interferon response. | true | true | true | true | true | 1,118 |
1 | INTRODUCTION | 1 | 15 | [
"B12 B13 B14",
"B15",
"B16 B17 B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25",
"B26",
"B24",
"B27",
"B28",
"B29",
"B20",
"B30 B31 B32",
"B33",
"B34",
"B35"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | It accumulates in the nucleus early during virus infection (15) and when expressed from cloned DNA (16–18), but it can be found in association with polysomes later in the infection (19,20). | [
"12–14",
"15",
"16–18",
"19",
"20",
"21",
"22",
"23",
"24",
"25",
"26",
"24",
"27",
"28",
"29",
"20",
"30–32",
"33",
"34",
"35"
] | 189 | 6,848 | 1 | false | It accumulates in the nucleus early during virus infection and when expressed from cloned DNA, but it can be found in association with polysomes later in the infection. | [
"15",
"16–18",
"19,20"
] | It accumulates in the nucleus early during virus infection and when expressed from cloned DNA, but it can be found in association with polysomes later in the infection. | true | true | true | true | true | 1,118 |
1 | INTRODUCTION | 1 | 25 | [
"B12 B13 B14",
"B15",
"B16 B17 B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25",
"B26",
"B24",
"B27",
"B28",
"B29",
"B20",
"B30 B31 B32",
"B33",
"B34",
"B35"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | NS1 is a RNA-binding protein that interacts in vitro with dsRNA (21,22), vRNA (23,24), poly-A-containing RNAs (25) and U6 snRNA (26). | [
"12–14",
"15",
"16–18",
"19",
"20",
"21",
"22",
"23",
"24",
"25",
"26",
"24",
"27",
"28",
"29",
"20",
"30–32",
"33",
"34",
"35"
] | 133 | 6,849 | 1 | false | NS1 is a RNA-binding protein that interacts in vitro with dsRNA, vRNA, poly-A-containing RNAs and U6 snRNA. | [
"21,22",
"23,24",
"25",
"26"
] | NS1 is a RNA-binding protein that interacts in vitro with dsRNA, vRNA, poly-A-containing RNAs and U6 snRNA. | true | true | true | true | true | 1,118 |
1 | INTRODUCTION | 1 | 28 | [
"B12 B13 B14",
"B15",
"B16 B17 B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25",
"B26",
"B24",
"B27",
"B28",
"B29",
"B20",
"B30 B31 B32",
"B33",
"B34",
"B35"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | The RNA-binding domain is located within the N-terminal half of the protein (24,27), and the rest of the protein appears to contain an effector domain (28). | [
"12–14",
"15",
"16–18",
"19",
"20",
"21",
"22",
"23",
"24",
"25",
"26",
"24",
"27",
"28",
"29",
"20",
"30–32",
"33",
"34",
"35"
] | 156 | 6,850 | 1 | false | The RNA-binding domain is located within the N-terminal half of the protein, and the rest of the protein appears to contain an effector domain. | [
"24,27",
"28"
] | The RNA-binding domain is located within the N-terminal half of the protein, and the rest of the protein appears to contain an effector domain. | true | true | true | true | true | 1,118 |
1 | INTRODUCTION | 1 | 12–14 | [
"B12 B13 B14",
"B15",
"B16 B17 B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25",
"B26",
"B24",
"B27",
"B28",
"B29",
"B20",
"B30 B31 B32",
"B33",
"B34",
"B35"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | NS1 protein interacts with many viral and cellular factors. | [
"12–14",
"15",
"16–18",
"19",
"20",
"21",
"22",
"23",
"24",
"25",
"26",
"24",
"27",
"28",
"29",
"20",
"30–32",
"33",
"34",
"35"
] | 59 | 6,851 | 0 | false | NS1 protein interacts with many viral and cellular factors. | [] | NS1 protein interacts with many viral and cellular factors. | true | true | true | true | true | 1,118 |
1 | INTRODUCTION | 1 | 29 | [
"B12 B13 B14",
"B15",
"B16 B17 B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25",
"B26",
"B24",
"B27",
"B28",
"B29",
"B20",
"B30 B31 B32",
"B33",
"B34",
"B35"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | These include the virus RNP and/or polymerase (29), cellular proteins involved in translation, like hStaufen, PABPI and eIF4G (20,30–32) and cellular factors involved in post-transcriptional processing of RNA, like CPSF (33), PABPII (34) and NS1–BP, a potential splicing-related factor (35). | [
"12–14",
"15",
"16–18",
"19",
"20",
"21",
"22",
"23",
"24",
"25",
"26",
"24",
"27",
"28",
"29",
"20",
"30–32",
"33",
"34",
"35"
] | 291 | 6,852 | 1 | false | These include the virus RNP and/or polymerase, cellular proteins involved in translation, like hStaufen, PABPI and eIF4G and cellular factors involved in post-transcriptional processing of RNA, like CPSF, PABPII and NS1–BP, a potential splicing-related factor. | [
"29",
"20,30–32",
"33",
"34",
"35"
] | These include the virus RNP and/or polymerase, cellular proteins involved in translation, like hStaufen, PABPI and eIF4G and cellular factors involved in post-transcriptional processing of RNA, like CPSF, PABPII and NS1–BP, a potential splicing-related factor. | true | true | true | true | true | 1,118 |
2 | INTRODUCTION | 1 | 36 | [
"B36",
"B37",
"B38",
"B16",
"B39",
"B40",
"B41"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | The splicing of NS1 mRNA has been studied in vitro. | [
"36",
"37",
"38",
"16",
"39",
"40",
"41"
] | 51 | 6,853 | 0 | false | The splicing of NS1 mRNA has been studied in vitro. | [] | The splicing of NS1 mRNA has been studied in vitro. | true | true | true | true | true | 1,119 |
2 | INTRODUCTION | 1 | 36 | [
"B36",
"B37",
"B38",
"B16",
"B39",
"B40",
