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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0 | DISCUSSION | 1 | 17 | [
"B17",
"B19",
"B20",
"B22"
] | 18,676,978 | NA|pmid-15269332|pmid-17105995|pmid-12955455|pmid-17295027|pmid-14960277|pmid-12080340|pmid-17217467|pmid-16326926 | We demonstrate that ZmWHY1 is essential for chloroplast biogenesis, and that it localizes to the chloroplast where it plays multiple roles in gene expression. | [
"17",
"19",
"20",
"22"
] | 158 | 41,619 | 0 | false | We demonstrate that ZmWHY1 is essential for chloroplast biogenesis, and that it localizes to the chloroplast where it plays multiple roles in gene expression. | [] | We demonstrate that ZmWHY1 is essential for chloroplast biogenesis, and that it localizes to the chloroplast where it plays multiple roles in gene expression. | true | true | true | true | true | 7,177 |
0 | DISCUSSION | 1 | 17 | [
"B17",
"B19",
"B20",
"B22"
] | 18,676,978 | NA|pmid-15269332|pmid-17105995|pmid-12955455|pmid-17295027|pmid-14960277|pmid-12080340|pmid-17217467|pmid-16326926 | We also add RNA binding to WHY1's repertoire of biochemical activities and demonstrate that ZmWHY1 is bound to a subset of chloroplast RNAs in chloroplast extract. | [
"17",
"19",
"20",
"22"
] | 163 | 41,620 | 0 | false | We also add RNA binding to WHY1's repertoire of biochemical activities and demonstrate that ZmWHY1 is bound to a subset of chloroplast RNAs in chloroplast extract. | [] | We also add RNA binding to WHY1's repertoire of biochemical activities and demonstrate that ZmWHY1 is bound to a subset of chloroplast RNAs in chloroplast extract. | true | true | true | true | true | 7,177 |
1 | DISCUSSION | 0 | null | null | 18,676,978 | pmid-9090875|pmid-11179231|pmid-18065687|pmid-17071648|pmid-12881426|pmid-11565746|pmid-17693527|NA|NA|pmid-17041147|pmid-9090875|pmid-17071648|pmid-12881426|pmid-11565746|pmid-15598799 | ZmWHY was identified among proteins that coimmunoprecipitate with CRS1, which is required for the splicing of the group II intron in the chloroplast atpF pre-mRNA. | null | 163 | 41,621 | 0 | false | null | null | ZmWHY was identified among proteins that coimmunoprecipitate with CRS1, which is required for the splicing of the group II intron in the chloroplast atpF pre-mRNA. | true | true | true | true | true | 7,178 |
1 | DISCUSSION | 0 | null | null | 18,676,978 | pmid-9090875|pmid-11179231|pmid-18065687|pmid-17071648|pmid-12881426|pmid-11565746|pmid-17693527|NA|NA|pmid-17041147|pmid-9090875|pmid-17071648|pmid-12881426|pmid-11565746|pmid-15598799 | We showed that ZmWHY1 is associated with atpF intron RNA in vivo and that the coimmunoprecipitation of ZmWHY1 and CRS1 is disrupted by RNAse, indicating that they coimmunoprecipitate due to their association with the same RNA molecule. | null | 235 | 41,622 | 0 | false | null | null | We showed that ZmWHY1 is associated with atpF intron RNA in vivo and that the coimmunoprecipitation of ZmWHY1 and CRS1 is disrupted by RNAse, indicating that they coimmunoprecipitate due to their association with the same RNA molecule. | true | true | true | true | true | 7,178 |
1 | DISCUSSION | 0 | null | null | 18,676,978 | pmid-9090875|pmid-11179231|pmid-18065687|pmid-17071648|pmid-12881426|pmid-11565746|pmid-17693527|NA|NA|pmid-17041147|pmid-9090875|pmid-17071648|pmid-12881426|pmid-11565746|pmid-15598799 | ZmWHY1's association with atpF RNA is functionally significant, as atpF intron splicing is disrupted in ZmWhy1 mutants. | null | 119 | 41,623 | 0 | false | null | null | ZmWHY1's association with atpF RNA is functionally significant, as atpF intron splicing is disrupted in ZmWhy1 mutants. | true | true | true | true | true | 7,178 |
1 | DISCUSSION | 0 | null | null | 18,676,978 | pmid-9090875|pmid-11179231|pmid-18065687|pmid-17071648|pmid-12881426|pmid-11565746|pmid-17693527|NA|NA|pmid-17041147|pmid-9090875|pmid-17071648|pmid-12881426|pmid-11565746|pmid-15598799 | However, the splicing of this intron is more sensitive to a partial loss of CRS1 than to a partial loss of ZmWHY1, suggesting that ZmWHY1 plays an accessory function in atpF splicing but may not be absolutely required. | null | 218 | 41,624 | 0 | false | null | null | However, the splicing of this intron is more sensitive to a partial loss of CRS1 than to a partial loss of ZmWHY1, suggesting that ZmWHY1 plays an accessory function in atpF splicing but may not be absolutely required. | true | true | true | true | true | 7,178 |
2 | DISCUSSION | 1 | 11 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | The atpF splicing defect in ZmWhy1 mutants cannot account for their loss of plastid ribosomes, as the more severe atpF splicing defect in crs1-1 mutants is not accompanied by a substantial plastid ribosome deficiency (11). | [
"11",
"39",
"43–46"
] | 222 | 41,625 | 1 | false | The atpF splicing defect in ZmWhy1 mutants cannot account for their loss of plastid ribosomes, as the more severe atpF splicing defect in crs1-1 mutants is not accompanied by a substantial plastid ribosome deficiency. | [
"11"
] | The atpF splicing defect in ZmWhy1 mutants cannot account for their loss of plastid ribosomes, as the more severe atpF splicing defect in crs1-1 mutants is not accompanied by a substantial plastid ribosome deficiency. | true | true | true | true | true | 7,179 |
2 | DISCUSSION | 1 | 11 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | The specific role of ZmWHY1 in promoting the biogenesis of the plastid translation machinery remains unclear. | [
"11",
"39",
"43–46"
] | 109 | 41,626 | 0 | false | The specific role of ZmWHY1 in promoting the biogenesis of the plastid translation machinery remains unclear. | [] | The specific role of ZmWHY1 in promoting the biogenesis of the plastid translation machinery remains unclear. | true | true | true | true | true | 7,179 |
2 | DISCUSSION | 1 | 11 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | Although several RNAs with translation-related functions are among the RNAs that coimmunoprecipitate with ZmWHY1, the abundance and processing of these RNAs are similar in ZmWhy1 mutants and in control mutants that exhibit a ribosome-deficiency of similar severity. | [
"11",
"39",
"43–46"
] | 265 | 41,627 | 0 | false | Although several RNAs with translation-related functions are among the RNAs that coimmunoprecipitate with ZmWHY1, the abundance and processing of these RNAs are similar in ZmWhy1 mutants and in control mutants that exhibit a ribosome-deficiency of similar severity. | [] | Although several RNAs with translation-related functions are among the RNAs that coimmunoprecipitate with ZmWHY1, the abundance and processing of these RNAs are similar in ZmWhy1 mutants and in control mutants that exhibit a ribosome-deficiency of similar severity. | true | true | true | true | true | 7,179 |
2 | DISCUSSION | 1 | 11 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | The specific rRNA deficiencies in ZmWhy1 mutants do suggest, however, that ZmWHY1 is most directly involved in the biogenesis of the large ribosomal subunit: the accumulation and processing of the 23S and 4.5S rRNAs are more sensitive to the partial loss of ZmWhy1 function than are those of 16S rRNA, whereas the revers... | [
"11",
"39",
"43–46"
] | 347 | 41,628 | 0 | false | The specific rRNA deficiencies in ZmWhy1 mutants do suggest, however, that ZmWHY1 is most directly involved in the biogenesis of the large ribosomal subunit: the accumulation and processing of the 23S and 4.5S rRNAs are more sensitive to the partial loss of ZmWhy1 function than are those of 16S rRNA, whereas the revers... | [] | The specific rRNA deficiencies in ZmWhy1 mutants do suggest, however, that ZmWHY1 is most directly involved in the biogenesis of the large ribosomal subunit: the accumulation and processing of the 23S and 4.5S rRNAs are more sensitive to the partial loss of ZmWhy1 function than are those of 16S rRNA, whereas the revers... | true | true | true | true | true | 7,179 |
