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 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | In Saccharomyces cerevisiae, the phosphoinositol-3-kinase-like (PIK) kinase Mec1 occupies a central role in the DDR. | [
"1",
"2",
"3"
] | 116 | 43,419 | 0 | false | In Saccharomyces cerevisiae, the phosphoinositol-3-kinase-like (PIK) kinase Mec1 occupies a central role in the DDR. | [] | In Saccharomyces cerevisiae, the phosphoinositol-3-kinase-like (PIK) kinase Mec1 occupies a central role in the DDR. | true | true | true | true | true | 7,518 |
0 | INTRODUCTION | 1 | 2 | [
"B1",
"B2",
"B3"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | The other PIK-kinase, Tel1, plays a minor role in the DDR in wild-type cells (2). | [
"1",
"2",
"3"
] | 81 | 43,420 | 1 | false | The other PIK-kinase, Tel1, plays a minor role in the DDR in wild-type cells. | [
"2"
] | The other PIK-kinase, Tel1, plays a minor role in the DDR in wild-type cells. | true | true | true | true | true | 7,518 |
0 | INTRODUCTION | 1 | 3 | [
"B1",
"B2",
"B3"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | Unlike ATM in mammalian cells, where phosphorylation of residue serine 1981 is indicative of ATM activation (3), there is no direct assay to monitor activation of ATR or Mec1 kinase in vivo. | [
"1",
"2",
"3"
] | 190 | 43,421 | 1 | false | Unlike ATM in mammalian cells, where phosphorylation of residue serine 1981 is indicative of ATM activation, there is no direct assay to monitor activation of ATR or Mec1 kinase in vivo. | [
"3"
] | Unlike ATM in mammalian cells, where phosphorylation of residue serine 1981 is indicative of ATM activation, there is no direct assay to monitor activation of ATR or Mec1 kinase in vivo. | true | true | true | true | true | 7,518 |
1 | INTRODUCTION | 1 | 4 | [
"B4",
"B5",
"B6",
"B7",
"B6",
"B1"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | Mec1 is targeted to ssDNA covered by the ssDNA-binding protein RPA through its DNA-binding subunit Ddc2, an ortholog of ATRIP in mammalian cells (4). | [
"4",
"5",
"6",
"7",
"6",
"1"
] | 149 | 43,422 | 1 | false | Mec1 is targeted to ssDNA covered by the ssDNA-binding protein RPA through its DNA-binding subunit Ddc2, an ortholog of ATRIP in mammalian cells. | [
"4"
] | Mec1 is targeted to ssDNA covered by the ssDNA-binding protein RPA through its DNA-binding subunit Ddc2, an ortholog of ATRIP in mammalian cells. | true | true | true | true | true | 7,519 |
1 | INTRODUCTION | 1 | 4 | [
"B4",
"B5",
"B6",
"B7",
"B6",
"B1"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | ssDNA can accumulate as a result of replication fork stalling or during processing of DNA damage, such as the resection of a double-strand DNA break (DSB). | [
"4",
"5",
"6",
"7",
"6",
"1"
] | 155 | 43,423 | 0 | false | ssDNA can accumulate as a result of replication fork stalling or during processing of DNA damage, such as the resection of a double-strand DNA break (DSB). | [] | ssDNA can accumulate as a result of replication fork stalling or during processing of DNA damage, such as the resection of a double-strand DNA break (DSB). | false | true | true | true | false | 7,519 |
1 | INTRODUCTION | 1 | 4 | [
"B4",
"B5",
"B6",
"B7",
"B6",
"B1"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | DDR activation requires the colocalization of Mec1-Ddc2 and the 9-1-1 complex, a PCNA-like clamp composed of the Rad17, Mec3 and Ddc1 proteins in S. cerevisiae (5,6). | [
"4",
"5",
"6",
"7",
"6",
"1"
] | 166 | 43,424 | 0 | false | DDR activation requires the colocalization of Mec1-Ddc2 and the 9-1-1 complex, a PCNA-like clamp composed of the Rad17, Mec3 and Ddc1 proteins in S. cerevisiae. | [
"5,6"
] | DDR activation requires the colocalization of Mec1-Ddc2 and the 9-1-1 complex, a PCNA-like clamp composed of the Rad17, Mec3 and Ddc1 proteins in S. cerevisiae. | true | true | true | true | true | 7,519 |
1 | INTRODUCTION | 1 | 7 | [
"B4",
"B5",
"B6",
"B7",
"B6",
"B1"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | Biochemical reconstitution experiments showed that efficient Mec1 kinase activity requires the proper loading of the 9-1-1 complex by its clamp loader Rad24-RFC onto partial duplex DNA (7). | [
"4",
"5",
"6",
"7",
"6",
"1"
