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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3 | INTRODUCTION | 1 | 27 | [
"B11 B12 B13 B14 B15 B16",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B19",
"B23",
"B24",
"B25",
"B26",
"B27"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | PML-NBs are subnuclear domains which critically depend on the presence of the PML tumor suppressor protein and exert a variety of biological functions ranging from control of apoptosis to hematopoietic differentiation and gene transcription (27). | [
"11–16",
"17",
"18",
"19",
"20",
"21",
"22",
"19",
"23",
"24",
"25",
"26",
"27"
] | 246 | 43,019 | 1 | false | PML-NBs are subnuclear domains which critically depend on the presence of the PML tumor suppressor protein and exert a variety of biological functions ranging from control of apoptosis to hematopoietic differentiation and gene transcription. | [
"27"
] | PML-NBs are subnuclear domains which critically depend on the presence of the PML tumor suppressor protein and exert a variety of biological functions ranging from control of apoptosis to hematopoietic differentiation and gene transcription. | true | true | true | true | true | 7,454 |
4 | INTRODUCTION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B32",
"B28",
"B33",
"B33"
] | 20,507,904 | pmid-16840782|pmid-15128824|pmid-17574024|pmid-19595715|pmid-19737522|pmid-16840782|pmid-17574021|pmid-17574021 | Among the kinases that phosphorylate serine 468 and 536 is IKKε (also called IKKi), a non-canonical IKK (28,29). | [
"28",
"29",
"30",
"31",
"32",
"28",
"33",
"33"
] | 112 | 43,020 | 0 | false | Among the kinases that phosphorylate serine 468 and 536 is IKKε (also called IKKi), a non-canonical IKK. | [
"28,29"
] | Among the kinases that phosphorylate serine 468 and 536 is IKKε (also called IKKi), a non-canonical IKK. | true | true | true | true | true | 7,455 |
4 | INTRODUCTION | 1 | 30 | [
"B28",
"B29",
"B30",
"B31",
"B32",
"B28",
"B33",
"B33"
] | 20,507,904 | pmid-16840782|pmid-15128824|pmid-17574024|pmid-19595715|pmid-19737522|pmid-16840782|pmid-17574021|pmid-17574021 | IKKε is also an important mediator of the interferon response, as it phosphorylates the transcription factors IRF3 and IRF7, which form a complex with NF-κB to establish a multi-protein enhanceosome mediating the production of type I interferons (30). | [
"28",
"29",
"30",
"31",
"32",
"28",
"33",
"33"
] | 251 | 43,021 | 1 | false | IKKε is also an important mediator of the interferon response, as it phosphorylates the transcription factors IRF3 and IRF7, which form a complex with NF-κB to establish a multi-protein enhanceosome mediating the production of type I interferons. | [
"30"
] | IKKε is also an important mediator of the interferon response, as it phosphorylates the transcription factors IRF3 and IRF7, which form a complex with NF-κB to establish a multi-protein enhanceosome mediating the production of type I interferons. | true | true | true | true | true | 7,455 |
4 | INTRODUCTION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B32",
"B28",
"B33",
"B33"
] | 20,507,904 | pmid-16840782|pmid-15128824|pmid-17574024|pmid-19595715|pmid-19737522|pmid-16840782|pmid-17574021|pmid-17574021 | Recent evidence showed several additional functions for IKKε. | [
"28",
"29",
"30",
"31",
"32",
"28",
"33",
"33"
] | 61 | 43,022 | 0 | false | Recent evidence showed several additional functions for IKKε. | [] | Recent evidence showed several additional functions for IKKε. | true | true | true | true | true | 7,455 |
4 | INTRODUCTION | 1 | 31 | [
"B28",
"B29",
"B30",
"B31",
"B32",
"B28",
"B33",
"B33"
] | 20,507,904 | pmid-16840782|pmid-15128824|pmid-17574024|pmid-19595715|pmid-19737522|pmid-16840782|pmid-17574021|pmid-17574021 | The kinase also participates in the clearance of the nuclear receptor corepressor (NCoR) from distinct promoters (31). | [
"28",
"29",
"30",
"31",
"32",
"28",
"33",
"33"
] | 118 | 43,023 | 1 | false | The kinase also participates in the clearance of the nuclear receptor corepressor (NCoR) from distinct promoters. | [
"31"
] | The kinase also participates in the clearance of the nuclear receptor corepressor (NCoR) from distinct promoters. | true | true | true | true | true | 7,455 |
4 | INTRODUCTION | 1 | 32 | [
"B28",
"B29",
"B30",
"B31",
"B32",
"B28",
"B33",
"B33"
] | 20,507,904 | pmid-16840782|pmid-15128824|pmid-17574024|pmid-19595715|pmid-19737522|pmid-16840782|pmid-17574021|pmid-17574021 | Mouse models also revealed the importance of IKKε for low-grade chronic inflammation as it occurs in obesity (32). | [
"28",
"29",
"30",
"31",
"32",
"28",
"33",
"33"
] | 114 | 43,024 | 1 | false | Mouse models also revealed the importance of IKKε for low-grade chronic inflammation as it occurs in obesity. | [
"32"
] | Mouse models also revealed the importance of IKKε for low-grade chronic inflammation as it occurs in obesity. | true | true | true | true | true | 7,455 |
4 | INTRODUCTION | 1 | 28 | [
"B28",
"B29",
"B30",
"B31",
"B32",
"B28",
"B33",
"B33"
] | 20,507,904 | pmid-16840782|pmid-15128824|pmid-17574024|pmid-19595715|pmid-19737522|pmid-16840782|pmid-17574021|pmid-17574021 | Integrative genomic approaches identified IKKε as a breast cancer oncogene amplified and overexpressed in >30% of breast tumors and derived cell lines (28,33). | [
"28",
"29",
"30",
"31",
"32",
"28",
"33",
"33"
] | 159 | 43,025 | 0 | false | Integrative genomic approaches identified IKKε as a breast cancer oncogene amplified and overexpressed in >30% of breast tumors and derived cell lines. | [
"28,33"
] | Integrative genomic approaches identified IKKε as a breast cancer oncogene amplified and overexpressed in >30% of breast tumors and derived cell lines. | true | true | true | true | true | 7,455 |
4 | INTRODUCTION | 1 | 33 | [
"B28",
"B29",
"B30",
"B31",
"B32",
"B28",
"B33",
"B33"
] | 20,507,904 | pmid-16840782|pmid-15128824|pmid-17574024|pmid-19595715|pmid-19737522|pmid-16840782|pmid-17574021|pmid-17574021 | Overexpression of IKKε is sufficient to transform cells, whereas siRNA-mediated knockdown of the kinase decreases the survival of breast cancer cells (33). | [
"28",
"29",
"30",
"31",
"32",
"28",
"33",
"33"
] | 155 | 43,026 | 1 | false | Overexpression of IKKε is sufficient to transform cells, whereas siRNA-mediated knockdown of the kinase decreases the survival of breast cancer cells. | [
"33"
] | Overexpression of IKKε is sufficient to transform cells, whereas siRNA-mediated knockdown of the kinase decreases the survival of breast cancer cells. | true | true | true | true | true | 7,455 |
5 | INTRODUCTION | 0 | null | null | 20,507,904 | null | Here we have investigated the physiological role of regulatory p65 phosphorylation by reconstitution experiments. | null | 113 | 43,027 | 0 | false | null | null | Here we have investigated the physiological role of regulatory p65 phosphorylation by reconstitution experiments. | true | true | true | true | true | 7,456 |
5 | INTRODUCTION | 0 | null | null | 20,507,904 | null | The impact of p65 phosphorylation on gene expression was highly gene specific and accordingly p65 phosphorylation at serine 468 and 536 occurred at distinct intracellular locations. | null | 181 | 43,028 | 0 | false | null | null | The impact of p65 phosphorylation on gene expression was highly gene specific and accordingly p65 phosphorylation at serine 468 and 536 occurred at distinct intracellular locations. | true | true | true | true | true | 7,456 |
5 | INTRODUCTION | 0 | null | null | 20,507,904 | null | TNF stimulation resulted in the inducible association of IKKε to p65 and the p65-dependent transport of the kinase to the nucleus and PML-NBs. | null | 142 | 43,029 | 0 | false | null | null | TNF stimulation resulted in the inducible association of IKKε to p65 and the p65-dependent transport of the kinase to the nucleus and PML-NBs. | true | true | true | true | true | 7,456 |
5 | INTRODUCTION | 0 | null | null | 20,507,904 | null | IKKε was required for the expression of specific genes and ChIP experiments revealed the recruitment of IKKε to the control regions of many inflammatory target genes, thus identifying a novel role for IKKε in the nucleus. | null | 221 | 43,030 | 0 | false | null | null | IKKε was required for the expression of specific genes and ChIP experiments revealed the recruitment of IKKε to the control regions of many inflammatory target genes, thus identifying a novel role for IKKε in the nucleus. | true | true | true | true | true | 7,456 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | This study suggests that the functional relevance of a phosphorylation site is also influenced by its intracellular distribution. | [