"B41"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | Early work indicated that it is a non-spliceable transcript under normal in vitro conditions (36), due the block after formation of a 55S pre-splicing complex (37). | [
"36",
"37",
"38",
"16",
"39",
"40",
"41"
] | 164 | 6,854 | 1 | false | Early work indicated that it is a non-spliceable transcript under normal in vitro conditions, due the block after formation of a 55S pre-splicing complex. | [
"36",
"37"
] | Early work indicated that it is a non-spliceable transcript under normal in vitro conditions, due the block after formation of a 55S pre-splicing complex. | true | true | true | true | true | 1,119 |
2 | INTRODUCTION | 1 | 38 | [
"B36",
"B37",
"B38",
"B16",
"B39",
"B40",
"B41"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | Subsequent mapping experiments led to the identification of RNA sequences within NS1 mRNA that may down-regulate its splicing efficiency (38). | [
"36",
"37",
"38",
"16",
"39",
"40",
"41"
] | 142 | 6,855 | 1 | false | Subsequent mapping experiments led to the identification of RNA sequences within NS1 mRNA that may down-regulate its splicing efficiency. | [
"38"
] | Subsequent mapping experiments led to the identification of RNA sequences within NS1 mRNA that may down-regulate its splicing efficiency. | true | true | true | true | true | 1,119 |
2 | INTRODUCTION | 1 | 36 | [
"B36",
"B37",
"B38",
"B16",
"B39",
"B40",
"B41"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | In vivo studies have also been carried out to analyze the splicing of NS1 mRNA. | [
"36",
"37",
"38",
"16",
"39",
"40",
"41"
] | 79 | 6,856 | 0 | false | In vivo studies have also been carried out to analyze the splicing of NS1 mRNA. | [] | In vivo studies have also been carried out to analyze the splicing of NS1 mRNA. | true | true | true | true | true | 1,119 |
2 | INTRODUCTION | 1 | 36 | [
"B36",
"B37",
"B38",
"B16",
"B39",
"B40",
"B41"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | When expressed from a RNA PolII-driven cDNA it can be spliced (16,39) and its splicing can be blocked in trans by the expression of the encoded NS1 protein (40,41). | [
"36",
"37",
"38",
"16",
"39",
"40",
"41"
] | 164 | 6,857 | 0 | false | When expressed from a RNA PolII-driven cDNA it can be spliced and its splicing can be blocked in trans by the expression of the encoded NS1 protein. | [
"16,39",
"40,41"
] | When expressed from a RNA PolII-driven cDNA it can be spliced and its splicing can be blocked in trans by the expression of the encoded NS1 protein. | true | true | true | true | true | 1,119 |
3 | INTRODUCTION | 1 | 25 | [
"B25",
"B28",
"B41",
"B33",
"B42"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-11421366|pmid-9696811|pmid-8313914|pmid-9049349|pmid-12667806 | In addition of the splicing inhibition, PolII-driven expression of NS1 from a cDNA led to a general retention of mRNAs in the nucleus (25,28,41). | [
"25",
"28",
"41",
"33",
"42"
] | 145 | 6,858 | 0 | false | In addition of the splicing inhibition, PolII-driven expression of NS1 from a cDNA led to a general retention of mRNAs in the nucleus. | [
"25,28,41"
] | In addition of the splicing inhibition, PolII-driven expression of NS1 from a cDNA led to a general retention of mRNAs in the nucleus. | true | true | true | true | true | 1,120 |
3 | INTRODUCTION | 1 | 33 | [
"B25",
"B28",
"B41",
"B33",
"B42"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-11421366|pmid-9696811|pmid-8313914|pmid-9049349|pmid-12667806 | The interaction of NS1 with the CPSF polyadenylation factor (33) suggested a mechanism for this transport block, as NS1–CPSF interaction would inhibit the 3′-processing of cellular transcripts. | [
"25",
"28",
"41",
"33",
"42"
] | 193 | 6,859 | 1 | false | The interaction of NS1 with the CPSF polyadenylation factor suggested a mechanism for this transport block, as NS1–CPSF interaction would inhibit the 3′-processing of cellular transcripts. | [
"33"
] | The interaction of NS1 with the CPSF polyadenylation factor suggested a mechanism for this transport block, as NS1–CPSF interaction would inhibit the 3′-processing of cellular transcripts. | true | true | true | true | true | 1,120 |
3 | INTRODUCTION | 1 | 42 | [
"B25",
"B28",
"B41",
"B33",
"B42"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-11421366|pmid-9696811|pmid-8313914|pmid-9049349|pmid-12667806 | Furthermore, it was proposed that CPSF interaction would indirectly down-regulate the splicing of cellular, but not viral, single-intron containing transcripts (42). | [
"25",
"28",
"41",
"33",
"42"
] | 165 | 6,860 | 1 | false | Furthermore, it was proposed that CPSF interaction would indirectly down-regulate the splicing of cellular, but not viral, single-intron containing transcripts. | [
"42"
] | Furthermore, it was proposed that CPSF interaction would indirectly down-regulate the splicing of cellular, but not viral, single-intron containing transcripts. | true | true | true | true | true | 1,120 |
4 | INTRODUCTION | 0 | null | null | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | The main limitation of these in vivo studies is that NS1 expression was carried out by transfection and the ‘viral’ mRNAs analysed are indeed PolII-driven transcripts. | null | 167 | 6,861 | 0 | false | null | null | The main limitation of these in vivo studies is that NS1 expression was carried out by transfection and the ‘viral’ mRNAs analysed are indeed PolII-driven transcripts. | true | true | true | true | true | 1,121 |