] | 189 | 43,425 | 1 | false | Biochemical reconstitution experiments showed that efficient Mec1 kinase activity requires the proper loading of the 9-1-1 complex by its clamp loader Rad24-RFC onto partial duplex DNA. | [
"7"
] | Biochemical reconstitution experiments showed that efficient Mec1 kinase activity requires the proper loading of the 9-1-1 complex by its clamp loader Rad24-RFC onto partial duplex DNA. | true | true | true | true | true | 7,519 |
1 | INTRODUCTION | 1 | 6 | [
"B4",
"B5",
"B6",
"B7",
"B6",
"B1"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | Both sensor complexes, Mec1–Ddc2 and 9-1-1, recognize the DNA damage independently of each other and their colocalization greatly enhances Mec1 activation (6). | [
"4",
"5",
"6",
"7",
"6",
"1"
] | 159 | 43,426 | 1 | false | Both sensor complexes, Mec1–Ddc2 and 9-1-1, recognize the DNA damage independently of each other and their colocalization greatly enhances Mec1 activation. | [
"6"
] | Both sensor complexes, Mec1–Ddc2 and 9-1-1, recognize the DNA damage independently of each other and their colocalization greatly enhances Mec1 activation. | true | true | true | true | true | 7,519 |
1 | INTRODUCTION | 1 | 1 | [
"B4",
"B5",
"B6",
"B7",
"B6",
"B1"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | The DNA damage signal is relayed through the damage-specific mediator Rad9 or the replication stress-specific mediator Mrc1 to the effector kinases, Chk1, Dun1 and Rad53 (1). | [
"4",
"5",
"6",
"7",
"6",
"1"
] | 174 | 43,427 | 1 | false | The DNA damage signal is relayed through the damage-specific mediator Rad9 or the replication stress-specific mediator Mrc1 to the effector kinases, Chk1, Dun1 and Rad53. | [
"1"
] | The DNA damage signal is relayed through the damage-specific mediator Rad9 or the replication stress-specific mediator Mrc1 to the effector kinases, Chk1, Dun1 and Rad53. | true | true | true | true | true | 7,519 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Activation of the Rad53 effector kinase is mediated by the Rad9 adaptor protein recruiting Rad53 as a substrate for Mec1 kinase (8). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 132 | 43,428 | 1 | false | Activation of the Rad53 effector kinase is mediated by the Rad9 adaptor protein recruiting Rad53 as a substrate for Mec1 kinase. | [
"8"
] | Activation of the Rad53 effector kinase is mediated by the Rad9 adaptor protein recruiting Rad53 as a substrate for Mec1 kinase. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 9 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Subsequent extensive autophosphorylation of Rad53 is indicative of activation and can be monitored through an electrophoretic mobility shift or an auto-kinase assay (9). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 169 | 43,429 | 1 | false | Subsequent extensive autophosphorylation of Rad53 is indicative of activation and can be monitored through an electrophoretic mobility shift or an auto-kinase assay. | [
"9"
] | Subsequent extensive autophosphorylation of Rad53 is indicative of activation and can be monitored through an electrophoretic mobility shift or an auto-kinase assay. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 9–16 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Rad53 activation has been taken as a general proxy for DDR activation in S. cerevisiae (9–16). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 94 | 43,430 | 1 | false | Rad53 activation has been taken as a general proxy for DDR activation in S. cerevisiae. | [
"9–16"
] | Rad53 activation has been taken as a general proxy for DDR activation in S. cerevisiae. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Genotoxic stress during different phases of the cell cycle poses distinct challenges. | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 85 | 43,431 | 0 | false | Genotoxic stress during different phases of the cell cycle poses distinct challenges. | [] | Genotoxic stress during different phases of the cell cycle poses distinct challenges. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 17 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | For example in G1, the absence of a sister chromatid impedes the use of recombinational repair, although in diploids the homolog can serve as a template (17). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 158 | 43,432 | 1 | false | For example in G1, the absence of a sister chromatid impedes the use of recombinational repair, although in diploids the homolog can serve as a template. | [