2 | DISCUSSION | 1 | 39 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | Furthermore, in ppr5 mutants, whose primary defect is in the maturation of a specific plastid tRNA, the rRNAs from the two ribosomal subunits are impacted to a similar extent (39). | [
"11",
"39",
"43–46"
] | 180 | 41,629 | 1 | false | Furthermore, in ppr5 mutants, whose primary defect is in the maturation of a specific plastid tRNA, the rRNAs from the two ribosomal subunits are impacted to a similar extent. | [
"39"
] | Furthermore, in ppr5 mutants, whose primary defect is in the maturation of a specific plastid tRNA, the rRNAs from the two ribosomal subunits are impacted to a similar extent. | true | true | true | true | true | 7,179 |
2 | DISCUSSION | 1 | 11 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | Thus, our results point to the biogenesis of the plastid large ribosomal subunit as one function of ZmWHY1 but definition of its precise role in this process will require additional study. | [
"11",
"39",
"43–46"
] | 188 | 41,630 | 0 | false | Thus, our results point to the biogenesis of the plastid large ribosomal subunit as one function of ZmWHY1 but definition of its precise role in this process will require additional study. | [] | Thus, our results point to the biogenesis of the plastid large ribosomal subunit as one function of ZmWHY1 but definition of its precise role in this process will require additional study. | true | true | true | true | true | 7,179 |
2 | DISCUSSION | 1 | 43–46 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | The strong defect in the processing step that separates 23S rRNA from 4.5S rRNA in hypomorphic ZmWhy1 mutants is reminiscent of defects reported for mutations in the DCL, DAL and RNR1 genes in dicots (43–46). | [
"11",
"39",
"43–46"
] | 208 | 41,631 | 1 | false | The strong defect in the processing step that separates 23S rRNA from 4.5S rRNA in hypomorphic ZmWhy1 mutants is reminiscent of defects reported for mutations in the DCL, DAL and RNR1 genes in dicots. | [
"43–46"
] | The strong defect in the processing step that separates 23S rRNA from 4.5S rRNA in hypomorphic ZmWhy1 mutants is reminiscent of defects reported for mutations in the DCL, DAL and RNR1 genes in dicots. | true | true | true | true | true | 7,179 |
2 | DISCUSSION | 1 | 11 | [
"B11",
"B39",
"B43 B44 B45 B46"
] | 18,676,978 | pmid-14960277|pmid-10948264|pmid-14960277|pmid-12080340|pmid-17217467|pmid-15967440|pmid-16326926|pmid-18423020|pmid-11565746|NA|pmid-15891117|pmid-15010617|pmid-15197595|pmid-12678554 | Although it is unclear whether any of these genes function directly in 23S/4.5S rRNA processing, it is possible that WHY1 acts in concert with one or more of these proteins. | [
"11",
"39",
"43–46"
] | 173 | 41,632 | 0 | false | Although it is unclear whether any of these genes function directly in 23S/4.5S rRNA processing, it is possible that WHY1 acts in concert with one or more of these proteins. | [] | Although it is unclear whether any of these genes function directly in 23S/4.5S rRNA processing, it is possible that WHY1 acts in concert with one or more of these proteins. | true | true | true | true | true | 7,179 |
3 | DISCUSSION | 1 | 19 | [
"B19",
"B20",
"B22",
"B23"
] | 18,676,978 | pmid-12080340|pmid-17217467|pmid-16326926|pmid-18423020 | We show here that chloroplast DNA coimmunoprecipitates with ZmWHY1 from plastid extract, that a fraction of ZmWHY1 is tethered to the thylakoid membrane in a DNA-dependent fashion, that a fraction of stromal ZmWHY1 is found in DNA-containing particles of ∼400 kDa, and that ZmWHY1 binds ssDNA in vitro. | [
"19",
"20",
"22",
"23"
] | 302 | 41,633 | 0 | false | We show here that chloroplast DNA coimmunoprecipitates with ZmWHY1 from plastid extract, that a fraction of ZmWHY1 is tethered to the thylakoid membrane in a DNA-dependent fashion, that a fraction of stromal ZmWHY1 is found in DNA-containing particles of ∼400 kDa, and that ZmWHY1 binds ssDNA in vitro. | [] | We show here that chloroplast DNA coimmunoprecipitates with ZmWHY1 from plastid extract, that a fraction of ZmWHY1 is tethered to the thylakoid membrane in a DNA-dependent fashion, that a fraction of stromal ZmWHY1 is found in DNA-containing particles of ∼400 kDa, and that ZmWHY1 binds ssDNA in vitro. | true | true | true | true | true | 7,180 |
3 | DISCUSSION | 1 | 22 | [
"B19",
"B20",
"B22",
"B23"
] | 18,676,978 | pmid-12080340|pmid-17217467|pmid-16326926|pmid-18423020 | These results are consistent with previous reports that dicot WHY1 binds ssDNA (19,20) and that it copurifies with a chloroplast ‘transcriptionally active chromosome’ (22). | [
"19",
"20",
"22",
"23"
] | 172 | 41,634 | 1 | false | These results are consistent with previous reports that dicot WHY1 binds ssDNA and that it copurifies with a chloroplast ‘transcriptionally active chromosome’. | [
"19,20",
"22"
] | These results are consistent with previous reports that dicot WHY1 binds ssDNA and that it copurifies with a chloroplast ‘transcriptionally active chromosome’. | true | true | true | true | true | 7,180 |
3 | DISCUSSION | 1 | 19 | [
"B19",
"B20",
"B22",
"B23"
] | 18,676,978 | pmid-12080340|pmid-17217467|pmid-16326926|pmid-18423020 | Our findings suggest that ZmWHY1 either binds DNA in a sequence non-specific fashion or that it has many binding sites distributed throughout the plastid genome, because DNA sequences from throughout the plastid genome coimmunoprecipitated to a similar extent with ZmWHY1. | [
"19",
"20",
"22",
"23"
] | 272 | 41,635 | 0 | false | Our findings suggest that ZmWHY1 either binds DNA in a sequence non-specific fashion or that it has many binding sites distributed throughout the plastid genome, because DNA sequences from throughout the plastid genome coimmunoprecipitated to a similar extent with ZmWHY1. | [] | Our findings suggest that ZmWHY1 either binds DNA in a sequence non-specific fashion or that it has many binding sites distributed throughout the plastid genome, because DNA sequences from throughout the plastid genome coimmunoprecipitated to a similar extent with ZmWHY1. | true | true | true | true | true | 7,180 |
3 | DISCUSSION | 1 | 19 | [
"B19",
"B20",
"B22",
"B23"
] | 18,676,978 | pmid-12080340|pmid-17217467|pmid-16326926|pmid-18423020 | It remains possible, however, that ZmWHY1 associates with specific DNA regions in vivo, but that these associations were disrupted during lysate preparation. | [
"19",
"20",
"22",
"23"
] | 157 | 41,636 | 0 | false | It remains possible, however, that ZmWHY1 associates with specific DNA regions in vivo, but that these associations were disrupted during lysate preparation. | [] | It remains possible, however, that ZmWHY1 associates with specific DNA regions in vivo, but that these associations were disrupted during lysate preparation. | true | true | true | true | true | 7,180 |
3 | DISCUSSION | 1 | 23 | [
"B19",
"B20",
"B22",
"B23"
] | 18,676,978 | pmid-12080340|pmid-17217467|pmid-16326926|pmid-18423020 | A DNA immunoprecipitation experiment was recently reported for AtWHY2, a mitochondrial-localized Whirly protein (23), with analogous results: DNA sequences from a variety of regions throughout the mitochondrial genome coimmunoprecipitated with AtWHY2, when assayed by PCR. | [
"19",
"20",
"22",
"23"
] | 272 | 41,637 | 1 | false | A DNA immunoprecipitation experiment was recently reported for AtWHY2, a mitochondrial-localized Whirly protein, with analogous results: DNA sequences from a variety of regions throughout the mitochondrial genome coimmunoprecipitated with AtWHY2, when assayed by PCR. | [
"23"
] | A DNA immunoprecipitation experiment was recently reported for AtWHY2, a mitochondrial-localized Whirly protein, with analogous results: DNA sequences from a variety of regions throughout the mitochondrial genome coimmunoprecipitated with AtWHY2, when assayed by PCR. | true | true | true | true | true | 7,180 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 18,676,978 | pmid-16923390 | We demonstrate here that ZmWHY1 interacts not only with DNA, as anticipated by previous reports, but that it also binds RNA in vivo and in vitro. | [
"42"