"29",
"9",
"10"
] | 129 | 43,031 | 0 | false | This study suggests that the functional relevance of a phosphorylation site is also influenced by its intracellular distribution. | [] | This study suggests that the functional relevance of a phosphorylation site is also influenced by its intracellular distribution. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | While the p65 protein is found in the entire nucleus except the nucleolus in TNF-stimulated cells, the phosphorylated p65 proteins accumulate in specific subcellular regions. | [
"29",
"9",
"10"
] | 174 | 43,032 | 0 | false | While the p65 protein is found in the entire nucleus except the nucleolus in TNF-stimulated cells, the phosphorylated p65 proteins accumulate in specific subcellular regions. | [] | While the p65 protein is found in the entire nucleus except the nucleolus in TNF-stimulated cells, the phosphorylated p65 proteins accumulate in specific subcellular regions. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | Immunofluorescence experiments showed a strong enrichment of serine 536 phosphorylated p65 in the area surrounding the nucleus. | [
"29",
"9",
"10"
] | 127 | 43,033 | 0 | false | Immunofluorescence experiments showed a strong enrichment of serine 536 phosphorylated p65 in the area surrounding the nucleus. | [] | Immunofluorescence experiments showed a strong enrichment of serine 536 phosphorylated p65 in the area surrounding the nucleus. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | This localization is compatible with published data suggesting a functional role of p65 serine 536 phosphorylation for controlling the kinetics of p65 nuclear import (29). | [
"29",
"9",
"10"
] | 171 | 43,034 | 1 | false | This localization is compatible with published data suggesting a functional role of p65 serine 536 phosphorylation for controlling the kinetics of p65 nuclear import. | [
"29"
] | This localization is compatible with published data suggesting a functional role of p65 serine 536 phosphorylation for controlling the kinetics of p65 nuclear import. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | In contrast, p65 serine 468 phosphorylation was predominantly nuclear and occurred in a speckled distribution which shows strong accumulation of serine 468 phosphorylated p65 in distinct nuclear regions. | [
"29",
"9",
"10"
] | 203 | 43,035 | 0 | false | In contrast, p65 serine 468 phosphorylation was predominantly nuclear and occurred in a speckled distribution which shows strong accumulation of serine 468 phosphorylated p65 in distinct nuclear regions. | [] | In contrast, p65 serine 468 phosphorylation was predominantly nuclear and occurred in a speckled distribution which shows strong accumulation of serine 468 phosphorylated p65 in distinct nuclear regions. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | As several groups of NF-κB target genes are not randomly distributed in the genome and are enriched in distinct chromosomal clusters (9,10), it will be relevant to investigate whether these genomic regions are selectively enriched with phosphorylated p65. | [
"29",
"9",
"10"
] | 255 | 43,036 | 0 | false | As several groups of NF-κB target genes are not randomly distributed in the genome and are enriched in distinct chromosomal clusters, it will be relevant to investigate whether these genomic regions are selectively enriched with phosphorylated p65. | [
"9,10"
] | As several groups of NF-κB target genes are not randomly distributed in the genome and are enriched in distinct chromosomal clusters, it will be relevant to investigate whether these genomic regions are selectively enriched with phosphorylated p65. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | Our data show that the effects of p65 phosphorylation depend on the individual target gene, an observation which is supported by the microscopical data which revealed focal points of p65 phosphorylation in the nucleus. | [
"29",
"9",
"10"
] | 218 | 43,037 | 0 | false | Our data show that the effects of p65 phosphorylation depend on the individual target gene, an observation which is supported by the microscopical data which revealed focal points of p65 phosphorylation in the nucleus. | [] | Our data show that the effects of p65 phosphorylation depend on the individual target gene, an observation which is supported by the microscopical data which revealed focal points of p65 phosphorylation in the nucleus. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | The accumulation of phosphorylated p65 in distinct regions raises the question for the molecular mechanisms underlying this inhomogeneous distribution. | [
"29",
"9",
"10"
] | 151 | 43,038 | 0 | false | The accumulation of phosphorylated p65 in distinct regions raises the question for the molecular mechanisms underlying this inhomogeneous distribution. | [] | The accumulation of phosphorylated p65 in distinct regions raises the question for the molecular mechanisms underlying this inhomogeneous distribution. | true | true | true | true | true | 7,457 |
0 | DISCUSSION | 1 | 29 | [
"B29",
"B9",
"B10"
] | 20,507,904 | pmid-19483709|pmid-19302050|pmid-16485027|pmid-18267068|pmid-17047224|pmid-15128824|pmid-17707233|pmid-14527995 | Systematic approaches such as ChIP to CHIP experiments will help to address these important questions in the future. | [
"29",
"9",
"10"
] | 116 | 43,039 | 0 | false | Systematic approaches such as ChIP to CHIP experiments will help to address these important questions in the future. | [] | Systematic approaches such as ChIP to CHIP experiments will help to address these important questions in the future. | true | true | true | true | true | 7,457 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | Within a given cell type, stimulation with distinct NF-κB activating agents stereotypically allows the generation of DNA-binding dimers, while target gene expression displays clear differences in respect to the regulated genes (4). | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 231 | 43,040 | 1 | false | Within a given cell type, stimulation with distinct NF-κB activating agents stereotypically allows the generation of DNA-binding dimers, while target gene expression displays clear differences in respect to the regulated genes. | [
"4"
] | Within a given cell type, stimulation with distinct NF-κB activating agents stereotypically allows the generation of DNA-binding dimers, while target gene expression displays clear differences in respect to the regulated genes. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | In addition, co-regulated genes often show stimulus-specific dynamic parameters of the transcriptional response (3,41). | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 119 | 43,041 | 0 | false | In addition, co-regulated genes often show stimulus-specific dynamic parameters of the transcriptional response. | [
"3,41"
] | In addition, co-regulated genes often show stimulus-specific dynamic parameters of the transcriptional response. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | Our data support the idea that these key parameters are controlled by mechanisms that include post-translational modification of the DNA-binding subunits. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 154 | 43,042 | 0 | false | Our data support the idea that these key parameters are controlled by mechanisms that include post-translational modification of the DNA-binding subunits. | [] | Our data support the idea that these key parameters are controlled by mechanisms that include post-translational modification of the DNA-binding subunits. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | This study shows that the impact of each individual phosphorylation site is highly gene specific and that reporter gene assays are therefore not adequate to investigate the functional consequences of NF-κB modifications. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 220 | 43,043 | 0 | false | This study shows that the impact of each individual phosphorylation site is highly gene specific and that reporter gene assays are therefore not adequate to investigate the functional consequences of NF-κB modifications. | [] | This study shows that the impact of each individual phosphorylation site is highly gene specific and that reporter gene assays are therefore not adequate to investigate the functional consequences of NF-κB modifications. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | Our findings are in line with studies that extensively investigated the functional consequences of p65 serine 276 phosphorylation on gene expression (22,46–48). | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 160 | 43,044 | 0 | false | Our findings are in line with studies that extensively investigated the functional consequences of p65 serine 276 phosphorylation on gene expression. | [