4 | INTRODUCTION | 0 | null | null | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | To avoid these problems we have established a transient virus replication-transcription system in vivo in which a recombinant NS RNP is amplified and transcribed by the viral polymerase. | null | 186 | 6,862 | 0 | false | null | null | To avoid these problems we have established a transient virus replication-transcription system in vivo in which a recombinant NS RNP is amplified and transcribed by the viral polymerase. | true | true | true | true | true | 1,121 |
4 | INTRODUCTION | 0 | null | null | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | Using this more physiological system we show here that NS1 protein down-regulates the splicing and block the nuclear export of its own viral mRNA. | null | 146 | 6,863 | 0 | false | null | null | Using this more physiological system we show here that NS1 protein down-regulates the splicing and block the nuclear export of its own viral mRNA. | true | true | true | true | true | 1,121 |
4 | INTRODUCTION | 0 | null | null | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | Furthermore, we report a genetic analysis of the roles of the various NS1 domains for such regulation. | null | 102 | 6,864 | 0 | false | null | null | Furthermore, we report a genetic analysis of the roles of the various NS1 domains for such regulation. | true | true | true | true | true | 1,121 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | In this report, we have analysed the consequences of NS1 protein expression in the splicing and nucleo-cytoplasmic transport of NS transcripts using a transient system for the replication and transcription of a recombinant influenza virus NS replicon. | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 251 | 6,865 | 0 | false | In this report, we have analysed the consequences of NS1 protein expression in the splicing and nucleo-cytoplasmic transport of NS transcripts using a transient system for the replication and transcription of a recombinant influenza virus NS replicon. | [] | In this report, we have analysed the consequences of NS1 protein expression in the splicing and nucleo-cytoplasmic transport of NS transcripts using a transient system for the replication and transcription of a recombinant influenza virus NS replicon. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | This is a convenient system that can be used as a model of the situation of an infected cell. | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 93 | 6,866 | 0 | false | This is a convenient system that can be used as a model of the situation of an infected cell. | [] | This is a convenient system that can be used as a model of the situation of an infected cell. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Indeed, the experimental approach used is a development of the amplification in vivo of transcriptionally active viral mini-RNPs employed in the past for structural studies (2,54,55). | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 183 | 6,867 | 0 | false | Indeed, the experimental approach used is a development of the amplification in vivo of transcriptionally active viral mini-RNPs employed in the past for structural studies. | [
"2,54,55"
] | Indeed, the experimental approach used is a development of the amplification in vivo of transcriptionally active viral mini-RNPs employed in the past for structural studies. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Furthermore, full-length RNPs generated in a similar way have been rescued into infectious virus (44,46). | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 105 | 6,868 | 0 | false | Furthermore, full-length RNPs generated in a similar way have been rescued into infectious virus. | [
"44,46"
] | Furthermore, full-length RNPs generated in a similar way have been rescued into infectious virus. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Here we show that NS replicons can be transiently amplified and express both NS1 and NEP(NS2) proteins in proportions and to levels similar to those produced in the virus infection (Figures 2–4). | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 195 | 6,869 | 0 | false | Here we show that NS replicons can be transiently amplified and express both NS1 and NEP proteins in proportions and to levels similar to those produced in the virus infection. | [
"NS2",
"Figures 2–4"
] | Here we show that NS replicons can be transiently amplified and express both NS1 and NEP proteins in proportions and to levels similar to those produced in the virus infection. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | We felt that this should be a convenient system to carry out a genetic analysis of the role of NS1 in the maturation and export of viral transcripts as the studies could be made independent of other possible phenotypes described for NS1 mutants. | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 245 | 6,870 | 0 | false | We felt that this should be a convenient system to carry out a genetic analysis of the role of NS1 in the maturation and export of viral transcripts as the studies could be made independent of other possible phenotypes described for NS1 mutants. | [] | We felt that this should be a convenient system to carry out a genetic analysis of the role of NS1 in the maturation and export of viral transcripts as the studies could be made independent of other possible phenotypes described for NS1 mutants. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Thus, mutants NS1 81 and 11C show predominant alterations in late virus gene expression and particle formation (44,46), aspects not relevant in the experimental setting used here. | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 179 | 6,871 | 0 | false | Thus, mutants NS1 81 and 11C show predominant alterations in late virus gene expression and particle formation, aspects not relevant in the experimental setting used here. | [