] | 145 | 41,638 | 0 | false | We demonstrate here that ZmWHY1 interacts not only with DNA, as anticipated by previous reports, but that it also binds RNA in vivo and in vitro. | [] | We demonstrate here that ZmWHY1 interacts not only with DNA, as anticipated by previous reports, but that it also binds RNA in vivo and in vitro. | true | true | true | true | true | 7,181 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 18,676,978 | pmid-16923390 | That ZmWHY1 interacts with RNA is, perhaps, not surprising given that a structural homolog of ZmWHY1 has been shown to bind RNAs involved in kinetoplastid RNA editing (42), and that many proteins that bind ssDNA also bind RNA. | [
"42"
] | 226 | 41,639 | 1 | false | That ZmWHY1 interacts with RNA is, perhaps, not surprising given that a structural homolog of ZmWHY1 has been shown to bind RNAs involved in kinetoplastid RNA editing, and that many proteins that bind ssDNA also bind RNA. | [
"42"
] | That ZmWHY1 interacts with RNA is, perhaps, not surprising given that a structural homolog of ZmWHY1 has been shown to bind RNAs involved in kinetoplastid RNA editing, and that many proteins that bind ssDNA also bind RNA. | true | true | true | true | true | 7,181 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 18,676,978 | pmid-16923390 | The atpF intron RNA was the major RNA ligand of ZmWHY1 detected in the RNA coimmunoprecipitation assays. | [
"42"
] | 104 | 41,640 | 0 | false | The atpF intron RNA was the major RNA ligand of ZmWHY1 detected in the RNA coimmunoprecipitation assays. | [] | The atpF intron RNA was the major RNA ligand of ZmWHY1 detected in the RNA coimmunoprecipitation assays. | true | true | true | true | true | 7,181 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 18,676,978 | pmid-16923390 | This RNA is not particularly abundant in vivo so its enrichment in ZmWHY1 immunoprecipitations likely reflects a specific interaction in vivo. | [
"42"
] | 142 | 41,641 | 0 | false | This RNA is not particularly abundant in vivo so its enrichment in ZmWHY1 immunoprecipitations likely reflects a specific interaction in vivo. | [] | This RNA is not particularly abundant in vivo so its enrichment in ZmWHY1 immunoprecipitations likely reflects a specific interaction in vivo. | true | true | true | true | true | 7,181 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 18,676,978 | pmid-16923390 | Although intrinsic specificity for this RNA did not emerge from in vitro binding assays using the entire intron, a high-affinity site within a large RNA such as the atpF intron (∼800 nt) can be masked in vitro due to the overwhelming number of nonspecific sites available for protein binding. | [
"42"
] | 292 | 41,642 | 0 | false | Although intrinsic specificity for this RNA did not emerge from in vitro binding assays using the entire intron, a high-affinity site within a large RNA such as the atpF intron (∼800 nt) can be masked in vitro due to the overwhelming number of nonspecific sites available for protein binding. | [] | Although intrinsic specificity for this RNA did not emerge from in vitro binding assays using the entire intron, a high-affinity site within a large RNA such as the atpF intron (∼800 nt) can be masked in vitro due to the overwhelming number of nonspecific sites available for protein binding. | true | true | true | true | true | 7,181 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 18,676,978 | pmid-16923390 | Therefore, more detailed studies involving smaller RNA ligands will be required to determine whether ZmWHY1 binds RNA with sequence-specificity or whether it is recruited to the atpF intron via protein–protein interactions. | [
"42"
] | 223 | 41,643 | 0 | false | Therefore, more detailed studies involving smaller RNA ligands will be required to determine whether ZmWHY1 binds RNA with sequence-specificity or whether it is recruited to the atpF intron via protein–protein interactions. | [] | Therefore, more detailed studies involving smaller RNA ligands will be required to determine whether ZmWHY1 binds RNA with sequence-specificity or whether it is recruited to the atpF intron via protein–protein interactions. | true | true | true | true | true | 7,181 |
5 | DISCUSSION | 0 | null | null | 18,676,978 | null | The association of ZmyWHY1 with DNA sequences from throughout the chloroplast genome suggests that it participates in transcription and/or DNA metabolism. | null | 154 | 41,644 | 0 | false | null | null | The association of ZmyWHY1 with DNA sequences from throughout the chloroplast genome suggests that it participates in transcription and/or DNA metabolism. | true | true | true | true | true | 7,182 |
5 | DISCUSSION | 0 | null | null | 18,676,978 | null | However, our results argue against a general role in transcription, as all plastid mRNAs examined accumulate in hypomorphic Zmwhy1 mutants to levels that are comparable to those in the relevant control mutants. | null | 210 | 41,645 | 0 | false | null | null | However, our results argue against a general role in transcription, as all plastid mRNAs examined accumulate in hypomorphic Zmwhy1 mutants to levels that are comparable to those in the relevant control mutants. | true | true | true | true | true | 7,182 |
5 | DISCUSSION | 0 | null | null | 18,676,978 | null | The results of chloroplast transcription runon experiments argue that the preferential loss of 23S rRNA in these mutants is due to aberrant ribosome assembly rather than to reduced rRNA transcription rates. | null | 206 | 41,646 | 0 | false | null | null | The results of chloroplast transcription runon experiments argue that the preferential loss of 23S rRNA in these mutants is due to aberrant ribosome assembly rather than to reduced rRNA transcription rates. | true | true | true | true | true | 7,182 |
5 | DISCUSSION | 0 | null | null | 18,676,978 | null | It remains possible, however, that ZmWHY1 does play a role in chloroplast transcription but that another gene with a partially redundant function serves this purpose in ZmWhy1 mutants. | null | 184 | 41,647 | 0 | false | null | null | It remains possible, however, that ZmWHY1 does play a role in chloroplast transcription but that another gene with a partially redundant function serves this purpose in ZmWhy1 mutants. | true | true | true | true | true | 7,182 |
6 | DISCUSSION | 1 | 47 | [
"B47"
] | 18,676,978 | pmid-17189341 | It is intriguing that ZmWHY1 binds preferentially to DNA in single stranded form because opportunities to interact with ssDNA in vivo are expected to be limited. | [
"47"
] | 161 | 41,648 | 0 | false | It is intriguing that ZmWHY1 binds preferentially to DNA in single stranded form because opportunities to interact with ssDNA in vivo are expected to be limited. | [] | It is intriguing that ZmWHY1 binds preferentially to DNA in single stranded form because opportunities to interact with ssDNA in vivo are expected to be limited. | true | true | true | true | true | 7,183 |
6 | DISCUSSION | 1 | 47 | [
"B47"
] | 18,676,978 | pmid-17189341 | DNA replication, recombination and repair involve the transient occurrence of ssDNA, and torsional stress can induce DNA unwinding. | [
"47"
] | 131 | 41,649 | 0 | false | DNA replication, recombination and repair involve the transient occurrence of ssDNA, and torsional stress can induce DNA unwinding. | [] | DNA replication, recombination and repair involve the transient occurrence of ssDNA, and torsional stress can induce DNA unwinding. | true | true | true | true | true | 7,183 |
6 | DISCUSSION | 1 | 47 | [
"B47"
] | 18,676,978 | pmid-17189341 | The Southern blot data showing that plastid DNA levels are no more than minimally decreased in ZmWhy1 null mutants argue against a central role for ZmWHY1 in DNA replication; however participation of ZmWHY1 in DNA recombination or repair remains possible. | [
"47"
] | 255 | 41,650 | 0 | false | The Southern blot data showing that plastid DNA levels are no more than minimally decreased in ZmWhy1 null mutants argue against a central role for ZmWHY1 in DNA replication; however participation of ZmWHY1 in DNA recombination or repair remains possible. | [] | The Southern blot data showing that plastid DNA levels are no more than minimally decreased in ZmWhy1 null mutants argue against a central role for ZmWHY1 in DNA replication; however participation of ZmWHY1 in DNA recombination or repair remains possible. | true | true | true | true | true | 7,183 |