"22,46–48"
] | Our findings are in line with studies that extensively investigated the functional consequences of p65 serine 276 phosphorylation on gene expression. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | The functional outcome for target gene transcription is strictly dependent on the individual phosphorylation site. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 114 | 43,045 | 0 | false | The functional outcome for target gene transcription is strictly dependent on the individual phosphorylation site. | [] | The functional outcome for target gene transcription is strictly dependent on the individual phosphorylation site. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | For example, mutation of serine 276 impairs Icam-1 transcription (22,49), while this study shows that prevention of serine 468 or 536 phosphorylation stimulates Icam-1 expression. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 179 | 43,046 | 0 | false | For example, mutation of serine 276 impairs Icam-1 transcription, while this study shows that prevention of serine 468 or 536 phosphorylation stimulates Icam-1 expression. | [
"22,49"
] | For example, mutation of serine 276 impairs Icam-1 transcription, while this study shows that prevention of serine 468 or 536 phosphorylation stimulates Icam-1 expression. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 50 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | While the Cxcl2 gene is not affected by serine 468 or 536 phosphorylation, a recent study revealed that expression of this gene is up-regulated by a phosphomimetic p65 threonine 435 aspartic acid mutant (50). | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 208 | 43,047 | 1 | false | While the Cxcl2 gene is not affected by serine 468 or 536 phosphorylation, a recent study revealed that expression of this gene is up-regulated by a phosphomimetic p65 threonine 435 aspartic acid mutant. | [
"50"
] | While the Cxcl2 gene is not affected by serine 468 or 536 phosphorylation, a recent study revealed that expression of this gene is up-regulated by a phosphomimetic p65 threonine 435 aspartic acid mutant. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | These gene-specific effects are not confined to phosphorylation sites, but have also been reported for p65 modifications by acetylation or monomethylation (15,51). | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 163 | 43,048 | 0 | false | These gene-specific effects are not confined to phosphorylation sites, but have also been reported for p65 modifications by acetylation or monomethylation. | [
"15,51"
] | These gene-specific effects are not confined to phosphorylation sites, but have also been reported for p65 modifications by acetylation or monomethylation. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | All these results are fully consistent with the NF-κB barcode hypothesis. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 73 | 43,049 | 0 | false | All these results are fully consistent with the NF-κB barcode hypothesis. | [] | All these results are fully consistent with the NF-κB barcode hypothesis. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | According to this concept, post-translational modifications alone or in combination, generate distinct patterns that function to direct transcription in a target gene-specific fashion. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 184 | 43,050 | 0 | false | According to this concept, post-translational modifications alone or in combination, generate distinct patterns that function to direct transcription in a target gene-specific fashion. | [] | According to this concept, post-translational modifications alone or in combination, generate distinct patterns that function to direct transcription in a target gene-specific fashion. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | Therefore it will be an important future task to identify the NF-κB modification patterns at different genomic NF-κB binding sites. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 131 | 43,051 | 0 | false | Therefore it will be an important future task to identify the NF-κB modification patterns at different genomic NF-κB binding sites. | [] | Therefore it will be an important future task to identify the NF-κB modification patterns at different genomic NF-κB binding sites. | true | true | true | true | true | 7,458 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B3",
"B41",
"B22",
"B46 B47 B48",
"B22",
"B49",
"B50",
"B15",
"B51"
] | 20,507,904 | pmid-19859064|pmid-18267068|pmid-16485027|pmid-16934762|pmid-18408078|pmid-18025230|pmid-18362169|pmid-19038492|pmid-18408078|pmid-15516339|pmid-20001970|pmid-19864627|pmid-18263619 | These results may bear the seeds for a new generation of NF-κB inhibitors which do not preclude general NF-κB functions but rather interfere with distinct groups of target genes. | [
"4",
"3",
"41",
"22",
"46–48",
"22",
"49",
"50",
"15",
"51"
] | 178 | 43,052 | 0 | false | These results may bear the seeds for a new generation of NF-κB inhibitors which do not preclude general NF-κB functions but rather interfere with distinct groups of target genes. | [] | These results may bear the seeds for a new generation of NF-κB inhibitors which do not preclude general NF-κB functions but rather interfere with distinct groups of target genes. | true | true | true | true | true | 7,458 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | In unstimulated cells, most of the endogenous IKKε protein is found in the cytosol, while a minor fraction localizes to nuclear speckles which most probably correspond to PML-NBs. | [
"31",
"52–56",
"57",
"58",
"59"
] | 179 | 43,053 | 0 | false | In unstimulated cells, most of the endogenous IKKε protein is found in the cytosol, while a minor fraction localizes to nuclear speckles which most probably correspond to PML-NBs. | [] | In unstimulated cells, most of the endogenous IKKε protein is found in the cytosol, while a minor fraction localizes to nuclear speckles which most probably correspond to PML-NBs. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | This constitutively nuclear fraction of IKKε can be found at very low levels in the promoter regions of specific genes such as Saa3 or Vcam1. | [
"31",
"52–56",
"57",
"58",
"59"
] | 141 | 43,054 | 0 | false | This constitutively nuclear fraction of IKKε can be found at very low levels in the promoter regions of specific genes such as Saa3 or Vcam1. | [] | This constitutively nuclear fraction of IKKε can be found at very low levels in the promoter regions of specific genes such as Saa3 or Vcam1. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | The relevance of the kinase activity for basal nuclear IKKε localization was seen by the analysis of the kinase inactive IKKε variant which was completely excluded from the nucleus. | [
"31",
"52–56",
"57",
"58",
"59"
] | 181 | 43,055 | 0 | false | The relevance of the kinase activity for basal nuclear IKKε localization was seen by the analysis of the kinase inactive IKKε variant which was completely excluded from the nucleus. | [] | The relevance of the kinase activity for basal nuclear IKKε localization was seen by the analysis of the kinase inactive IKKε variant which was completely excluded from the nucleus. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | But the kinase function of IKKε is also important for the TNF-induced nuclear import of IKKε. | [
"31",
"52–56",
"57",
"58",
"59"