"17"
] | For example in G1, the absence of a sister chromatid impedes the use of recombinational repair, although in diploids the homolog can serve as a template. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 1 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | In S-phase, DNA repair requires coordination with DNA replication, and the DDR involves suppression of late firing origins (1). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 127 | 43,433 | 1 | false | In S-phase, DNA repair requires coordination with DNA replication, and the DDR involves suppression of late firing origins. | [
"1"
] | In S-phase, DNA repair requires coordination with DNA replication, and the DDR involves suppression of late firing origins. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Likewise in G2, mitosis and the onset of anaphase need to be coordinated with DNA repair. | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 89 | 43,434 | 0 | false | Likewise in G2, mitosis and the onset of anaphase need to be coordinated with DNA repair. | [] | Likewise in G2, mitosis and the onset of anaphase need to be coordinated with DNA repair. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | At the molecular level, this complexity is reflected in differences in the activation of Rad53 kinase in response to various forms of DNA damage in the G1 versus other phases of the cell cycle. | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 193 | 43,435 | 0 | false | At the molecular level, this complexity is reflected in differences in the activation of Rad53 kinase in response to various forms of DNA damage in the G1 versus other phases of the cell cycle. | [] | At the molecular level, this complexity is reflected in differences in the activation of Rad53 kinase in response to various forms of DNA damage in the G1 versus other phases of the cell cycle. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | In G1-arrested cells, Rad53 is not activated in response to oxidative DNA damage or a single DSB induced by HO-endonuclease (15,16,18). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 135 | 43,436 | 0 | false | In G1-arrested cells, Rad53 is not activated in response to oxidative DNA damage or a single DSB induced by HO-endonuclease. | [
"15,16,18"
] | In G1-arrested cells, Rad53 is not activated in response to oxidative DNA damage or a single DSB induced by HO-endonuclease. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 19 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Rad53 activation in G1 requires much higher concentrations of alkylation damage than in S or G2 (19). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 101 | 43,437 | 1 | false | Rad53 activation in G1 requires much higher concentrations of alkylation damage than in S or G2. | [
"19"
] | Rad53 activation in G1 requires much higher concentrations of alkylation damage than in S or G2. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 20 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | For UV, Rad53 activation requires damage processing by the nucleotide excision repair pathway specifically in G1, but not in S-phase (20). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 138 | 43,438 | 1 | false | For UV, Rad53 activation requires damage processing by the nucleotide excision repair pathway specifically in G1, but not in S-phase. | [
"20"