6 | DISCUSSION | 1 | 47 | [
"B47"
] | 18,676,978 | pmid-17189341 | In fact, the participation of an unrelated ssDNA-binding protein, OSB1, in plant mitochondrial DNA recombination was reported recently (47). | [
"47"
] | 140 | 41,651 | 1 | false | In fact, the participation of an unrelated ssDNA-binding protein, OSB1, in plant mitochondrial DNA recombination was reported recently. | [
"47"
] | In fact, the participation of an unrelated ssDNA-binding protein, OSB1, in plant mitochondrial DNA recombination was reported recently. | true | true | true | true | true | 7,183 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | There are several parallels between our findings with ZmWHY1 and the activities reported for the bacterial protein HU | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 117 | 41,652 | 0 | false | There are several parallels between our findings with ZmWHY1 and the activities reported for the bacterial protein HU | [] | There are several parallels between our findings with ZmWHY1 and the activities reported for the bacterial protein HU | true | true | false | true | false | 7,184 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | HU is associated with the bacterial nucleoid, binds preferentially to DNA with irregular structural features (e.g. | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 114 | 41,653 | 0 | false | HU is associated with the bacterial nucleoid, binds preferentially to DNA with irregular structural features (e.g. | [] | HU is associated with the bacterial nucleoid, binds preferentially to DNA with irregular structural features (e.g. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | single stranded gaps and bulges), and is involved in DNA recombination and repair (48,49). | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 90 | 41,654 | 0 | false | single stranded gaps and bulges), and is involved in DNA recombination and repair. | [
"48,49"
] | single stranded gaps and bulges), and is involved in DNA recombination and repair. | false | true | true | true | false | 7,184 |
7 | DISCUSSION | 1 | 50 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | Despite its high conservation in bacteria and the presence of an HU homolog in a plastid genome in red algae (50), HU homologs are not encoded in the nuclear or plastid genomes of vascular plants (50,51). | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 204 | 41,655 | 1 | false | Despite its high conservation in bacteria and the presence of an HU homolog in a plastid genome in red algae, HU homologs are not encoded in the nuclear or plastid genomes of vascular plants. | [
"50",
"50,51"
] | Despite its high conservation in bacteria and the presence of an HU homolog in a plastid genome in red algae, HU homologs are not encoded in the nuclear or plastid genomes of vascular plants. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | Thus, alternative proteins have presumably been recruited in vascular plants to fulfill the functions performed by HU in the chloroplast's cyanobacterial ancestor. | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 163 | 41,656 | 0 | false | Thus, alternative proteins have presumably been recruited in vascular plants to fulfill the functions performed by HU in the chloroplast's cyanobacterial ancestor. | [] | Thus, alternative proteins have presumably been recruited in vascular plants to fulfill the functions performed by HU in the chloroplast's cyanobacterial ancestor. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 51–53 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | The nucleoid-associated protein sulfite reductase has been suggested to be one such protein (51–53), and perhaps WHY1 is another. | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 129 | 41,657 | 1 | false | The nucleoid-associated protein sulfite reductase has been suggested to be one such protein, and perhaps WHY1 is another. | [
"51–53"
] | The nucleoid-associated protein sulfite reductase has been suggested to be one such protein, and perhaps WHY1 is another. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 54–56 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | HU influences global transcription patterns through its effect on nucleoid architecture, and mediates the formation of DNA loops that repress transcription from specific genes (54–56). | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 184 | 41,658 | 1 | false | HU influences global transcription patterns through its effect on nucleoid architecture, and mediates the formation of DNA loops that repress transcription from specific genes. | [
"54–56"
] | HU influences global transcription patterns through its effect on nucleoid architecture, and mediates the formation of DNA loops that repress transcription from specific genes. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | HU is also an RNA-binding protein, and functions in vivo to repress the translation of the E. coli rpoS mRNA (57,58). | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 117 | 41,659 | 0 | false | HU is also an RNA-binding protein, and functions in vivo to repress the translation of the E. coli rpoS mRNA. | [
"57,58"
] | HU is also an RNA-binding protein, and functions in vivo to repress the translation of the E. coli rpoS mRNA. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | Like HU, ZmWHY1 interacts globally with plastid DNA, but specifically with certain plastid RNAs, and binds preferentially to nucleic acids with single-stranded character. | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 170 | 41,660 | 0 | false | Like HU, ZmWHY1 interacts globally with plastid DNA, but specifically with certain plastid RNAs, and binds preferentially to nucleic acids with single-stranded character. | [] | Like HU, ZmWHY1 interacts globally with plastid DNA, but specifically with certain plastid RNAs, and binds preferentially to nucleic acids with single-stranded character. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | The abundance of several chloroplast mRNAs is increased in ZmWhy1 mutants, consistent with a global repressive role for ZmWHY1 in transcription. | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 144 | 41,661 | 0 | false | The abundance of several chloroplast mRNAs is increased in ZmWhy1 mutants, consistent with a global repressive role for ZmWHY1 in transcription. | [] | The abundance of several chloroplast mRNAs is increased in ZmWhy1 mutants, consistent with a global repressive role for ZmWHY1 in transcription. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 23 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | This possibility is in accord with the recent report that over-expression of AtWHY2 in Arabidopsis causes a reduction in the levels of several mitochondrial RNAs (23). | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 167 | 41,662 | 1 | false | This possibility is in accord with the recent report that over-expression of AtWHY2 in Arabidopsis causes a reduction in the levels of several mitochondrial RNAs. | [
"23"
] | This possibility is in accord with the recent report that over-expression of AtWHY2 in Arabidopsis causes a reduction in the levels of several mitochondrial RNAs. | true | true | true | true | true | 7,184 |
7 | DISCUSSION | 1 | 48 | [
"B48",
"B49",
"B50",
"B50",
"B51",
"B51 B52 B53",
"B54 B55 B56",
"B57",
"B58",
"B23"
] | 18,676,978 | pmid-12672495|pmid-18096614|pmid-12119376|pmid-12119376|pmid-11286919|pmid-11286919|pmid-11163356|pmid-17371503|pmid-14500788|pmid-16258062|pmid-10027963|pmid-12006568|pmid-11251825|pmid-18423020 | Although its role in DNA metabolism remains uncertain, our results demonstrate that description of WHY1 as a chloroplast transcription factor is, at best, an over-simplification of the complex roles played by this interesting protein. | [