] | 93 | 43,056 | 0 | false | But the kinase function of IKKε is also important for the TNF-induced nuclear import of IKKε. | [] | But the kinase function of IKKε is also important for the TNF-induced nuclear import of IKKε. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | A sequence inspection of IKKε did not reveal any obvious sequences with the potential to mediate nuclear import or export, suggesting that IKKε reaches the nucleus upon binding to a binding partner by a piggyback mechanism. | [
"31",
"52–56",
"57",
"58",
"59"
] | 223 | 43,057 | 0 | false | A sequence inspection of IKKε did not reveal any obvious sequences with the potential to mediate nuclear import or export, suggesting that IKKε reaches the nucleus upon binding to a binding partner by a piggyback mechanism. | [] | A sequence inspection of IKKε did not reveal any obvious sequences with the potential to mediate nuclear import or export, suggesting that IKKε reaches the nucleus upon binding to a binding partner by a piggyback mechanism. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | Accordingly, TNF stimulation allowed the phosphorylation-dependent association of IKKε to p65 (see Figure 6B). | [
"31",
"52–56",
"57",
"58",
"59"
] | 110 | 43,058 | 0 | false | Accordingly, TNF stimulation allowed the phosphorylation-dependent association of IKKε to p65 (see Figure 6B). | [] | Accordingly, TNF stimulation allowed the phosphorylation-dependent association of IKKε to p65 (see Figure 6B). | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | The stimulus-induced interaction between IKKε and p65, and an absent interaction in unstimulated cells is also compatible with the leptomycin B experiments. | [
"31",
"52–56",
"57",
"58",
"59"
] | 156 | 43,059 | 0 | false | The stimulus-induced interaction between IKKε and p65, and an absent interaction in unstimulated cells is also compatible with the leptomycin B experiments. | [] | The stimulus-induced interaction between IKKε and p65, and an absent interaction in unstimulated cells is also compatible with the leptomycin B experiments. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | These revealed nuclear accumulation of p65 but cytosolic localization of IKKε after blockage of nuclear export and in the absence of a stimulatory signal. | [
"31",
"52–56",
"57",
"58",
"59"
] | 154 | 43,060 | 0 | false | These revealed nuclear accumulation of p65 but cytosolic localization of IKKε after blockage of nuclear export and in the absence of a stimulatory signal. | [] | These revealed nuclear accumulation of p65 but cytosolic localization of IKKε after blockage of nuclear export and in the absence of a stimulatory signal. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | The role of p65 for nuclear import of IKKε was suggested by a lacking nuclear translocation of the kinase in p65−/− cells, but also by the parallel kinetics of IKKε and p65 during TNF-induced nuclear import and export. | [
"31",
"52–56",
"57",
"58",
"59"
] | 218 | 43,061 | 0 | false | The role of p65 for nuclear import of IKKε was suggested by a lacking nuclear translocation of the kinase in p65−/− cells, but also by the parallel kinetics of IKKε and p65 during TNF-induced nuclear import and export. | [] | The role of p65 for nuclear import of IKKε was suggested by a lacking nuclear translocation of the kinase in p65−/− cells, but also by the parallel kinetics of IKKε and p65 during TNF-induced nuclear import and export. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | Accordingly, a recent study showed the necessity of p65 for the recruitment of IKKε to the Inos promoter (31). | [
"31",
"52–56",
"57",
"58",
"59"
] | 110 | 43,062 | 1 | false | Accordingly, a recent study showed the necessity of p65 for the recruitment of IKKε to the Inos promoter. | [
"31"
] | Accordingly, a recent study showed the necessity of p65 for the recruitment of IKKε to the Inos promoter. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 52–56 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | In addition to p65, IKKε also phosphorylates further transcription factors including c-Rel, c-Jun, IRF3 and IRF7 (52–56). | [
"31",
"52–56",
"57",
"58",
"59"
] | 121 | 43,063 | 1 | false | In addition to p65, IKKε also phosphorylates further transcription factors including c-Rel, c-Jun, IRF3 and IRF7. | [
"52–56"
] | In addition to p65, IKKε also phosphorylates further transcription factors including c-Rel, c-Jun, IRF3 and IRF7. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | It will therefore be interesting to reveal a possible contribution of these proteins for the regulated nuclear uptake of IKKε. | [
"31",
"52–56",
"57",
"58",
"59"
] | 126 | 43,064 | 0 | false | It will therefore be interesting to reveal a possible contribution of these proteins for the regulated nuclear uptake of IKKε. | [] | It will therefore be interesting to reveal a possible contribution of these proteins for the regulated nuclear uptake of IKKε. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 31 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | Within the nucleus, IKKε can be found in the nucleoplasm and also partially in PML-NBs. | [
"31",
"52–56",
"57",
"58",
"59"
] | 87 | 43,065 | 0 | false | Within the nucleus, IKKε can be found in the nucleoplasm and also partially in PML-NBs. | [] | Within the nucleus, IKKε can be found in the nucleoplasm and also partially in PML-NBs. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 57 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | The integrity of these subnuclear structures depends on a PML domain which allows non-covalent binding to SUMO (57). | [
"31",
"52–56",
"57",
"58",
"59"
] | 116 | 43,066 | 1 | false | The integrity of these subnuclear structures depends on a PML domain which allows non-covalent binding to SUMO. | [
"57"
] | The integrity of these subnuclear structures depends on a PML domain which allows non-covalent binding to SUMO. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 58 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | Intriguingly, the vast majority of constitutive or inducible PML-NB resident proteins can be modified by SUMOylation, thus allowing the formation of protein meshworks that are glued together upon interaction of SUMO and SUMO-binding domains (58). | [
"31",
"52–56",
"57",
"58",
"59"
] | 246 | 43,067 | 1 | false | Intriguingly, the vast majority of constitutive or inducible PML-NB resident proteins can be modified by SUMOylation, thus allowing the formation of protein meshworks that are glued together upon interaction of SUMO and SUMO-binding domains. | [
"58"
] | Intriguingly, the vast majority of constitutive or inducible PML-NB resident proteins can be modified by SUMOylation, thus allowing the formation of protein meshworks that are glued together upon interaction of SUMO and SUMO-binding domains. | true | true | true | true | true | 7,459 |
2 | DISCUSSION | 1 | 59 | [
"B31",
"B52 B53 B54 B55 B56",
"B57",
"B58",
"B59"
] | 20,507,904 | pmid-18927578|pmid-16485027|pmid-14532125|pmid-17707233|pmid-17707233|pmid-14527995|pmid-18927578|pmid-19595715|pmid-16888014|pmid-15879144|pmid-17332413|NA|pmid-12702806|pmid-17081985|pmid-17545995|pmid-20188669 | The reversible retention of IKKε in PML-NBs may thus be explained by the recently discovered SUMOylation of this kinase (59). | [
"31",
"52–56",
"57",
"58",
"59"
] | 125 | 43,068 | 1 | false | The reversible retention of IKKε in PML-NBs may thus be explained by the recently discovered SUMOylation of this kinase. | [
"59"