] | For UV, Rad53 activation requires damage processing by the nucleotide excision repair pathway specifically in G1, but not in S-phase. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | The damage is either repaired silently or the damage remains unrepaired until entry into S when the damage is processed. | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 120 | 43,439 | 0 | false | The damage is either repaired silently or the damage remains unrepaired until entry into S when the damage is processed. | [] | The damage is either repaired silently or the damage remains unrepaired until entry into S when the damage is processed. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Hence, activation of the DDR in G1-arrested budding yeast cells appears to be governed by different parameters than in other phases of the cell cycle. | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 150 | 43,440 | 0 | false | Hence, activation of the DDR in G1-arrested budding yeast cells appears to be governed by different parameters than in other phases of the cell cycle. | [] | Hence, activation of the DDR in G1-arrested budding yeast cells appears to be governed by different parameters than in other phases of the cell cycle. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 1 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | However, Rad53 activation does not measure the activation of the DDR at the sensor level but represents a stage in the signaling cascade, where already significant signal transduction and signal amplification has taken place (1). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 229 | 43,441 | 1 | false | However, Rad53 activation does not measure the activation of the DDR at the sensor level but represents a stage in the signaling cascade, where already significant signal transduction and signal amplification has taken place. | [
"1"
] | However, Rad53 activation does not measure the activation of the DDR at the sensor level but represents a stage in the signaling cascade, where already significant signal transduction and signal amplification has taken place. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 21 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | In mammalian cells, localized activation of the sensor kinase (ATM) is amplified to a pan-nuclear response in the activation of the effector kinases CHK1 and CHK2 (the mammalian homolog of yeast Rad53) during the DDR (21). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 222 | 43,442 | 1 | false | In mammalian cells, localized activation of the sensor kinase (ATM) is amplified to a pan-nuclear response in the activation of the effector kinases CHK1 and CHK2 (the mammalian homolog of yeast Rad53) during the DDR. | [
"21"
] | In mammalian cells, localized activation of the sensor kinase (ATM) is amplified to a pan-nuclear response in the activation of the effector kinases CHK1 and CHK2 (the mammalian homolog of yeast Rad53) during the DDR. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | The sensor kinases, ATM, ATR and their yeast paralogs have many phosphorylation substrates besides signaling components (22,23). | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 128 | 43,443 | 0 | false | The sensor kinases, ATM, ATR and their yeast paralogs have many phosphorylation substrates besides signaling components. | [
"22,23"
] | The sensor kinases, ATM, ATR and their yeast paralogs have many phosphorylation substrates besides signaling components. | true | true | true | true | true | 7,520 |
2 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B9 B10 B11 B12 B13 B14 B15 B16",
"B17",
"B1",
"B15",
"B16",
"B18",
"B19",
"B20",
"B1",
"B21",
"B22",
"B23"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | For lack of tools to monitor kinase activity in vivo, it is unclear whether the sensor kinases (primarily Mec1 in budding yeast) are activated under genotoxic stress conditions that fail to activate Rad53 kinase. | [
"8",
"9",
"9–16",
"17",
"1",
"15",
"16",
"18",
"19",
"20",
"1",
"21",
"22",
"23"
] | 212 | 43,444 | 0 | false | For lack of tools to monitor kinase activity in vivo, it is unclear whether the sensor kinases are activated under genotoxic stress conditions that fail to activate Rad53 kinase. | [
"primarily Mec1 in budding yeast"
] | For lack of tools to monitor kinase activity in vivo, it is unclear whether the sensor kinases are activated under genotoxic stress conditions that fail to activate Rad53 kinase. | true | true | true | true | true | 7,520 |
3 | INTRODUCTION | 1 | 24 | [
"B24",
"B25",
"B26",
"B27",
"B28",
"B27",
"B28"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Homologous recombination is a major pathway in the repair of DSBs, gaps, and interstrand crosslinks, as well as in the restart of stalled or broken replication forks (24). | [