"48",
"49",
"50",
"50",
"51",
"51–53",
"54–56",
"57",
"58",
"23"
] | 234 | 41,663 | 0 | false | Although its role in DNA metabolism remains uncertain, our results demonstrate that description of WHY1 as a chloroplast transcription factor is, at best, an over-simplification of the complex roles played by this interesting protein. | [] | Although its role in DNA metabolism remains uncertain, our results demonstrate that description of WHY1 as a chloroplast transcription factor is, at best, an over-simplification of the complex roles played by this interesting protein. | true | true | true | true | true | 7,184 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 19,654,939 | pmid-16631505|pmid-17684150|pmid-17884367|pmid-11755373 | Atherosclerotic plaque progression may lead to coronary artery disease (1), stroke (2), peripheral artery disease (3), and sudden cardiac death (SCD) (4) in humans. | [
"1",
"2",
"3",
"4"
] | 164 | 41,664 | 1 | false | Atherosclerotic plaque progression may lead to coronary artery disease, stroke, peripheral artery disease, and sudden cardiac death (SCD) in humans. | [
"1",
"2",
"3",
"4"
] | Atherosclerotic plaque progression may lead to coronary artery disease, stroke, peripheral artery disease, and sudden cardiac death (SCD) in humans. | true | true | true | true | true | 7,185 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 19,654,939 | pmid-16631505|pmid-17684150|pmid-17884367|pmid-11755373 | However, the mechanism of plaque growth, destabilization, and rupture has not been fully established. | [
"1",
"2",
"3",
"4"
] | 101 | 41,665 | 0 | false | However, the mechanism of plaque growth, destabilization, and rupture has not been fully established. | [] | However, the mechanism of plaque growth, destabilization, and rupture has not been fully established. | true | true | true | true | true | 7,185 |
1 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 19,654,939 | pmid-11021830|pmid-11254922|pmid-16801474|pmid-17082488|pmid-17659199|pmid-17729343|pmid-17101043|pmid-17585387|pmid-16814652|pmid-16487837|pmid-16631508|pmid-16781367|pmid-12390948|pmid-15640160 | Atherosclerotic plaque assessment has been conducted in the past using histopathology in autopsy specimens (5, 6). | [
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"12",
"13",
"14",
"15",
"16",
"17"
] | 114 | 41,666 | 0 | false | Atherosclerotic plaque assessment has been conducted in the past using histopathology in autopsy specimens. | [
"5, 6"
] | Atherosclerotic plaque assessment has been conducted in the past using histopathology in autopsy specimens. | true | true | true | true | true | 7,186 |
1 | INTRODUCTION | 1 | 9 | [
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 19,654,939 | pmid-11021830|pmid-11254922|pmid-16801474|pmid-17082488|pmid-17659199|pmid-17729343|pmid-17101043|pmid-17585387|pmid-16814652|pmid-16487837|pmid-16631508|pmid-16781367|pmid-12390948|pmid-15640160 | Recently, serum biomarker studies (7, 8) and imaging studies such as computerized tomography (9), magnetic resonance imaging (10), intima-media thickness (11), coronary angiography (12), optical coherence tomography (13), intravascular ultrasound (IVUS) (14, 15), and virtual histology IVUS (VH-IVUS) (16, 17) have been ... | [
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"12",
"13",
"14",
"15",
"16",
"17"
] | 343 | 41,667 | 1 | false | Recently, serum biomarker studies and imaging studies such as computerized tomography, magnetic resonance imaging, intima-media thickness, coronary angiography, optical coherence tomography, intravascular ultrasound (IVUS), and virtual histology IVUS (VH-IVUS) have been used to assess plaques. | [
"7, 8",
"9",
"10",
"11",
"12",
"13",
"14, 15",
"16, 17"
] | Recently, serum biomarker studies and imaging studies such as computerized tomography, magnetic resonance imaging, intima-media thickness, coronary angiography, optical coherence tomography, intravascular ultrasound (IVUS), and virtual histology IVUS (VH-IVUS) have been used to assess plaques. | true | true | true | true | true | 7,186 |
1 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 19,654,939 | pmid-11021830|pmid-11254922|pmid-16801474|pmid-17082488|pmid-17659199|pmid-17729343|pmid-17101043|pmid-17585387|pmid-16814652|pmid-16487837|pmid-16631508|pmid-16781367|pmid-12390948|pmid-15640160 | IVUS and VH-IVUS are the most commonly used tools in the evaluation of vulnerable plaques. | [
"5",
"6",
"7",
"8",
"9",
"10",
"11",
"12",
"13",
"14",
"15",
"16",
"17"
] | 90 | 41,668 | 0 | false | IVUS and VH-IVUS are the most commonly used tools in the evaluation of vulnerable plaques. | [] | IVUS and VH-IVUS are the most commonly used tools in the evaluation of vulnerable plaques. | true | true | true | true | true | 7,186 |
2 | INTRODUCTION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-15640160|pmid-17413036 | Nogo-B (reticulon 4 B) has been recently discovered as a member of the reticulon family of proteins. | [
"18"
] | 100 | 41,669 | 0 | false | Nogo-B (reticulon 4 B) has been recently discovered as a member of the reticulon family of proteins. | [] | Nogo-B (reticulon 4 B) has been recently discovered as a member of the reticulon family of proteins. | true | true | true | true | true | 7,187 |
2 | INTRODUCTION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-15640160|pmid-17413036 | The biological role of Nogo-B is not well understood. | [
"18"
] | 53 | 41,670 | 0 | false | The biological role of Nogo-B is not well understood. | [] | The biological role of Nogo-B is not well understood. | true | true | true | true | true | 7,187 |
2 | INTRODUCTION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-15640160|pmid-17413036 | Some animal data suggest that Nogo-B is associated with the promotion of endothelial migration and the inhibition of vascular smooth muscle cell migration, resulting in homeostasis and remodeling of vascular structures (18). | [
"18"
] | 224 | 41,671 | 1 | false | Some animal data suggest that Nogo-B is associated with the promotion of endothelial migration and the inhibition of vascular smooth muscle cell migration, resulting in homeostasis and remodeling of vascular structures. | [
"18"
] | Some animal data suggest that Nogo-B is associated with the promotion of endothelial migration and the inhibition of vascular smooth muscle cell migration, resulting in homeostasis and remodeling of vascular structures. | true | true | true | true | true | 7,187 |
2 | INTRODUCTION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-15640160|pmid-17413036 | However, there is limited human data, and the relationship between Nogo-B and the progression of fibroatheromas (FA) or vulnerable plaques is not well understood. | [
"18"
] | 162 | 41,672 | 0 | false | However, there is limited human data, and the relationship between Nogo-B and the progression of fibroatheromas (FA) or vulnerable plaques is not well understood. | [] | However, there is limited human data, and the relationship between Nogo-B and the progression of fibroatheromas (FA) or vulnerable plaques is not well understood. | true | true | true | true | true | 7,187 |
2 | INTRODUCTION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-15640160|pmid-17413036 | Thus, the purpose of this study was to evaluate the relationship between Nogo-B, and FA or plaque progression in human coronary arteries using VH-IVUS. | [
"18"
] | 151 | 41,673 | 0 | false | Thus, the purpose of this study was to evaluate the relationship between Nogo-B, and FA or plaque progression in human coronary arteries using VH-IVUS. | [] | Thus, the purpose of this study was to evaluate the relationship between Nogo-B, and FA or plaque progression in human coronary arteries using VH-IVUS. | true | true | true | true | true | 7,187 |
0 | DISCUSSION | 0 | null | null | 19,654,939 | pmid-16631505|pmid-17684150|pmid-17884367|pmid-11755373 | The present study demonstrated the inverse relation between Nogo-B expression and FA progression in autopsied coronary arteries. | null | 128 | 41,674 | 0 | false | null | null | The present study demonstrated the inverse relation between Nogo-B expression and FA progression in autopsied coronary arteries. | true | true | true | true | true | 7,188 |