] | The reversible retention of IKKε in PML-NBs may thus be explained by the recently discovered SUMOylation of this kinase. | true | true | true | true | true | 7,459 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | This study shows that Saa3 activation is dependent on p65 phosphorylation and also sensitive to IKKε expression, thus fitting a model where IKKε-mediated p65 phosphorylation is relevant for gene activation. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 206 | 43,069 | 0 | false | This study shows that Saa3 activation is dependent on p65 phosphorylation and also sensitive to IKKε expression, thus fitting a model where IKKε-mediated p65 phosphorylation is relevant for gene activation. | [] | This study shows that Saa3 activation is dependent on p65 phosphorylation and also sensitive to IKKε expression, thus fitting a model where IKKε-mediated p65 phosphorylation is relevant for gene activation. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | On the contrary, while Vcam1 similarly requires IKKε for optimal activation, loss of phosphorylation sites actually results in greater induction. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 145 | 43,070 | 0 | false | On the contrary, while Vcam1 similarly requires IKKε for optimal activation, loss of phosphorylation sites actually results in greater induction. | [] | On the contrary, while Vcam1 similarly requires IKKε for optimal activation, loss of phosphorylation sites actually results in greater induction. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | This suggests that there are yet further targets of IKKε phosphorylation that are relevant at least for Vcam1 expression or more generally, for the effect of IKKε mediated activation, as schematically summarized in Figure 8D. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 225 | 43,071 | 0 | false | This suggests that there are yet further targets of IKKε phosphorylation that are relevant at least for Vcam1 expression or more generally, for the effect of IKKε mediated activation, as schematically summarized in Figure 8D. | [] | This suggests that there are yet further targets of IKKε phosphorylation that are relevant at least for Vcam1 expression or more generally, for the effect of IKKε mediated activation, as schematically summarized in Figure 8D. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | Accordingly, recent data show that inducible chromatin recruitment of IKKε allows the c-Jun-dependent clearance of the corepressor NCoR from target promoters (31). | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 163 | 43,072 | 1 | false | Accordingly, recent data show that inducible chromatin recruitment of IKKε allows the c-Jun-dependent clearance of the corepressor NCoR from target promoters. | [
"31"
] | Accordingly, recent data show that inducible chromatin recruitment of IKKε allows the c-Jun-dependent clearance of the corepressor NCoR from target promoters. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | This would also explain the occurrence of IKKε at loci which control the expression of IKKε-independent genes. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 110 | 43,073 | 0 | false | This would also explain the occurrence of IKKε at loci which control the expression of IKKε-independent genes. | [] | This would also explain the occurrence of IKKε at loci which control the expression of IKKε-independent genes. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | The recent years have mounted evidence that some cytosolic components of the NF-κB signaling cascade (including IKKα, p38, GSK3β, COMMD1, etc.) | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 143 | 43,074 | 0 | false | The recent years have mounted evidence that some cytosolic components of the NF-κB signaling cascade (including IKKα, p38, GSK3β, COMMD1, etc.) | [] | The recent years have mounted evidence that some cytosolic components of the NF-κB signaling cascade | true | true | false | true | false | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | can also be found at selected NF-κB target genes where they participate in modification of the DNA-binding subunits or chromatin (7,60). | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 136 | 43,075 | 0 | false | can also be found at selected NF-κB target genes where they participate in modification of the DNA-binding subunits or chromatin. | [
"7,60"
] | can also be found at selected NF-κB target genes where they participate in modification of the DNA-binding subunits or chromatin. | false | true | true | true | false | 7,460 |
3 | DISCUSSION | 1 | 63 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | The IKKε-related IKKα protein, for example, regulates gene expression upon phosphorylation of histone H3 at serine 10 (61,62), the corepressor SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) (63) and the acetyl transferase CBP (64). | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 256 | 43,076 | 1 | false | The IKKε-related IKKα protein, for example, regulates gene expression upon phosphorylation of histone H3 at serine 10, the corepressor SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) and the acetyl transferase CBP. | [
"61,62",
"63",
"64"
] | The IKKε-related IKKα protein, for example, regulates gene expression upon phosphorylation of histone H3 at serine 10, the corepressor SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) and the acetyl transferase CBP. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | Also IKKα was found to associate with chromatin at control regions for the cIAP-2, Il-8 or Maspin genes (63,65), but the general mechanisms employed by IKKs to allow chromatin association remain to be elaborated. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 212 | 43,077 | 0 | false | Also IKKα was found to associate with chromatin at control regions for the cIAP-2, Il-8 or Maspin genes, but the general mechanisms employed by IKKs to allow chromatin association remain to be elaborated. | [
"63,65"
] | Also IKKα was found to associate with chromatin at control regions for the cIAP-2, Il-8 or Maspin genes, but the general mechanisms employed by IKKs to allow chromatin association remain to be elaborated. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | Our Re-ChIP experiments suggest that chromatin association via binding to p65 might only be relevant for a subset of binding sites, as they occur at the Saa3 and Vcam1 promoters. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 178 | 43,078 | 0 | false | Our Re-ChIP experiments suggest that chromatin association via binding to p65 might only be relevant for a subset of binding sites, as they occur at the Saa3 and Vcam1 promoters. | [] | Our Re-ChIP experiments suggest that chromatin association via binding to p65 might only be relevant for a subset of binding sites, as they occur at the Saa3 and Vcam1 promoters. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | Consistently and as exemplified by the Saa3 promoter, phosphorylation-dependent binding of IKKε to p65 is required for chromatin recruitment of IKKε (see also Figure 6C). | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 170 | 43,079 | 0 | false | Consistently and as exemplified by the Saa3 promoter, phosphorylation-dependent binding of IKKε to p65 is required for chromatin recruitment of IKKε (see also Figure 6C). | [] | Consistently and as exemplified by the Saa3 promoter, phosphorylation-dependent binding of IKKε to p65 is required for chromatin recruitment of IKKε (see also Figure 6C). | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | A detailed understanding of the mechanisms underlying chromatin recruitment of IKKs will therefore require unbiased and systematic genome-wide approaches. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 154 | 43,080 | 0 | false | A detailed understanding of the mechanisms underlying chromatin recruitment of IKKs will therefore require unbiased and systematic genome-wide approaches. | [] | A detailed understanding of the mechanisms underlying chromatin recruitment of IKKs will therefore require unbiased and systematic genome-wide approaches. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | This study also revealed the relevance of PML for appropriate targeting of IKKε to the nucleus. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 95 | 43,081 | 0 | false | This study also revealed the relevance of PML for appropriate targeting of IKKε to the nucleus. | [] | This study also revealed the relevance of PML for appropriate targeting of IKKε to the nucleus. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | Accordingly, cells expressing the oncogenic and dominant negative PML-RARα fusion protein failed to display inducible nuclear localization of IKKε. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 147 | 43,082 | 0 | false | Accordingly, cells expressing the oncogenic and dominant negative PML-RARα fusion protein failed to display inducible nuclear localization of IKKε. | [] | Accordingly, cells expressing the oncogenic and dominant negative PML-RARα fusion protein failed to display inducible nuclear localization of IKKε. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | This defect is rather attributable to delayed nuclear import and not to enhanced nuclear export, as PML-RARα-dependent blockage of TNF-triggered IKKε translocation occurred even in the presence of leptomycin B (Supplementary Figure S4). | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 236 | 43,083 | 0 | false | This defect is rather attributable to delayed nuclear import and not to enhanced nuclear export, as PML-RARα-dependent blockage of TNF-triggered IKKε translocation occurred even in the presence of leptomycin B (Supplementary Figure S4). | [] | This defect is rather attributable to delayed nuclear import and not to enhanced nuclear export, as PML-RARα-dependent blockage of TNF-triggered IKKε translocation occurred even in the presence of leptomycin B (Supplementary Figure S4). | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 66 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | This finding might explain the recently revealed dysregulation of the IKKε target gene Vcam1 that occurs in acute promyelocytic leukemia cells (66). | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 148 | 43,084 | 1 | false | This finding might explain the recently revealed dysregulation of the IKKε target gene Vcam1 that occurs in acute promyelocytic leukemia cells. | [