"24",
"25",
"26",
"27",
"28",
"27",
"28"
] | 171 | 43,445 | 1 | false | Homologous recombination is a major pathway in the repair of DSBs, gaps, and interstrand crosslinks, as well as in the restart of stalled or broken replication forks. | [
"24"
] | Homologous recombination is a major pathway in the repair of DSBs, gaps, and interstrand crosslinks, as well as in the restart of stalled or broken replication forks. | true | true | true | true | true | 7,521 |
3 | INTRODUCTION | 1 | 24 | [
"B24",
"B25",
"B26",
"B27",
"B28",
"B27",
"B28"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Rad51 protein catalyzes the key reactions of homology search and DNA strand invasion. | [
"24",
"25",
"26",
"27",
"28",
"27",
"28"
] | 85 | 43,446 | 0 | false | Rad51 protein catalyzes the key reactions of homology search and DNA strand invasion. | [] | Rad51 protein catalyzes the key reactions of homology search and DNA strand invasion. | true | true | true | true | true | 7,521 |
3 | INTRODUCTION | 1 | 24 | [
"B24",
"B25",
"B26",
"B27",
"B28",
"B27",
"B28"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Rad55–Rad57 are two Rad51 paralogs in budding yeast with a specialized role in either formation or stabilization of the Rad51 filament (25,26). | [
"24",
"25",
"26",
"27",
"28",
"27",
"28"
] | 143 | 43,447 | 0 | false | Rad55–Rad57 are two Rad51 paralogs in budding yeast with a specialized role in either formation or stabilization of the Rad51 filament. | [
"25,26"
] | Rad55–Rad57 are two Rad51 paralogs in budding yeast with a specialized role in either formation or stabilization of the Rad51 filament. | true | true | true | true | true | 7,521 |
3 | INTRODUCTION | 1 | 24 | [
"B24",
"B25",
"B26",
"B27",
"B28",
"B27",
"B28"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Formation of an active Rad51 filament on ssDNA dedicates the substrate to recombinational repair, making Rad55–Rad57 an ideal regulatory target to modulate recombination. | [
"24",
"25",
"26",
"27",
"28",
"27",
"28"
] | 170 | 43,448 | 0 | false | Formation of an active Rad51 filament on ssDNA dedicates the substrate to recombinational repair, making Rad55–Rad57 an ideal regulatory target to modulate recombination. | [] | Formation of an active Rad51 filament on ssDNA dedicates the substrate to recombinational repair, making Rad55–Rad57 an ideal regulatory target to modulate recombination. | true | true | true | true | true | 7,521 |
3 | INTRODUCTION | 1 | 27 | [
"B24",
"B25",
"B26",
"B27",
"B28",
"B27",
"B28"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Indeed, Rad55 is a terminal target of the DDR after DNA damage or replication fork blockage (27). | [
"24",
"25",
"26",
"27",
"28",
"27",
"28"
] | 97 | 43,449 | 1 | false | Indeed, Rad55 is a terminal target of the DDR after DNA damage or replication fork blockage. | [
"27"
] | Indeed, Rad55 is a terminal target of the DDR after DNA damage or replication fork blockage. | true | true | true | true | true | 7,521 |
3 | INTRODUCTION | 1 | 28 | [
"B24",
"B25",
"B26",
"B27",
"B28",
"B27",
"B28"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Phosphorylation of an N-terminal cluster of serines (Rad55-S2,8,14) is important for full function of Rad55, and a non-phosphorylatable mutant (Rad55-S2,8,14A) leads to increased sensitivity to genotoxic stress (28). | [
"24",
"25",
"26",
"27",
"28",
"27",
"28"
] | 216 | 43,450 | 1 | false | Phosphorylation of an N-terminal cluster of serines (Rad55-S2,8,14) is important for full function of Rad55, and a non-phosphorylatable mutant (Rad55-S2,8,14A) leads to increased sensitivity to genotoxic stress. | [
"28"
] | Phosphorylation of an N-terminal cluster of serines is important for full function of Rad55, and a non-phosphorylatable mutant leads to increased sensitivity to genotoxic stress. | true | true | true | true | true | 7,521 |
3 | INTRODUCTION | 1 | 24 | [
"B24",
"B25",
"B26",
"B27",
"B28",
"B27",
"B28"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Rad55 phosphorylation after DNA damage causes an electrophoretic mobility shift, that is unchanged in the Rad55-S2,8,14A mutant protein, suggesting that a different phosphorylation site controls the mobility shift (27,28). | [
"24",
"25",
"26",
"27",
"28",
"27",
"28"