0 | DISCUSSION | 0 | null | null | 19,654,939 | pmid-16631505|pmid-17684150|pmid-17884367|pmid-11755373 | This is the first human study assessing the correlation between Nogo-B and plaque composition analyzed by VH-IVUS. | null | 114 | 41,675 | 0 | false | null | null | This is the first human study assessing the correlation between Nogo-B and plaque composition analyzed by VH-IVUS. | true | true | true | true | true | 7,188 |
0 | DISCUSSION | 0 | null | null | 19,654,939 | pmid-16631505|pmid-17684150|pmid-17884367|pmid-11755373 | Our data revealed decreased expression of Nogo-B in advanced FA, including vulnerable TCFA plaques. | null | 99 | 41,676 | 0 | false | null | null | Our data revealed decreased expression of Nogo-B in advanced FA, including vulnerable TCFA plaques. | true | true | true | true | true | 7,188 |
1 | DISCUSSION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-11021830|pmid-11254922|pmid-16801474|pmid-17082488|pmid-17659199|pmid-17729343|pmid-17101043|pmid-17585387|pmid-16814652|pmid-16487837|pmid-16631508|pmid-16781367|pmid-12390948|pmid-15640160 | Nogo proteins are composed of three alternative splice forms: 1192-residue Nogo-A, 373-residue Nogo-B, and 199-residue Nogo-C. | [
"18"
] | 126 | 41,677 | 0 | false | Nogo proteins are composed of three alternative splice forms: 1192-residue Nogo-A, 373-residue Nogo-B, and 199-residue Nogo-C. | [] | Nogo proteins are composed of three alternative splice forms: 1192-residue Nogo-A, 373-residue Nogo-B, and 199-residue Nogo-C. | true | true | true | true | true | 7,189 |
1 | DISCUSSION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-11021830|pmid-11254922|pmid-16801474|pmid-17082488|pmid-17659199|pmid-17729343|pmid-17101043|pmid-17585387|pmid-16814652|pmid-16487837|pmid-16631508|pmid-16781367|pmid-12390948|pmid-15640160 | Despite their significantly different N-terminal lengths, they share a conserved C-terminal reticulon-homology domain consisting of two transmembrane fragments, a 66-residue extracellular loop (Nogo-66) and a 38-residue C-tail carrying an endoplasmic reticulum retention motif. | [
"18"
] | 277 | 41,678 | 0 | false | Despite their significantly different N-terminal lengths, they share a conserved C-terminal reticulon-homology domain consisting of two transmembrane fragments, a 66-residue extracellular loop (Nogo-66) and a 38-residue C-tail carrying an endoplasmic reticulum retention motif. | [] | Despite their significantly different N-terminal lengths, they share a conserved C-terminal reticulon-homology domain consisting of two transmembrane fragments, a 66-residue extracellular loop (Nogo-66) and a 38-residue C-tail carrying an endoplasmic reticulum retention motif. | true | true | true | true | true | 7,189 |
1 | DISCUSSION | 1 | 18 | [
"B18"
] | 19,654,939 | pmid-11021830|pmid-11254922|pmid-16801474|pmid-17082488|pmid-17659199|pmid-17729343|pmid-17101043|pmid-17585387|pmid-16814652|pmid-16487837|pmid-16631508|pmid-16781367|pmid-12390948|pmid-15640160 | Nogo-A has the largest N-terminus (1016 residues), while Nogo-B has an N-terminus almost identical to the first 200 residues of Nogo-A (18). | [
"18"
] | 140 | 41,679 | 1 | false | Nogo-A has the largest N-terminus (1016 residues), while Nogo-B has an N-terminus almost identical to the first 200 residues of Nogo-A. | [
"18"
] | Nogo-A has the largest N-terminus, while Nogo-B has an N-terminus almost identical to the first 200 residues of Nogo-A. | true | true | true | true | true | 7,189 |
2 | DISCUSSION | 1 | 21 | [
"B21"
] | 19,654,939 | pmid-15640160|pmid-17413036 | Rodriguez-Feo et al. | [
"21"
] | 20 | 41,680 | 0 | false | Rodriguez-Feo et al. | [] | Rodriguez-Feo et al. | true | true | true | true | true | 7,190 |
2 | DISCUSSION | 1 | 21 | [
"B21"
] | 19,654,939 | pmid-15640160|pmid-17413036 | (21) previously reported that Nogo-B levels in carotid plaques are inversely related with the presence of large lipid pools. | [
"21"
] | 124 | 41,681 | 1 | false | previously reported that Nogo-B levels in carotid plaques are inversely related with the presence of large lipid pools. | [
"21"
] | previously reported that Nogo-B levels in carotid plaques are inversely related with the presence of large lipid pools. | false | true | true | true | false | 7,190 |
2 | DISCUSSION | 1 | 21 | [
"B21"
] | 19,654,939 | pmid-15640160|pmid-17413036 | However, they classified roughly two groups based on a degree of carotid stenosis of 90% and a fat content of 40%. | [
"21"
] | 114 | 41,682 | 0 | false | However, they classified roughly two groups based on a degree of carotid stenosis of 90% and a fat content of 40%. | [] | However, they classified roughly two groups based on a degree of carotid stenosis of 90% and a fat content of 40%. | true | true | true | true | true | 7,190 |
2 | DISCUSSION | 1 | 21 | [
"B21"
] | 19,654,939 | pmid-15640160|pmid-17413036 | This is insufficient to analyze the relation between Nogo-B and plaque progression over time. | [
"21"
] | 93 | 41,683 | 0 | false | This is insufficient to analyze the relation between Nogo-B and plaque progression over time. | [] | This is insufficient to analyze the relation between Nogo-B and plaque progression over time. | true | true | true | true | true | 7,190 |
3 | DISCUSSION | 1 | 19 | [
"B19"
] | 19,654,939 | pmid-16037567 | We classified atherosclerotic plaques into 4 groups using VH-IVUS. | [
"19"
] | 66 | 41,684 | 0 | false | We classified atherosclerotic plaques into 4 groups using VH-IVUS. | [] | We classified atherosclerotic plaques into 4 groups using VH-IVUS. | true | true | true | true | true | 7,191 |
3 | DISCUSSION | 1 | 19 | [
"B19"
] | 19,654,939 | pmid-16037567 | Early FA with NC area <0.1 mm2 and late FA with NC area 0.1-1.0 mm2 were defined in the present study based on a previous investigation by Virmani et al. | [
"19"
] | 153 | 41,685 | 0 | false | Early FA with NC area <0.1 mm2 and late FA with NC area 0.1-1.0 mm2 were defined in the present study based on a previous investigation by Virmani et al. | [] | Early FA with NC area <0.1 mm2 and late FA with NC area 0.1-1.0 mm2 were defined in the present study based on a previous investigation by Virmani et al. | true | true | true | true | true | 7,191 |
3 | DISCUSSION | 1 | 19 | [
"B19"
] | 19,654,939 | pmid-16037567 | They performed morphometric plaque analysis and suggested four groups based on NC: pathologic intimal thickening without NC, early core FA with NC area 0.06±0.02 mm2, late core FA with NC area 0.84±0.08 mm2, and thin-cap atheroma. | [
"19"
] | 230 | 41,686 | 0 | false | They performed morphometric plaque analysis and suggested four groups based on NC: pathologic intimal thickening without NC, early core FA with NC area 0.06±0.02 mm2, late core FA with NC area 0.84±0.08 mm2, and thin-cap atheroma. | [] | They performed morphometric plaque analysis and suggested four groups based on NC: pathologic intimal thickening without NC, early core FA with NC area 0.06±0.02 mm2, late core FA with NC area 0.84±0.08 mm2, and thin-cap atheroma. | true | true | true | true | true | 7,191 |
4 | DISCUSSION | 1 | 22 | [
"B22",
"B23"
] | 19,654,939 | pmid-17502324|pmid-17138936 | TkCFA and TCFA are widely used VH-IVUS plaque classifications since the pathologic confirmation based on these classifications is very high, as the predictive accuracy is approximately 93.4% for fibrous, 94.6% for fibrofatty tissue, 95.1% for NC, and 96.8% for dense calcium (22). | [
"22",
"23"
] | 280 | 41,687 | 1 | false | TkCFA and TCFA are widely used VH-IVUS plaque classifications since the pathologic confirmation based on these classifications is very high, as the predictive accuracy is approximately 93.4% for fibrous, 94.6% for fibrofatty tissue, 95.1% for NC, and 96.8% for dense calcium. | [
"22"