"66"
] | This finding might explain the recently revealed dysregulation of the IKKε target gene Vcam1 that occurs in acute promyelocytic leukemia cells. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | Aberrant gene expression of further IKKε-controlled genes would not be unexpected in acute promyelocytic leukemia cells, thus adding another example for the interplay between two oncogenes. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 189 | 43,085 | 0 | false | Aberrant gene expression of further IKKε-controlled genes would not be unexpected in acute promyelocytic leukemia cells, thus adding another example for the interplay between two oncogenes. | [] | Aberrant gene expression of further IKKε-controlled genes would not be unexpected in acute promyelocytic leukemia cells, thus adding another example for the interplay between two oncogenes. | true | true | true | true | true | 7,460 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B7",
"B60",
"B61",
"B62",
"B63",
"B64",
"B63",
"B65",
"B66"
] | 20,507,904 | pmid-15226358|pmid-8710491|pmid-11533489|pmid-14690596|pmid-19864627|pmid-7925300|pmid-12419806|pmid-12456660|pmid-9660950|pmid-15457532|pmid-17431096|pmid-18408078|pmid-9660950|pmid-15489227|pmid-19339690|pmid-19270718|pmid-17468759|pmid-17928811|pmid-19595715|pmid-18927578|pmid-19648011|pmid-12789343|pmid-12789342|pm... | Given the role of IKKε intracellular localization revealed here, it will also be relevant to investigate whether cancer cells overexpressing IKKε also show changes in the intracellular localisation of this breast cancer oncogene. | [
"31",
"7",
"60",
"61",
"62",
"63",
"64",
"63",
"65",
"66"
] | 229 | 43,086 | 0 | false | Given the role of IKKε intracellular localization revealed here, it will also be relevant to investigate whether cancer cells overexpressing IKKε also show changes in the intracellular localisation of this breast cancer oncogene. | [] | Given the role of IKKε intracellular localization revealed here, it will also be relevant to investigate whether cancer cells overexpressing IKKε also show changes in the intracellular localisation of this breast cancer oncogene. | true | true | true | true | true | 7,460 |
0 | DISCUSSION | 1 | 30 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | Our current studies show that IL-23 is required for the in vivo pulmonary IL-17 and IL-17F response to K. pneumoniae infection. | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 127 | 43,087 | 0 | false | Our current studies show that IL-23 is required for the in vivo pulmonary IL-17 and IL-17F response to K. pneumoniae infection. | [] | Our current studies show that IL-23 is required for the in vivo pulmonary IL-17 and IL-17F response to K. pneumoniae infection. | true | true | true | true | true | 7,461 |
0 | DISCUSSION | 1 | 30 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | These results are novel in the light of previous work suggesting other cytokine signals, namely IL-15, are responsible for the pulmonary IL-17 response to lipopolysaccharide (30). | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 179 | 43,088 | 1 | false | These results are novel in the light of previous work suggesting other cytokine signals, namely IL-15, are responsible for the pulmonary IL-17 response to lipopolysaccharide. | [
"30"
] | These results are novel in the light of previous work suggesting other cytokine signals, namely IL-15, are responsible for the pulmonary IL-17 response to lipopolysaccharide. | true | true | true | true | true | 7,461 |
0 | DISCUSSION | 1 | 30 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | Although IL-15 appears to play a role in IL-17 induction in other models of inflammation (31–33), our current data demonstrate a strict requirement for IL-23 in pulmonary IL-17/17F induction in response to K. pneumoniae challenge. | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 230 | 43,089 | 0 | false | Although IL-15 appears to play a role in IL-17 induction in other models of inflammation, our current data demonstrate a strict requirement for IL-23 in pulmonary IL-17/17F induction in response to K. pneumoniae challenge. | [
"31–33"
] | Although IL-15 appears to play a role in IL-17 induction in other models of inflammation, our current data demonstrate a strict requirement for IL-23 in pulmonary IL-17/17F induction in response to K. pneumoniae challenge. | true | true | true | true | true | 7,461 |
0 | DISCUSSION | 1 | 30 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | Our current work also identifies two potential sources of IL-23 in the lung—AMs and mDCs—and suggests IL-23 functions very early in lung response to pathogen compared with IL-12. | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 178 | 43,090 | 0 | false | Our current work also identifies two potential sources of IL-23 in the lung—AMs and mDCs—and suggests IL-23 functions very early in lung response to pathogen compared with IL-12. | [] | Our current work also identifies two potential sources of IL-23 in the lung—AMs and mDCs—and suggests IL-23 functions very early in lung response to pathogen compared with IL-12. | true | true | true | true | true | 7,461 |
0 | DISCUSSION | 1 | 30 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | As early as 4 h after in vitro exposure to bacteria, media from AM culture stimulates splenocyte IL-17 production, indicating a rapid induction of bioactive IL-23 (unpublished data). | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 182 | 43,091 | 0 | false | As early as 4 h after in vitro exposure to bacteria, media from AM culture stimulates splenocyte IL-17 production, indicating a rapid induction of bioactive IL-23 (unpublished data). | [] | As early as 4 h after in vitro exposure to bacteria, media from AM culture stimulates splenocyte IL-17 production, indicating a rapid induction of bioactive IL-23 (unpublished data). | true | true | true | true | true | 7,461 |
0 | DISCUSSION | 1 | 30 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | In contrast, IL-12 remained undetectable in AM culture supernatants even 24 h after in vitro challenge, and these supernatants did not induce splenocyte IFN-γ expression. | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 170 | 43,092 | 0 | false | In contrast, IL-12 remained undetectable in AM culture supernatants even 24 h after in vitro challenge, and these supernatants did not induce splenocyte IFN-γ expression. | [] | In contrast, IL-12 remained undetectable in AM culture supernatants even 24 h after in vitro challenge, and these supernatants did not induce splenocyte IFN-γ expression. | true | true | true | true | true | 7,461 |
0 | DISCUSSION | 1 | 30 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | These findings are consistent with prior work showing that AMs produce little or no IL-12 p70 in response to isolated challenge with K. pneumoniae or LPS (5, 24). | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 162 | 43,093 | 0 | false | These findings are consistent with prior work showing that AMs produce little or no IL-12 p70 in response to isolated challenge with K. pneumoniae or LPS. | [
"5, 24"
] | These findings are consistent with prior work showing that AMs produce little or no IL-12 p70 in response to isolated challenge with K. pneumoniae or LPS. | true | true | true | true | true | 7,461 |
0 | DISCUSSION | 1 | 34 | [