] | 222 | 43,451 | 0 | false | Rad55 phosphorylation after DNA damage causes an electrophoretic mobility shift, that is unchanged in the Rad55-S2,8,14A mutant protein, suggesting that a different phosphorylation site controls the mobility shift. | [
"27,28"
] | Rad55 phosphorylation after DNA damage causes an electrophoretic mobility shift, that is unchanged in the Rad55-S2,8,14A mutant protein, suggesting that a different phosphorylation site controls the mobility shift. | true | true | true | true | true | 7,521 |
4 | INTRODUCTION | 0 | null | null | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | In this study, we identify Rad55–S378 as the amino-acid residue that controls the phosphorylation event(s) leading to the electrophoretic mobility shift after DNA damage. | null | 170 | 43,452 | 0 | false | null | null | In this study, we identify Rad55–S378 as the amino-acid residue that controls the phosphorylation event(s) leading to the electrophoretic mobility shift after DNA damage. | true | true | true | true | true | 7,522 |
4 | INTRODUCTION | 0 | null | null | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | Rad55–S378 occurs in an SQ amino-acid sequence context, the preferred target site for PIK kinases, and a combination of in vivo and in vitro experiments identified S378 as a direct Mec1 site. | null | 191 | 43,453 | 0 | false | null | null | Rad55–S378 occurs in an SQ amino-acid sequence context, the preferred target site for PIK kinases, and a combination of in vivo and in vitro experiments identified S378 as a direct Mec1 site. | true | true | true | true | true | 7,522 |
4 | INTRODUCTION | 0 | null | null | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | Using the Rad55–S378 controlled mobility shift as a sentinel for Mec1 activation in vivo, our data show that Mec1 can be activated under conditions where Rad53 is not detectably activated. | null | 188 | 43,454 | 0 | false | null | null | Using the Rad55–S378 controlled mobility shift as a sentinel for Mec1 activation in vivo, our data show that Mec1 can be activated under conditions where Rad53 is not detectably activated. | true | true | true | true | true | 7,522 |
4 | INTRODUCTION | 0 | null | null | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | In G1-arrested cells expressing the HO-endonuclease, Mec1 but not Rad53 was activated, as demonstrated by phosphorylation of Rad55–S378, histone H2A (γ-H2A) and of RPA2. | null | 169 | 43,455 | 0 | false | null | null | In G1-arrested cells expressing the HO-endonuclease, Mec1 but not Rad53 was activated, as demonstrated by phosphorylation of Rad55–S378, histone H2A (γ-H2A) and of RPA2. | true | true | true | true | true | 7,522 |
4 | INTRODUCTION | 0 | null | null | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | This response depended on both Mec1–Ddc2 kinase complex and loading of the 9-1-1 clamp by Rad24-RFC. | null | 100 | 43,456 | 0 | false | null | null | This response depended on both Mec1–Ddc2 kinase complex and loading of the 9-1-1 clamp by Rad24-RFC. | true | true | true | true | true | 7,522 |
4 | INTRODUCTION | 0 | null | null | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | Our findings suggest the existence of a truncated DNA-damage-signaling pathway in G1-arrested cells that involves activation of Mec1 kinase but does not lead to activation of the full DDR involving activation of the effector kinases Dun1, Rad53, or Chk1. | null | 254 | 43,457 | 0 | false | null | null | Our findings suggest the existence of a truncated DNA-damage-signaling pathway in G1-arrested cells that involves activation of Mec1 kinase but does not lead to activation of the full DDR involving activation of the effector kinases Dun1, Rad53, or Chk1. | true | true | true | true | true | 7,522 |
0 | DISCUSSION | 1 | 50 | [
"B50"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | Using Rad55–S378 phosphorylation as a sentinel of Mec1 kinase activity in vivo we discovered a truncated DNA-damage-signaling pathway that is active in G1-arrested wild-type cells suffering limited DNA damage (a single DSB) and is constitutively activated in a number of mutants in genes involved in DNA metabolism (RAD5... | [
"50"