] | TkCFA and TCFA are widely used VH-IVUS plaque classifications since the pathologic confirmation based on these classifications is very high, as the predictive accuracy is approximately 93.4% for fibrous, 94.6% for fibrofatty tissue, 95.1% for NC, and 96.8% for dense calcium. | true | true | true | true | true | 7,192 |
4 | DISCUSSION | 1 | 22 | [
"B22",
"B23"
] | 19,654,939 | pmid-17502324|pmid-17138936 | However, validation of VH-IVUS has a controversy yet. | [
"22",
"23"
] | 53 | 41,688 | 0 | false | However, validation of VH-IVUS has a controversy yet. | [] | However, validation of VH-IVUS has a controversy yet. | true | true | true | true | true | 7,192 |
4 | DISCUSSION | 1 | 22 | [
"B22",
"B23"
] | 19,654,939 | pmid-17502324|pmid-17138936 | An animal study by Granada et al. | [
"22",
"23"
] | 33 | 41,689 | 0 | false | An animal study by Granada et al. | [] | An animal study by Granada et al. | true | true | true | true | true | 7,192 |
4 | DISCUSSION | 1 | 23 | [
"B22",
"B23"
] | 19,654,939 | pmid-17502324|pmid-17138936 | demonstrated that the sensitivity of IVUS-VH for the detection of fibrous, fibrofatty, and necrotic core tissue was 76.1%, 46%, and 41.1% respectively (23). | [
"22",
"23"
] | 156 | 41,690 | 1 | false | demonstrated that the sensitivity of IVUS-VH for the detection of fibrous, fibrofatty, and necrotic core tissue was 76.1%, 46%, and 41.1% respectively. | [
"23"
] | demonstrated that the sensitivity of IVUS-VH for the detection of fibrous, fibrofatty, and necrotic core tissue was 76.1%, 46%, and 41.1% respectively. | false | true | true | true | false | 7,192 |
4 | DISCUSSION | 1 | 22 | [
"B22",
"B23"
] | 19,654,939 | pmid-17502324|pmid-17138936 | In the present study, the correlation of NC and coincidence of FA classification between VH-IVUS and pathology were 71%, and 94% respectively. | [
"22",
"23"
] | 142 | 41,691 | 0 | false | In the present study, the correlation of NC and coincidence of FA classification between VH-IVUS and pathology were 71%, and 94% respectively. | [] | In the present study, the correlation of NC and coincidence of FA classification between VH-IVUS and pathology were 71%, and 94% respectively. | true | true | true | true | true | 7,192 |
4 | DISCUSSION | 1 | 22 | [
"B22",
"B23"
] | 19,654,939 | pmid-17502324|pmid-17138936 | The study for validation and accuracy of VH-IVUS will be needed more in future. | [
"22",
"23"
] | 79 | 41,692 | 0 | false | The study for validation and accuracy of VH-IVUS will be needed more in future. | [] | The study for validation and accuracy of VH-IVUS will be needed more in future. | true | true | true | true | true | 7,192 |
5 | DISCUSSION | 1 | 24 | [
"B24",
"B1",
"B25"
] | 19,654,939 | pmid-9887164|pmid-16631505|pmid-16387286 | Atherosclerotic plaques are caused by abnormal cellular proliferation and migration, lipid deposition, and extracellular matrix accumulation (24). | [
"24",
"1",
"25"
] | 146 | 41,693 | 1 | false | Atherosclerotic plaques are caused by abnormal cellular proliferation and migration, lipid deposition, and extracellular matrix accumulation. | [
"24"
] | Atherosclerotic plaques are caused by abnormal cellular proliferation and migration, lipid deposition, and extracellular matrix accumulation. | true | true | true | true | true | 7,193 |
5 | DISCUSSION | 1 | 24 | [
"B24",
"B1",
"B25"
] | 19,654,939 | pmid-9887164|pmid-16631505|pmid-16387286 | Rupture-prone, vulnerable TCFAs are associated with a high inflammatory component and a large necrotic core accompanied by elevated proteolytic activity (1, 25). | [
"24",
"1",
"25"
] | 161 | 41,694 | 0 | false | Rupture-prone, vulnerable TCFAs are associated with a high inflammatory component and a large necrotic core accompanied by elevated proteolytic activity. | [
"1, 25"
] | Rupture-prone, vulnerable TCFAs are associated with a high inflammatory component and a large necrotic core accompanied by elevated proteolytic activity. | true | true | true | true | true | 7,193 |
6 | DISCUSSION | 1 | 26 | [
"B26",
"B28",
"B18"
] | 19,654,939 | pmid-12743005|pmid-18929245|pmid-15640160 | VH-IVUS revealed that core necrosis and calcification were more significant in advanced FA compared to early FA and late FA. | [
"26",
"28",
"18"
] | 124 | 41,695 | 0 | false | VH-IVUS revealed that core necrosis and calcification were more significant in advanced FA compared to early FA and late FA. | [] | VH-IVUS revealed that core necrosis and calcification were more significant in advanced FA compared to early FA and late FA. | true | true | true | true | true | 7,194 |
6 | DISCUSSION | 1 | 26 | [
"B26",
"B28",
"B18"
] | 19,654,939 | pmid-12743005|pmid-18929245|pmid-15640160 | There have been many studies looking at the positive correlation between coronary artery calcification and atherosclerosis progression or coronary artery disease (26-28). | [
"26",
"28",
"18"
] | 170 | 41,696 | 0 | false | There have been many studies looking at the positive correlation between coronary artery calcification and atherosclerosis progression or coronary artery disease. | [
"26-28"
] | There have been many studies looking at the positive correlation between coronary artery calcification and atherosclerosis progression or coronary artery disease. | true | true | true | true | true | 7,194 |
6 | DISCUSSION | 1 | 18 | [
"B26",
"B28",
"B18"
] | 19,654,939 | pmid-12743005|pmid-18929245|pmid-15640160 | Previous data have shown that the N-terminal regions of both Nogo-A and -B have a putative calcium binding site (18). | [
"26",
"28",
"18"
] | 117 | 41,697 | 1 | false | Previous data have shown that the N-terminal regions of both Nogo-A and -B have a putative calcium binding site. | [
"18"
] | Previous data have shown that the N-terminal regions of both Nogo-A and -B have a putative calcium binding site. | true | true | true | true | true | 7,194 |
6 | DISCUSSION | 1 | 26 | [
"B26",
"B28",
"B18"
] | 19,654,939 | pmid-12743005|pmid-18929245|pmid-15640160 | Therefore, we deduced that decreased expression of Nogo-B proteins could play a role in coronary artery calcification. | [
"26",
"28",
"18"
] | 118 | 41,698 | 0 | false | Therefore, we deduced that decreased expression of Nogo-B proteins could play a role in coronary artery calcification. | [] | Therefore, we deduced that decreased expression of Nogo-B proteins could play a role in coronary artery calcification. | true | true | true | true | true | 7,194 |
6 | DISCUSSION | 1 | 26 | [
"B26",
"B28",
"B18"
] | 19,654,939 | pmid-12743005|pmid-18929245|pmid-15640160 | However, our data showed that only three factors, such as plaque burden, core necrosis, and CD68 activity, were significantly negatively correlated with Nogo-B activity, while calcification, age, and fibrosis were not related with Nogo-B expression. | [
"26",
"28",
"18"
] | 249 | 41,699 | 0 | false | However, our data showed that only three factors, such as plaque burden, core necrosis, and CD68 activity, were significantly negatively correlated with Nogo-B activity, while calcification, age, and fibrosis were not related with Nogo-B expression. | [] | However, our data showed that only three factors, such as plaque burden, core necrosis, and CD68 activity, were significantly negatively correlated with Nogo-B activity, while calcification, age, and fibrosis were not related with Nogo-B expression. | true | true | true | true | true | 7,194 |
6 | DISCUSSION | 1 | 26 | [
"B26",
"B28",
"B18"
] | 19,654,939 | pmid-12743005|pmid-18929245|pmid-15640160 | These findings imply that the principal pathology of plaque progression and instability is increased core necrosis and inflammation, rather than increased calcium deposition. | [
"26",
"28",
"18"
] | 174 | 41,700 | 0 | false | These findings imply that the principal pathology of plaque progression and instability is increased core necrosis and inflammation, rather than increased calcium deposition. | [] | These findings imply that the principal pathology of plaque progression and instability is increased core necrosis and inflammation, rather than increased calcium deposition. | true | true | true | true | true | 7,194 |
6 | DISCUSSION | 1 | 26 | [
"B26",
"B28",
"B18"