"44,46"
] | Thus, mutants NS1 81 and 11C show predominant alterations in late virus gene expression and particle formation, aspects not relevant in the experimental setting used here. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 56 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | On the other hand, a ΔNS1 virus mutant is difficult to handle in a cell line with a normal interferon response (56) but can be studied normally in a transient situation as the one described here. | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 195 | 6,872 | 1 | false | On the other hand, a ΔNS1 virus mutant is difficult to handle in a cell line with a normal interferon response but can be studied normally in a transient situation as the one described here. | [
"56"
] | On the other hand, a ΔNS1 virus mutant is difficult to handle in a cell line with a normal interferon response but can be studied normally in a transient situation as the one described here. | true | true | true | true | true | 1,122 |
0 | DISCUSSION | 1 | 57 | [
"B2",
"B54",
"B55",
"B44",
"B46",
"B44",
"B46",
"B56",
"B57"
] | 17,488,845 | pmid-9135141|pmid-11306552|NA|pmid-291039|pmid-6169001|pmid-7407920|pmid-6945577|NA|pmid-2140629|pmid-3841059|pmid-1710647|pmid-11306552|pmid-10590102|pmid-14691253|pmid-15047804|pmid-16306596|pmid-15047804|pmid-16306596|pmid-9878611|pmid-11312364 | Although it has been reported that the presence of NEP(NS2) protein inhibits viral RNA replication in a similar recombinant system (57), we consider this effect non-relevant to our studies, that deal with the post-transcriptional processing and export of viral mRNAs. | [
"2",
"54",
"55",
"44",
"46",
"44",
"46",
"56",
"57"
] | 267 | 6,873 | 1 | false | Although it has been reported that the presence of NEP protein inhibits viral RNA replication in a similar recombinant system, we consider this effect non-relevant to our studies, that deal with the post-transcriptional processing and export of viral mRNAs. | [
"NS2",
"57"
] | Although it has been reported that the presence of NEP protein inhibits viral RNA replication in a similar recombinant system, we consider this effect non-relevant to our studies, that deal with the post-transcriptional processing and export of viral mRNAs. | true | true | true | true | true | 1,122 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | The results presented here indicate that NS1 protein inhibits the splicing of the NS collinear transcript in a RNA-independent manner, as mutant NS1 R38A/K41A behaves as wt (Figure 6; Table 1), and preferentially blocks the nucleo-cytoplasmic export of NS1 mRNA by a mechanism dependent on NS1–RNA interaction, since mut... | [
"19",
"30",
"31"
] | 399 | 6,874 | 0 | false | The results presented here indicate that NS1 protein inhibits the splicing of the NS collinear transcript in a RNA-independent manner, as mutant NS1 R38A/K41A behaves as wt (Figure 6; Table 1), and preferentially blocks the nucleo-cytoplasmic export of NS1 mRNA by a mechanism dependent on NS1–RNA interaction, since mut... | [] | The results presented here indicate that NS1 protein inhibits the splicing of the NS collinear transcript in a RNA-independent manner, as mutant NS1 R38A/K41A behaves as wt, and preferentially blocks the nucleo-cytoplasmic export of NS1 mRNA by a mechanism dependent on NS1–RNA interaction, since mutant NS1 R38A/K41A pe... | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | Although cells in which a mutant NS R38A/K41A has been established accumulate large amounts of NS1 mRNA and very little NEP(NS2) mRNA in their cytoplasms (Figures 6 and 7), quasi-normal synthesis of NEP(NS2) protein is produced (Figures 2 and 3B). | [
"19",
"30",
"31"
] | 247 | 6,875 | 0 | false | Although cells in which a mutant NS R38A/K41A has been established accumulate large amounts of NS1 mRNA and very little NEP(NS2) mRNA in their cytoplasms (Figures 6 and 7), quasi-normal synthesis of NEP(NS2) protein is produced (Figures 2 and 3B). | [] | Although cells in which a mutant NS R38A/K41A has been established accumulate large amounts of NS1 mRNA and very little NEP(NS2) mRNA in their cytoplasms (Figures 6 and 7), quasi-normal synthesis of NEP(NS2) protein is produced (Figures 2 and 3B). | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | This apparent contradiction can be explained by the fact that, at early times in the replication and transcription of the NS R38A/K41A replicon, no NS1 protein is present in the system. | [
"19",
"30",
"31"