] | 342 | 43,458 | 0 | false | Using Rad55–S378 phosphorylation as a sentinel of Mec1 kinase activity in vivo we discovered a truncated DNA-damage-signaling pathway that is active in G1-arrested wild-type cells suffering limited DNA damage (a single DSB) and is constitutively activated in a number of mutants in genes involved in DNA metabolism. | [
"RAD50, MRC1, RAD9, RAD54"
] | Using Rad55–S378 phosphorylation as a sentinel of Mec1 kinase activity in vivo we discovered a truncated DNA-damage-signaling pathway that is active in G1-arrested wild-type cells suffering limited DNA damage (a single DSB) and is constitutively activated in a number of mutants in genes involved in DNA metabolism. | true | true | true | true | true | 7,523 |
0 | DISCUSSION | 1 | 50 | [
"B50"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | Activation of Mec1 kinase depended on both sensor components of the canonical DDR, the Mec1–Ddc2 complex and loading of the 9-1-1 complex by the Rad24-RFC. | [
"50"
] | 155 | 43,459 | 0 | false | Activation of Mec1 kinase depended on both sensor components of the canonical DDR, the Mec1–Ddc2 complex and loading of the 9-1-1 complex by the Rad24-RFC. | [] | Activation of Mec1 kinase depended on both sensor components of the canonical DDR, the Mec1–Ddc2 complex and loading of the 9-1-1 complex by the Rad24-RFC. | true | true | true | true | true | 7,523 |
0 | DISCUSSION | 1 | 50 | [
"B50"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | It appears that Mec1 kinase activation was restricted to the site of damage, targeting besides the DNA repair protein Rad55, histone H2A, and RPA2, which is bound to processed DSBs and where RPA provides the binding site for the Mec1–Ddc2 complex and the Rad24-RFC. | [
"50"
] | 265 | 43,460 | 0 | false | It appears that Mec1 kinase activation was restricted to the site of damage, targeting besides the DNA repair protein Rad55, histone H2A, and RPA2, which is bound to processed DSBs and where RPA provides the binding site for the Mec1–Ddc2 complex and the Rad24-RFC. | [] | It appears that Mec1 kinase activation was restricted to the site of damage, targeting besides the DNA repair protein Rad55, histone H2A, and RPA2, which is bound to processed DSBs and where RPA provides the binding site for the Mec1–Ddc2 complex and the Rad24-RFC. | true | true | true | true | true | 7,523 |
0 | DISCUSSION | 1 | 50 | [
"B50"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | However, the signaling cascade appears truncated after the sensor level, as there is no detectable activation of the effector kinases, most notably Rad53, and no evidence for phosphorylation of the adaptor proteins Rad9 and Mrc1. | [
"50"
] | 229 | 43,461 | 0 | false | However, the signaling cascade appears truncated after the sensor level, as there is no detectable activation of the effector kinases, most notably Rad53, and no evidence for phosphorylation of the adaptor proteins Rad9 and Mrc1. | [] | However, the signaling cascade appears truncated after the sensor level, as there is no detectable activation of the effector kinases, most notably Rad53, and no evidence for phosphorylation of the adaptor proteins Rad9 and Mrc1. | true | true | true | true | true | 7,523 |
0 | DISCUSSION | 1 | 50 | [
"B50"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | It is unlikely that the function of Rad53 kinase is replaced by the paralogous protein Mek1, which is known to function only during meiosis, where it substitutes for Rad53 in the meiotic checkpoint (50). | [
"50"
] | 203 | 43,462 | 1 | false | It is unlikely that the function of Rad53 kinase is replaced by the paralogous protein Mek1, which is known to function only during meiosis, where it substitutes for Rad53 in the meiotic checkpoint. | [
"50"
] | It is unlikely that the function of Rad53 kinase is replaced by the paralogous protein Mek1, which is known to function only during meiosis, where it substitutes for Rad53 in the meiotic checkpoint. | true | true | true | true | true | 7,523 |
0 | DISCUSSION | 1 | 50 | [
"B50"
] | 20,061,370 | pmid-18082599|pmid-11430828|pmid-12556884|pmid-14595109 | These data suggest that the DDR is not an ON/OFF switch, but capable of an intermediate level of activation (Supplementary Figure S2). | [
"50"