] | 19,654,939 | pmid-12743005|pmid-18929245|pmid-15640160 | The role of calcium in atherosclerotic plaque progression is more complicated than we initially thought it to be. | [
"26",
"28",
"18"
] | 113 | 41,701 | 0 | false | The role of calcium in atherosclerotic plaque progression is more complicated than we initially thought it to be. | [] | The role of calcium in atherosclerotic plaque progression is more complicated than we initially thought it to be. | true | true | true | true | true | 7,194 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | We also found the expression pattern of Nogo-B to be interesting. | [
"29",
"30"
] | 65 | 41,702 | 0 | false | We also found the expression pattern of Nogo-B to be interesting. | [] | We also found the expression pattern of Nogo-B to be interesting. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Diffuse Nogo-B distribution was noted in early FA and in healthy arteries containing non-atherosclerotic plaques, while focal distribution was noted in diseased arteries containing atherosclerotic plaques, such as late FA and advanced FA. | [
"29",
"30"
] | 238 | 41,703 | 0 | false | Diffuse Nogo-B distribution was noted in early FA and in healthy arteries containing non-atherosclerotic plaques, while focal distribution was noted in diseased arteries containing atherosclerotic plaques, such as late FA and advanced FA. | [] | Diffuse Nogo-B distribution was noted in early FA and in healthy arteries containing non-atherosclerotic plaques, while focal distribution was noted in diseased arteries containing atherosclerotic plaques, such as late FA and advanced FA. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | The mechanism of this differing distribution pattern is unclear, but some mechanisms have been proposed. | [
"29",
"30"
] | 104 | 41,704 | 0 | false | The mechanism of this differing distribution pattern is unclear, but some mechanisms have been proposed. | [] | The mechanism of this differing distribution pattern is unclear, but some mechanisms have been proposed. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | One is endothelial shear stress (29). | [
"29",
"30"
] | 37 | 41,705 | 1 | false | One is endothelial shear stress. | [
"29"
] | One is endothelial shear stress. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Pressure, but not cellular stretch, has been associated with Nogo-B up-regulation in nonvascular cells. | [
"29",
"30"
] | 103 | 41,706 | 0 | false | Pressure, but not cellular stretch, has been associated with Nogo-B up-regulation in nonvascular cells. | [] | Pressure, but not cellular stretch, has been associated with Nogo-B up-regulation in nonvascular cells. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Low endothelial shear stress is a powerful local stimulus for atherogenesis, as well as formation and progression of early atherosclerotic plaques and differentiation of high-risk plaques. | [
"29",
"30"
] | 188 | 41,707 | 0 | false | Low endothelial shear stress is a powerful local stimulus for atherogenesis, as well as formation and progression of early atherosclerotic plaques and differentiation of high-risk plaques. | [] | Low endothelial shear stress is a powerful local stimulus for atherogenesis, as well as formation and progression of early atherosclerotic plaques and differentiation of high-risk plaques. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Thus, high Nogo-B expression presents in healthy arteries with continuous pulsatile and unidirectional endothelial shear stress. | [
"29",
"30"
] | 128 | 41,708 | 0 | false | Thus, high Nogo-B expression presents in healthy arteries with continuous pulsatile and unidirectional endothelial shear stress. | [] | Thus, high Nogo-B expression presents in healthy arteries with continuous pulsatile and unidirectional endothelial shear stress. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Disturbed laminar flow develops, and the pulsatile flow generates low and/or oscillatory endothelial shear stress, which induces low Nogo-B expression. | [
"29",
"30"
] | 151 | 41,709 | 0 | false | Disturbed laminar flow develops, and the pulsatile flow generates low and/or oscillatory endothelial shear stress, which induces low Nogo-B expression. | [] | Disturbed laminar flow develops, and the pulsatile flow generates low and/or oscillatory endothelial shear stress, which induces low Nogo-B expression. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 30 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Another possible mechanism is a complicated local inflammation, which not fully established yet (30). | [
"29",
"30"
] | 101 | 41,710 | 1 | false | Another possible mechanism is a complicated local inflammation, which not fully established yet. | [
"30"
] | Another possible mechanism is a complicated local inflammation, which not fully established yet. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Nogo-B expression was significantly negatively correlated with CD68 activity, but not with MMP-9 activity in the present study. | [
"29",
"30"
] | 127 | 41,711 | 0 | false | Nogo-B expression was significantly negatively correlated with CD68 activity, but not with MMP-9 activity in the present study. | [] | Nogo-B expression was significantly negatively correlated with CD68 activity, but not with MMP-9 activity in the present study. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Despite the overall reduced Nogo-B levels in plaques, local accumulation of Nogo-B is noted in macrophage-rich areas. | [
"29",
"30"
] | 117 | 41,712 | 0 | false | Despite the overall reduced Nogo-B levels in plaques, local accumulation of Nogo-B is noted in macrophage-rich areas. | [] | Despite the overall reduced Nogo-B levels in plaques, local accumulation of Nogo-B is noted in macrophage-rich areas. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Nogo-B also seems to be concentrated in macrophages or foam cells. | [
"29",
"30"
] | 66 | 41,713 | 0 | false | Nogo-B also seems to be concentrated in macrophages or foam cells. | [] | Nogo-B also seems to be concentrated in macrophages or foam cells. | true | true | true | true | true | 7,195 |
7 | DISCUSSION | 1 | 29 | [
"B29",
"B30"
] | 19,654,939 | pmid-17599600|pmid-17207665 | Hence, new materials inhibiting local inflammation and preventing Nogo-B reduction (e.g., through a Nogo-B eluting stent) might be helpful in managing coronary artery disease in the future. | [
"29",
"30"
] | 189 | 41,714 | 0 | false | Hence, new materials inhibiting local inflammation and preventing Nogo-B reduction (e.g., through a Nogo-B eluting stent) might be helpful in managing coronary artery disease in the future. | [] | Hence, new materials inhibiting local inflammation and preventing Nogo-B reduction (e.g., through a Nogo-B eluting stent) might be helpful in managing coronary artery disease in the future. | true | true | true | true | true | 7,195 |
8 | DISCUSSION | 0 | null | null | 19,654,939 | null | There are several limitations to the present study. | null | 51 | 41,715 | 0 | false | null | null | There are several limitations to the present study. | true | true | true | true | true | 7,196 |
8 | DISCUSSION | 0 | null | null | 19,654,939 | null | We could not investigate circulating levels of Nogo-B. | null | 54 | 41,716 | 0 | false | null | null | We could not investigate circulating levels of Nogo-B. | true | true | true | true | true | 7,196 |
8 | DISCUSSION | 0 | null | null | 19,654,939 | null | Thus, we could not determine if it serves as a surrogate biomarker of human atherosclerosis. | null | 92 | 41,717 | 0 | false | null | null | Thus, we could not determine if it serves as a surrogate biomarker of human atherosclerosis. | true | true | true | true | true | 7,196 |
8 | DISCUSSION | 0 | null | null | 19,654,939 | null | Another limitation of our study is the relatively small sample size. | null | 68 | 41,718 | 0 | false | null | null | Another limitation of our study is the relatively small sample size. | true | true | true | true | true | 7,196 |
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