"bib30",
"bib31",
"bib33",
"bib5",
"bib24",
"bib34"
] | 16,157,683 | pmid-12574382|pmid-15485625|pmid-10679127|pmid-9922218|pmid-15356157|pmid-15546388 | Hence, AM may be more important in initiating the early “ThIL-17” response to this pathogen rather than directing T cells into Th1 polarization (34). | [
"30",
"31",
"33",
"5",
"24",
"34"
] | 149 | 43,094 | 1 | false | Hence, AM may be more important in initiating the early “ThIL-17” response to this pathogen rather than directing T cells into Th1 polarization. | [
"34"
] | Hence, AM may be more important in initiating the early “ThIL-17” response to this pathogen rather than directing T cells into Th1 polarization. | true | true | true | true | true | 7,461 |
1 | DISCUSSION | 0 | null | null | 16,157,683 | null | In vivo, up-regulation of IL-23 p19 in BAL cells is seen as early as 2 h after K. pneumoniae infection. | null | 103 | 43,095 | 0 | false | null | null | In vivo, up-regulation of IL-23 p19 in BAL cells is seen as early as 2 h after K. pneumoniae infection. | true | true | true | true | true | 7,462 |
1 | DISCUSSION | 0 | null | null | 16,157,683 | null | Cells obtained by BAL at this time are still more than 95% AMs, implicating these cells as the likely source of early IL-23 expression in the alveolar compartment, because they express p40 mRNA even before infection. | null | 216 | 43,096 | 0 | false | null | null | Cells obtained by BAL at this time are still more than 95% AMs, implicating these cells as the likely source of early IL-23 expression in the alveolar compartment, because they express p40 mRNA even before infection. | true | true | true | true | true | 7,462 |
1 | DISCUSSION | 0 | null | null | 16,157,683 | null | Hence, induction of p19 transcription likely regulates the onset of IL-23 production in air spaces. | null | 99 | 43,097 | 0 | false | null | null | Hence, induction of p19 transcription likely regulates the onset of IL-23 production in air spaces. | true | true | true | true | true | 7,462 |
1 | DISCUSSION | 0 | null | null | 16,157,683 | null | The early increase in BAL cell p19 mRNA is followed by greater expression 16–24 h after infection, a pattern observed in both BALF cells and lung homogenate. | null | 157 | 43,098 | 0 | false | null | null | The early increase in BAL cell p19 mRNA is followed by greater expression 16–24 h after infection, a pattern observed in both BALF cells and lung homogenate. | true | true | true | true | true | 7,462 |
1 | DISCUSSION | 0 | null | null | 16,157,683 | null | Whether this finding is due to the alveolar recruitment of additional cell types expressing IL-23 p19 or increased AM gene expression is unknown. | null | 145 | 43,099 | 0 | false | null | null | Whether this finding is due to the alveolar recruitment of additional cell types expressing IL-23 p19 or increased AM gene expression is unknown. | true | true | true | true | true | 7,462 |
2 | DISCUSSION | 1 | 17 | [
"bib17",
"bib5",
"bib35"
] | 16,157,683 | pmid-12417590|pmid-9922218|NA | Interestingly, we observed greater splenocyte IL-17 induction from bacteria-pulsed IL-12 p35−/− AM conditioned media compared with WT AM. | [
"17",
"5",
"35"
] | 137 | 43,100 | 0 | false | Interestingly, we observed greater splenocyte IL-17 induction from bacteria-pulsed IL-12 p35−/− AM conditioned media compared with WT AM. | [] | Interestingly, we observed greater splenocyte IL-17 induction from bacteria-pulsed IL-12 p35−/− AM conditioned media compared with WT AM. | true | true | true | true | true | 7,463 |
2 | DISCUSSION | 1 | 17 | [
"bib17",
"bib5",
"bib35"
] | 16,157,683 | pmid-12417590|pmid-9922218|NA | A regulatory role for IL-12 in IL-23–mediated signaling has been previously demonstrated (17), because IL-12 and IL-23 share a common p40 subunit and both require IL-12Rβ1 binding to signal. | [
"17",
"5",
"35"
] | 190 | 43,101 | 1 | false | A regulatory role for IL-12 in IL-23–mediated signaling has been previously demonstrated, because IL-12 and IL-23 share a common p40 subunit and both require IL-12Rβ1 binding to signal. | [
"17"
] | A regulatory role for IL-12 in IL-23–mediated signaling has been previously demonstrated, because IL-12 and IL-23 share a common p40 subunit and both require IL-12Rβ1 binding to signal. | true | true | true | true | true | 7,463 |
2 | DISCUSSION | 1 | 17 | [
"bib17",
"bib5",
"bib35"
] | 16,157,683 | pmid-12417590|pmid-9922218|NA | However, we were unable to measure IL-12 p70 in bacteria-stimulated AM supernatants, regardless of genotype. | [
"17",
"5",
"35"
] | 108 | 43,102 | 0 | false | However, we were unable to measure IL-12 p70 in bacteria-stimulated AM supernatants, regardless of genotype. | [] | However, we were unable to measure IL-12 p70 in bacteria-stimulated AM supernatants, regardless of genotype. | true | true | true | true | true | 7,463 |
2 | DISCUSSION | 1 | 17 | [
"bib17",
"bib5",
"bib35"
] | 16,157,683 | pmid-12417590|pmid-9922218|NA | One hypothesis is that AM production of bioactive IL-23 is greater in p35−/− AMs, because more intracellular p40 is available to combine with p19. | [
"17",
"5",
"35"
] | 146 | 43,103 | 0 | false | One hypothesis is that AM production of bioactive IL-23 is greater in p35−/− AMs, because more intracellular p40 is available to combine with p19. | [] | One hypothesis is that AM production of bioactive IL-23 is greater in p35−/− AMs, because more intracellular p40 is available to combine with p19. | true | true | true | true | true | 7,463 |
2 | DISCUSSION | 1 | 5 | [
"bib17",
"bib5",
"bib35"
] | 16,157,683 | pmid-12417590|pmid-9922218|NA | In support of this is, it has been shown that the elaboration of IL-12 p70 in AMs is under posttranscriptional control, and a second stimulus (such as IFN-γ) (5) is required for AM release of IL-12 p70 heterodimer in response to LPS. | [
"17",
"5",
"35"
] | 233 | 43,104 | 1 | false | In support of this is, it has been shown that the elaboration of IL-12 p70 in AMs is under posttranscriptional control, and a second stimulus (such as IFN-γ) is required for AM release of IL-12 p70 heterodimer in response to LPS. | [
"5"
] | In support of this is, it has been shown that the elaboration of IL-12 p70 in AMs is under posttranscriptional control, and a second stimulus (such as IFN-γ) is required for AM release of IL-12 p70 heterodimer in response to LPS. | true | true | true | true | true | 7,463 |
2 | DISCUSSION | 1 | 17 | [
"bib17",
"bib5",
"bib35"
] | 16,157,683 | pmid-12417590|pmid-9922218|NA | Of note, higher IL-17 levels in IL-12 p35−/− mice was not observed in vivo. | [
"17",
"5",
"35"
] | 75 | 43,105 | 0 | false | Of note, higher IL-17 levels in IL-12 p35−/− mice was not observed in vivo. | [] | Of note, higher IL-17 levels in IL-12 p35−/− mice was not observed in vivo. | true | true | true | true | true | 7,463 |
2 | DISCUSSION | 1 | 35 | [
"bib17",
"bib5",
"bib35"
] | 16,157,683 | pmid-12417590|pmid-9922218|NA | However, deficient STAT1 signaling results in augmented IL-23 and IL-17 expression in the context of respiratory syncytial virus infection (35). | [
"17",
"5",
"35"
] | 144 | 43,106 | 1 | false | However, deficient STAT1 signaling results in augmented IL-23 and IL-17 expression in the context of respiratory syncytial virus infection. | [
"35"
] | However, deficient STAT1 signaling results in augmented IL-23 and IL-17 expression in the context of respiratory syncytial virus infection. | true | true | true | true | true | 7,463 |
3 | DISCUSSION | 1 | 23 | [
"bib23",
"bib28",
"bib36"
] | 16,157,683 | pmid-12707317|pmid-12515817|pmid-8217188 | Our prior work has shown that TLR4 signaling is required for early IL-23 p19 and IL-17 mRNA expression in the lung challenged with K. pneumoniae (23). | [
"23",
"28",
"36"
] | 150 | 43,107 | 1 | false | Our prior work has shown that TLR4 signaling is required for early IL-23 p19 and IL-17 mRNA expression in the lung challenged with K. pneumoniae. | [
"23"
] | Our prior work has shown that TLR4 signaling is required for early IL-23 p19 and IL-17 mRNA expression in the lung challenged with K. pneumoniae. | true | true | true | true | true | 7,464 |
3 | DISCUSSION | 1 | 28 | [
"bib23",
"bib28",
"bib36"
] | 16,157,683 | pmid-12707317|pmid-12515817|pmid-8217188 | The greater up-regulation in p19 mRNA seen in mDCs compared with pDCs also supports a TLR4-dependent mechanism for IL-23 expression in this model, because granulocyte macrophage CSF–treated, bone marrow–derived mDCs are reported to express greater amounts of TLR4 and are more responsive to LPS than Flt3 ligand-generate... | [