] | 185 | 6,876 | 0 | false | This apparent contradiction can be explained by the fact that, at early times in the replication and transcription of the NS R38A/K41A replicon, no NS1 protein is present in the system. | [] | This apparent contradiction can be explained by the fact that, at early times in the replication and transcription of the NS R38A/K41A replicon, no NS1 protein is present in the system. | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | Until NS1 protein is accumulated to the required intracellular levels, efficient splicing of the collinear transcript is to be expected, as this is the situation with a NS ΔNS1 replicon (Figure 6). | [
"19",
"30",
"31"
] | 197 | 6,877 | 0 | false | Until NS1 protein is accumulated to the required intracellular levels, efficient splicing of the collinear transcript is to be expected, as this is the situation with a NS ΔNS1 replicon (Figure 6). | [] | Until NS1 protein is accumulated to the required intracellular levels, efficient splicing of the collinear transcript is to be expected, as this is the situation with a NS ΔNS1 replicon (Figure 6). | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | Nevertheless, to account for the observed levels of NEP(NS2) synthesis it would be necessary to invoke a preferential translation of NEP(NS2) mRNA. | [
"19",
"30",
"31"
] | 147 | 6,878 | 0 | false | Nevertheless, to account for the observed levels of NEP(NS2) synthesis it would be necessary to invoke a preferential translation of NEP(NS2) mRNA. | [] | Nevertheless, to account for the observed levels of NEP(NS2) synthesis it would be necessary to invoke a preferential translation of NEP(NS2) mRNA. | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | It is conceivable that NEP(NS2) mRNA is efficiently incorporated into the cell translation machinery because it is generated at the early phase of the replicon gene expression. | [
"19",
"30",
"31"
] | 176 | 6,879 | 0 | false | It is conceivable that NEP(NS2) mRNA is efficiently incorporated into the cell translation machinery because it is generated at the early phase of the replicon gene expression. | [] | It is conceivable that NEP(NS2) mRNA is efficiently incorporated into the cell translation machinery because it is generated at the early phase of the replicon gene expression. | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | On the contrary, NS1 mRNA is produced at later times, when NS1 protein has accumulated. | [
"19",
"30",
"31"
] | 87 | 6,880 | 0 | false | On the contrary, NS1 mRNA is produced at later times, when NS1 protein has accumulated. | [] | On the contrary, NS1 mRNA is produced at later times, when NS1 protein has accumulated. | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | At that point a large fraction of the cell-derived mRNA is being used for virus-induced cap-snatching and incorporation of new mRNAs into the cell translation machinery might be affected. | [
"19",
"30",
"31"
] | 187 | 6,881 | 0 | false | At that point a large fraction of the cell-derived mRNA is being used for virus-induced cap-snatching and incorporation of new mRNAs into the cell translation machinery might be affected. | [] | At that point a large fraction of the cell-derived mRNA is being used for virus-induced cap-snatching and incorporation of new mRNAs into the cell translation machinery might be affected. | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | In addition, the level of NS1 protein present in each setting may influence the translation ability of the NEP mRNA present (19,30,31). | [
"19",
"30",
"31"
] | 135 | 6,882 | 0 | false | In addition, the level of NS1 protein present in each setting may influence the translation ability of the NEP mRNA present. | [
"19,30,31"
] | In addition, the level of NS1 protein present in each setting may influence the translation ability of the NEP mRNA present. | true | true | true | true | true | 1,123 |
1 | DISCUSSION | 1 | 19 | [
"B19",
"B30",
"B31"
] | 17,488,845 | pmid-11162793|pmid-12758165|NA|pmid-7233830|pmid-6328745|pmid-2933634|pmid-2969057|pmid-7884890|pmid-10325410|pmid-1469370|pmid-10024172|pmid-9152423|pmid-9336457|pmid-7908060|pmid-7489502|pmid-9336457|pmid-14967035|pmid-8139028|pmid-9349463|pmid-10325410|NA|pmid-14645908|pmid-10022908|pmid-9651582|pmid-10205180|pmid-9... | Thus, when NS1 is not expressed (ΔNS1 replicon), translation of NEP mRNA might be much less efficient than in those cases in which NS1 protein is abundantly expressed, as for instance in cells harbouring the wt NS replicon. | [
"19",
"30",
"31"
] | 223 | 6,883 | 0 | false | Thus, when NS1 is not expressed (ΔNS1 replicon), translation of NEP mRNA might be much less efficient than in those cases in which NS1 protein is abundantly expressed, as for instance in cells harbouring the wt NS replicon. | [] | Thus, when NS1 is not expressed, translation of NEP mRNA might be much less efficient than in those cases in which NS1 protein is abundantly expressed, as for instance in cells harbouring the wt NS replicon. | true | true | true | true | true | 1,123 |
2 | DISCUSSION | 1 | 26 | [
"B26",
"B40",
"B40",
"B41",
"B33",
"B42",
"B40",
"B58"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | The effects of NS1 in the splicing and nucleo-cytoplasmic transport of mRNAs have been studied previously by several groups, including ours, but the analyses were carried out in vitro or using as targets cellular mRNAs or viral ORFs expressed as RNA polymerase II transcripts, but not true virus transcripts. | [
"26",
"40",
"40",
"41",
"33",
"42",
"40",
"58"
] | 308 | 6,884 | 0 | false | The effects of NS1 in the splicing and nucleo-cytoplasmic transport of mRNAs have been studied previously by several groups, including ours, but the analyses were carried out in vitro or using as targets cellular mRNAs or viral ORFs expressed as RNA polymerase II transcripts, but not true virus transcripts. | [] | The effects of NS1 in the splicing and nucleo-cytoplasmic transport of mRNAs have been studied previously by several groups, including ours, but the analyses were carried out in vitro or using as targets cellular mRNAs or viral ORFs expressed as RNA polymerase II transcripts, but not true virus transcripts. | true | true | true | true | true | 1,124 |
2 | DISCUSSION | 1 | 26 | [
"B26",
"B40",
"B40",
"B41",
"B33",
"B42",
"B40",
"B58"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | On the basis of these studies, several models have been put forward along the years for the inhibition of pre-mRNA splicing by NS1: (i) From the results of in vitro experiments it was first proposed that the binding of NS1 to a specific motif in U6 snRNA would impede proper formation of U6-U2 and U6-U4 snRNP interactio... | [
"26",
"40",
"40",
"41",
"33",
"42",
"40",
"58"
] | 378 | 6,885 | 0 | false | On the basis of these studies, several models have been put forward along the years for the inhibition of pre-mRNA splicing by NS1: (i) From the results of in vitro experiments it was first proposed that the binding of NS1 to a specific motif in U6 snRNA would impede proper formation of U6-U2 and U6-U4 snRNP interactio... | [
"26,40"
] | On the basis of these studies, several models have been put forward along the years for the inhibition of pre-mRNA splicing by NS1: (i) From the results of in vitro experiments it was first proposed that the binding of NS1 to a specific motif in U6 snRNA would impede proper formation of U6-U2 and U6-U4 snRNP interactio... | true | true | true | true | true | 1,124 |
2 | DISCUSSION | 1 | 40 | [
"B26",
"B40",
"B40",
"B41",
"B33",
"B42",
"B40",
"B58"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | Such inhibitory interaction was postulated to occur in splicing reactions on cellular pre-mRNAs but not on viral mRNAs (40). | [
"26",
"40",
"40",
"41",
"33",
"42",
"40",
"58"
] | 124 | 6,886 | 1 | false | Such inhibitory interaction was postulated to occur in splicing reactions on cellular pre-mRNAs but not on viral mRNAs. | [
"40"
] | Such inhibitory interaction was postulated to occur in splicing reactions on cellular pre-mRNAs but not on viral mRNAs. | true | true | true | true | true | 1,124 |
2 | DISCUSSION | 1 | 41 | [
"B26",
"B40",
"B40",
"B41",
"B33",
"B42",
"B40",
"B58"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | This model would not explain the alterations induced by NS1 in the use of alternative splice sites (41) and is not supported by the results presented in this report, as we show that NS1 protein indeed inhibits the splicing of a true viral pre-mRNA (the NS collinear transcript) and the RNA-binding activity of NS1 is not... | [
"26",
"40",
"40",
"41",
"33",
"42",
"40",
"58"
] | 361 | 6,887 | 1 | false | This model would not explain the alterations induced by NS1 in the use of alternative splice sites and is not supported by the results presented in this report, as we show that NS1 protein indeed inhibits the splicing of a true viral pre-mRNA (the NS collinear transcript) and the RNA-binding activity of NS1 is not requ... | [
"41"
] | This model would not explain the alterations induced by NS1 in the use of alternative splice sites and is not supported by the results presented in this report, as we show that NS1 protein indeed inhibits the splicing of a true viral pre-mRNA (the NS collinear transcript) and the RNA-binding activity of NS1 is not requ... | true | true | true | true | true | 1,124 |
2 | DISCUSSION | 1 | 33 | [
"B26",
"B40",
"B40",
"B41",
"B33",
"B42",
"B40",
"B58"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | (ii) After reporting that the effector domain of NS1 protein binds the 30 kDa subunit of CPSF and blocks cellular mRNA cleavage and polyadenylation (33), it was proposed that the splicing inhibition by NS1 would be an indirect consequence of the failure in 3′-end processing, as the definition of the exon in a single-ex... | [
"26",
"40",
"40",
"41",
"33",
"42",
"40",
"58"
] | 382 | 6,888 | 1 | false | (ii) After reporting that the effector domain of NS1 protein binds the 30 kDa subunit of CPSF and blocks cellular mRNA cleavage and polyadenylation, it was proposed that the splicing inhibition by NS1 would be an indirect consequence of the failure in 3′-end processing, as the definition of the exon in a single-exon co... | [
"33",
"42"
] | (ii) After reporting that the effector domain of NS1 protein binds the 30 kDa subunit of CPSF and blocks cellular mRNA cleavage and polyadenylation, it was proposed that the splicing inhibition by NS1 would be an indirect consequence of the failure in 3′-end processing, as the definition of the exon in a single-exon co... | false | false | true | true | false | 1,124 |
2 | DISCUSSION | 1 | 40 | [
"B26",
"B40",
"B40",
"B41",
"B33",
"B42",
"B40",
"B58"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | This model would explain the inhibition of cellular mRNA splicing and the lack of such inhibition for intron-containing viral mRNAs (40), since the 3′-polyadenylation of the latter is carried out by polymerase stuttering (58). | [
"26",
"40",
"40",
"41",
"33",
"42",
"40",
"58"