"23",
"28",
"36"
] | 332 | 43,108 | 1 | false | The greater up-regulation in p19 mRNA seen in mDCs compared with pDCs also supports a TLR4-dependent mechanism for IL-23 expression in this model, because granulocyte macrophage CSF–treated, bone marrow–derived mDCs are reported to express greater amounts of TLR4 and are more responsive to LPS than Flt3 ligand-generate... | [
"28"
] | The greater up-regulation in p19 mRNA seen in mDCs compared with pDCs also supports a TLR4-dependent mechanism for IL-23 expression in this model, because granulocyte macrophage CSF–treated, bone marrow–derived mDCs are reported to express greater amounts of TLR4 and are more responsive to LPS than Flt3 ligand-generate... | true | true | true | true | true | 7,464 |
3 | DISCUSSION | 1 | 36 | [
"bib23",
"bib28",
"bib36"
] | 16,157,683 | pmid-12707317|pmid-12515817|pmid-8217188 | Our data lead us to speculate that mDCs play an important role in the IL-17 recall response to bacterial challenge as mDCs readily migrate to draining lymph nodes upon antigen capture, a function not readily shared by AMs (36). | [
"23",
"28",
"36"
] | 227 | 43,109 | 1 | false | Our data lead us to speculate that mDCs play an important role in the IL-17 recall response to bacterial challenge as mDCs readily migrate to draining lymph nodes upon antigen capture, a function not readily shared by AMs. | [
"36"
] | Our data lead us to speculate that mDCs play an important role in the IL-17 recall response to bacterial challenge as mDCs readily migrate to draining lymph nodes upon antigen capture, a function not readily shared by AMs. | true | true | true | true | true | 7,464 |
3 | DISCUSSION | 1 | 23 | [
"bib23",
"bib28",
"bib36"
] | 16,157,683 | pmid-12707317|pmid-12515817|pmid-8217188 | The subsequent T cell expansion, IL-17 expression, and augmented neutrophil recruitment as a result of the IL-23/IL-17 axis may represent a novel “cross-talk” loop between innate and adaptive pulmonary immunity, which enables the infected lung to more rapidly contain infection. | [
"23",
"28",
"36"
] | 278 | 43,110 | 0 | false | The subsequent T cell expansion, IL-17 expression, and augmented neutrophil recruitment as a result of the IL-23/IL-17 axis may represent a novel “cross-talk” loop between innate and adaptive pulmonary immunity, which enables the infected lung to more rapidly contain infection. | [] | The subsequent T cell expansion, IL-17 expression, and augmented neutrophil recruitment as a result of the IL-23/IL-17 axis may represent a novel “cross-talk” loop between innate and adaptive pulmonary immunity, which enables the infected lung to more rapidly contain infection. | true | true | true | true | true | 7,464 |
4 | DISCUSSION | 1 | 37 | [
"bib37",
"bib38",
"bib17",
"bib39"
] | 16,157,683 | pmid-1673147|pmid-10722626|pmid-12417590|pmid-12023369 | Although IL-12 p35 was not required for the pulmonary IL-17 response to K. pneumoniae, it was requisite for IFN-γ expression in this infection. | [
"37",
"38",
"17",
"39"
] | 143 | 43,111 | 0 | false | Although IL-12 p35 was not required for the pulmonary IL-17 response to K. pneumoniae, it was requisite for IFN-γ expression in this infection. | [] | Although IL-12 p35 was not required for the pulmonary IL-17 response to K. pneumoniae, it was requisite for IFN-γ expression in this infection. | true | true | true | true | true | 7,465 |
4 | DISCUSSION | 1 | 37 | [
"bib37",
"bib38",
"bib17",
"bib39"
] | 16,157,683 | pmid-1673147|pmid-10722626|pmid-12417590|pmid-12023369 | This finding is consistent with the well-studied stimulatory effect of IL-12 on IFN-γ expression (37) as well as prior work that demonstrates the requirement of intact IL-12 for the pulmonary IFN-γ response to infection (38). | [
"37",
"38",
"17",
"39"
] | 225 | 43,112 | 1 | false | This finding is consistent with the well-studied stimulatory effect of IL-12 on IFN-γ expression as well as prior work that demonstrates the requirement of intact IL-12 for the pulmonary IFN-γ response to infection. | [
"37",
"38"
] | This finding is consistent with the well-studied stimulatory effect of IL-12 on IFN-γ expression as well as prior work that demonstrates the requirement of intact IL-12 for the pulmonary IFN-γ response to infection. | true | true | true | true | true | 7,465 |
4 | DISCUSSION | 1 | 17 | [
"bib37",
"bib38",
"bib17",
"bib39"
] | 16,157,683 | pmid-1673147|pmid-10722626|pmid-12417590|pmid-12023369 | The inability of IL-23 to induce pulmonary IFN-γ expression in the absence of IL-12 is consistent with previous work showing the failure of recombinant IL-23 to induce splenocyte IFN-γ expression, despite up-regulation of IL-17 by this cytokine (17). | [
"37",
"38",
"17",
"39"
] | 250 | 43,113 | 1 | false | The inability of IL-23 to induce pulmonary IFN-γ expression in the absence of IL-12 is consistent with previous work showing the failure of recombinant IL-23 to induce splenocyte IFN-γ expression, despite up-regulation of IL-17 by this cytokine. | [
"17"
] | The inability of IL-23 to induce pulmonary IFN-γ expression in the absence of IL-12 is consistent with previous work showing the failure of recombinant IL-23 to induce splenocyte IFN-γ expression, despite up-regulation of IL-17 by this cytokine. | true | true | true | true | true | 7,465 |
4 | DISCUSSION | 1 | 37 | [
"bib37",
"bib38",
"bib17",
"bib39"
] | 16,157,683 | pmid-1673147|pmid-10722626|pmid-12417590|pmid-12023369 | These observations are likely the result of differential receptor affinity and intracellular signaling events induced by IL-12 and IL-23. | [
"37",
"38",
"17",
"39"
] | 137 | 43,114 | 0 | false | These observations are likely the result of differential receptor affinity and intracellular signaling events induced by IL-12 and IL-23. | [] | These observations are likely the result of differential receptor affinity and intracellular signaling events induced by IL-12 and IL-23. | true | true | true | true | true | 7,465 |
4 | DISCUSSION | 1 | 37 | [
"bib37",
"bib38",
"bib17",
"bib39"
] | 16,157,683 | pmid-1673147|pmid-10722626|pmid-12417590|pmid-12023369 | IL-12 binding to the IL-12Rβ1/Rβ2 complex predominantly activates STAT4. | [
"37",
"38",
"17",
"39"
] | 72 | 43,115 | 0 | false | IL-12 binding to the IL-12Rβ1/Rβ2 complex predominantly activates STAT4. | [] | IL-12 binding to the IL-12Rβ1/Rβ2 complex predominantly activates STAT4. | true | true | true | true | true | 7,465 |
4 | DISCUSSION | 1 | 39 | [
"bib37",
"bib38",
"bib17",
"bib39"
] | 16,157,683 | pmid-1673147|pmid-10722626|pmid-12417590|pmid-12023369 | In contrast, IL-23 binds to the IL-23R/IL-12Rβ1 complex and induces STAT3, STAT1, and possibly STAT3/STAT4 heterodimer nuclear translocation, while only weakly activating STAT4 (39). | [
"37",
"38",
"17",
"39"
] | 182 | 43,116 | 1 | false | In contrast, IL-23 binds to the IL-23R/IL-12Rβ1 complex and induces STAT3, STAT1, and possibly STAT3/STAT4 heterodimer nuclear translocation, while only weakly activating STAT4. | [
"39"
] | In contrast, IL-23 binds to the IL-23R/IL-12Rβ1 complex and induces STAT3, STAT1, and possibly STAT3/STAT4 heterodimer nuclear translocation, while only weakly activating STAT4. | true | true | true | true | true | 7,465 |
5 | DISCUSSION | 0 | null | null | 16,157,683 | null | Our finding of decreased survival following pulmonary K. pneumoniae infection in both p35−/− and p40−/− mice is consistent with other reports of the importance of intact IL-12 signaling in this infection model. | null | 210 | 43,117 | 0 | false | null | null | Our finding of decreased survival following pulmonary K. pneumoniae infection in both p35−/− and p40−/− mice is consistent with other reports of the importance of intact IL-12 signaling in this infection model. | true | true | true | true | true | 7,466 |
5 | DISCUSSION | 0 | null | null | 16,157,683 | null | The early and universal mortality observed in the p40−/− group compared with other strains suggests roles for both IL-12 and IL-23 in host defense. | null | 147 | 43,118 | 0 | false | null | null | The early and universal mortality observed in the p40−/− group compared with other strains suggests roles for both IL-12 and IL-23 in host defense. | true | true | true | true | true | 7,466 |
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