] | 226 | 6,889 | 1 | false | This model would explain the inhibition of cellular mRNA splicing and the lack of such inhibition for intron-containing viral mRNAs, since the 3′-polyadenylation of the latter is carried out by polymerase stuttering. | [
"40",
"58"
] | This model would explain the inhibition of cellular mRNA splicing and the lack of such inhibition for intron-containing viral mRNAs, since the 3′-polyadenylation of the latter is carried out by polymerase stuttering. | true | true | true | true | true | 1,124 |
2 | DISCUSSION | 1 | 26 | [
"B26",
"B40",
"B40",
"B41",
"B33",
"B42",
"B40",
"B58"
] | 17,488,845 | pmid-3461442|pmid-2522588|pmid-1532050|pmid-6328745|pmid-3023072|pmid-7958859|pmid-8313914|pmid-7489502|pmid-7958859|pmid-7958859|pmid-8313914|pmid-9651582|pmid-11421366|pmid-7958859|pmid-10074205 | Again, our results do not support the proposed model, as NS1 protein indeed blocks the splicing of the NS collinear transcript and a NS1 mutant lacking the effector domain fully inhibits the splicing of its own mRNA (Figure 6). | [
"26",
"40",
"40",
"41",
"33",
"42",
"40",
"58"
] | 227 | 6,890 | 0 | false | Again, our results do not support the proposed model, as NS1 protein indeed blocks the splicing of the NS collinear transcript and a NS1 mutant lacking the effector domain fully inhibits the splicing of its own mRNA (Figure 6). | [] | Again, our results do not support the proposed model, as NS1 protein indeed blocks the splicing of the NS collinear transcript and a NS1 mutant lacking the effector domain fully inhibits the splicing of its own mRNA. | true | true | true | true | true | 1,124 |
3 | DISCUSSION | 1 | 35 | [
"B35",
"B41",
"B59",
"B60"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-11421366|pmid-9696811|pmid-8313914|pmid-9049349|pmid-12667806 | We cannot rule out the possibility that NS1 inhibition of cellular mRNA 3′-end formation would indirectly affect the splicing of cellular pre-mRNAs, but the results presented here suggest that NS1 protein would inhibit splicing by a more general mechanism. | [
"35",
"41",
"59",
"60"
] | 256 | 6,891 | 0 | false | We cannot rule out the possibility that NS1 inhibition of cellular mRNA 3′-end formation would indirectly affect the splicing of cellular pre-mRNAs, but the results presented here suggest that NS1 protein would inhibit splicing by a more general mechanism. | [] | We cannot rule out the possibility that NS1 inhibition of cellular mRNA 3′-end formation would indirectly affect the splicing of cellular pre-mRNAs, but the results presented here suggest that NS1 protein would inhibit splicing by a more general mechanism. | true | true | true | true | true | 1,125 |
3 | DISCUSSION | 1 | 35 | [
"B35",
"B41",
"B59",
"B60"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-11421366|pmid-9696811|pmid-8313914|pmid-9049349|pmid-12667806 | The interaction with NS1–BP, a human protein involved in splicing (35) is one possibility, while a de-regulation of the phosphorylation state of SR proteins is an alternative that would explain the modification in alternative splice site usage by NS1 expression (41). | [
"35",
"41",
"59",
"60"
] | 267 | 6,892 | 1 | false | The interaction with NS1–BP, a human protein involved in splicing is one possibility, while a de-regulation of the phosphorylation state of SR proteins is an alternative that would explain the modification in alternative splice site usage by NS1 expression. | [
"35",
"41"
] | The interaction with NS1–BP, a human protein involved in splicing is one possibility, while a de-regulation of the phosphorylation state of SR proteins is an alternative that would explain the modification in alternative splice site usage by NS1 expression. | true | true | true | true | true | 1,125 |
3 | DISCUSSION | 1 | 59 | [
"B35",
"B41",
"B59",
"B60"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-11421366|pmid-9696811|pmid-8313914|pmid-9049349|pmid-12667806 | A general inhibition of the splicing machinery would be in line with the changes in the localization of snRNPs induced by NS1 expression or virus infection (59) and could be considered as part of the viral response to inhibit the expression of cellular antiviral factors (60). | [
"35",
"41",
"59",
"60"
] | 276 | 6,893 | 1 | false | A general inhibition of the splicing machinery would be in line with the changes in the localization of snRNPs induced by NS1 expression or virus infection and could be considered as part of the viral response to inhibit the expression of cellular antiviral factors. | [
"59",
"60"
] | A general inhibition of the splicing machinery would be in line with the changes in the localization of snRNPs induced by NS1 expression or virus infection and could be considered as part of the viral response to inhibit the expression of cellular antiviral factors. | true | true | true | true | true | 1,125 |
3 | DISCUSSION | 1 | 35 | [
"B35",
"B41",
"B59",
"B60"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-11421366|pmid-9696811|pmid-8313914|pmid-9049349|pmid-12667806 | Whatever the mechanism involved, our data indicate that inhibition would be mediated by the N-terminal region of NS1 but would not require NS1–RNA interactions (Figure 6). | [
"35",
"41",
"59",
"60"
] | 171 | 6,894 | 0 | false | Whatever the mechanism involved, our data indicate that inhibition would be mediated by the N-terminal region of NS1 but would not require NS1–RNA interactions (Figure 6). | [] | Whatever the mechanism involved, our data indicate that inhibition would be mediated by the N-terminal region of NS1 but would not require NS1–RNA interactions (Figure 6). | true | true | true | true | true | 1,125 |
4 | DISCUSSION | 1 | 33 | [
"B25",
"B28",
"B41",
"B33",
"B34",
"B58",
"B61",
"B33",
"B61",
"B53",
"B62"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | As indicated earlier, the nucleo-cytoplasmic transport of mRNAs is inhibited by expression of NS1 from cloned DNA (25,28,41) and a model has been proposed for such inhibition based upon the interaction of NS1 with the 30 kDa subunit of the CPSF and the subsequent inhibition of 3′-end mRNA processing (33). | [
"25",
"28",
"41",
"33",
"34",
"58",
"61",
"33",
"61",
"53",
"62"
] | 306 | 6,895 | 1 | false | As indicated earlier, the nucleo-cytoplasmic transport of mRNAs is inhibited by expression of NS1 from cloned DNA and a model has been proposed for such inhibition based upon the interaction of NS1 with the 30 kDa subunit of the CPSF and the subsequent inhibition of 3′-end mRNA processing. | [
"25,28,41",
"33"
] | As indicated earlier, the nucleo-cytoplasmic transport of mRNAs is inhibited by expression of NS1 from cloned DNA and a model has been proposed for such inhibition based upon the interaction of NS1 with the 30 kDa subunit of the CPSF and the subsequent inhibition of 3′-end mRNA processing. | true | true | true | true | true | 1,126 |
4 | DISCUSSION | 1 | 34 | [
"B25",
"B28",
"B41",
"B33",
"B34",
"B58",
"B61",
"B33",
"B61",
"B53",
"B62"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | In addition, the interaction of NS1 with nuclear PABPII would block the export of mRNAs that could partially escape from the inhibition of 3′-end formation (34). | [
"25",
"28",
"41",
"33",
"34",
"58",
"61",
"33",
"61",
"53",
"62"
] | 161 | 6,896 | 1 | false | In addition, the interaction of NS1 with nuclear PABPII would block the export of mRNAs that could partially escape from the inhibition of 3′-end formation. | [
"34"
] | In addition, the interaction of NS1 with nuclear PABPII would block the export of mRNAs that could partially escape from the inhibition of 3′-end formation. | true | true | true | true | true | 1,126 |
4 | DISCUSSION | 1 | 58 | [
"B25",
"B28",
"B41",
"B33",
"B34",
"B58",
"B61",
"B33",
"B61",
"B53",
"B62"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | This model suggested that the export of true viral mRNAs would not be affected by this transport block because their poly A-tails are produced by the viral polymerase in a way independent of normal cell mRNA polyadenylation (58). | [
"25",
"28",
"41",
"33",
"34",
"58",
"61",
"33",
"61",
"53",
"62"
] | 229 | 6,897 | 1 | false | This model suggested that the export of true viral mRNAs would not be affected by this transport block because their poly A-tails are produced by the viral polymerase in a way independent of normal cell mRNA polyadenylation. | [
"58"
] | This model suggested that the export of true viral mRNAs would not be affected by this transport block because their poly A-tails are produced by the viral polymerase in a way independent of normal cell mRNA polyadenylation. | true | true | true | true | true | 1,126 |
4 | DISCUSSION | 1 | 61 | [
"B25",
"B28",
"B41",
"B33",
"B34",
"B58",
"B61",
"B33",
"B61",
"B53",
"B62"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | In addition, the interaction of NS1 with the TAP/p15 pathway for mRNA export has been recently described (61), leading to the block of transport of cellular mRNAs that have undergone splicing. | [
"25",
"28",
"41",
"33",
"34",
"58",
"61",
"33",
"61",
"53",
"62"
] | 192 | 6,898 | 1 | false | In addition, the interaction of NS1 with the TAP/p15 pathway for mRNA export has been recently described, leading to the block of transport of cellular mRNAs that have undergone splicing. | [
"61"
] | In addition, the interaction of NS1 with the TAP/p15 pathway for mRNA export has been recently described, leading to the block of transport of cellular mRNAs that have undergone splicing. | true | true | true | true | true | 1,126 |
4 | DISCUSSION | 1 | 25 | [
"B25",
"B28",
"B41",
"B33",
"B34",
"B58",
"B61",
"B33",
"B61",
"B53",
"B62"
] | 17,488,845 | pmid-7908060|pmid-8139028|pmid-8313914|pmid-9651582|pmid-10205180|pmid-10074205|pmid-17267598|pmid-9651582|pmid-17267598|pmid-17132145|pmid-12791298 | However, the results shown in this report indicate that a preferential block of NS1 mRNA export is produced when NS1 is expressed from a NS replicon and further suggest that the RNA-binding activity of NS1 is required for the inhibition of viral mRNA export (Figure 7). | [
"25",
"28",
"41",
"33",
"34",
"58",
"61",
"33",
"61",
"53",
"62"
] | 269 | 6,899 | 0 | false | However, the results shown in this report indicate that a preferential block of NS1 mRNA export is produced when NS1 is expressed from a NS replicon and further suggest that the RNA-binding activity of NS1 is required for the inhibition of viral mRNA export (Figure 7). | [] | However, the results shown in this report indicate that a preferential block of NS1 mRNA export is produced when NS1 is expressed from a NS replicon and further suggest that the RNA-binding activity of NS1 is required for the inhibition of viral mRNA export (Figure 7). | true | true | true | true | true | 1,126 |
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