] | 134 | 43,463 | 0 | false | These data suggest that the DDR is not an ON/OFF switch, but capable of an intermediate level of activation (Supplementary Figure S2). | [] | These data suggest that the DDR is not an ON/OFF switch, but capable of an intermediate level of activation (Supplementary Figure S2). | true | true | true | true | true | 7,523 |
1 | DISCUSSION | 1 | 51 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | The bacterial SOS response fulfills a similar function as the eukaryotic DDR in enhancing survival and genomic stability. | [
"51",
"1",
"52",
"51"
] | 121 | 43,464 | 0 | false | The bacterial SOS response fulfills a similar function as the eukaryotic DDR in enhancing survival and genomic stability. | [] | The bacterial SOS response fulfills a similar function as the eukaryotic DDR in enhancing survival and genomic stability. | true | true | true | true | true | 7,524 |
1 | DISCUSSION | 1 | 51 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | The SOS response involves the regulation of the LexA transcriptional repressor that controls a suit of about 40 genes with functions in DNA repair (e.g. | [
"51",
"1",
"52",
"51"
] | 152 | 43,465 | 0 | false | The SOS response involves the regulation of the LexA transcriptional repressor that controls a suit of about 40 genes with functions in DNA repair (e.g. | [] | The SOS response involves the regulation of the LexA transcriptional repressor that controls a suit of about 40 genes with functions in DNA repair (e.g. | true | true | true | true | true | 7,524 |
1 | DISCUSSION | 1 | 51 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | recA, uvrA, uvrB, ruvA), DNA damage tolerance and mutagenesis (recA, umuC, umuD, DinB), replication restart (polB), cell division (sulA) and SOS autoregulation (lexA, recA, recX, dinI) (51). | [
"51",
"1",
"52",
"51"
] | 190 | 43,466 | 1 | false | recA, uvrA, uvrB, ruvA), DNA damage tolerance and mutagenesis (recA, umuC, umuD, DinB), replication restart (polB), cell division (sulA) and SOS autoregulation (lexA, recA, recX, dinI). | [
"51"
] | recA, uvrA, uvrB, ruvA), DNA damage tolerance and mutagenesis (recA, umuC, umuD, DinB), replication restart (polB), cell division (sulA) and SOS autoregulation (lexA, recA, recX, dinI). | false | true | true | true | false | 7,524 |
1 | DISCUSSION | 1 | 1 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | The DDR in eukaryotes is a kinase-signaling network that controls similar effector pathways in a mechanistically different way (1). | [
"51",
"1",
"52",
"51"
] | 131 | 43,467 | 1 | false | The DDR in eukaryotes is a kinase-signaling network that controls similar effector pathways in a mechanistically different way. | [
"1"
] | The DDR in eukaryotes is a kinase-signaling network that controls similar effector pathways in a mechanistically different way. | true | true | true | true | true | 7,524 |
1 | DISCUSSION | 1 | 51 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | However, the biological functions of both pathways in ensuring survival and genomic stability are highly similar. | [
"51",
"1",
"52",
"51"
] | 113 | 43,468 | 0 | false | However, the biological functions of both pathways in ensuring survival and genomic stability are highly similar. | [] | However, the biological functions of both pathways in ensuring survival and genomic stability are highly similar. | true | true | true | true | true | 7,524 |
1 | DISCUSSION | 1 | 51 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | The SOS response has been a paradigm for a complex regulatory network. | [
"51",
"1",
"52",
"51"
] | 70 | 43,469 | 0 | false | The SOS response has been a paradigm for a complex regulatory network. | [] | The SOS response has been a paradigm for a complex regulatory network. | true | true | true | true | true | 7,524 |
1 | DISCUSSION | 1 | 52 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | The level of DNA damage determines whether cells induce the full or a partial transcriptional program by regulation of the LexA repressor level and through the different architectures of the LexA-regulated promoters (52). | [
"51",
"1",
"52",
"51"
] | 221 | 43,470 | 1 | false | The level of DNA damage determines whether cells induce the full or a partial transcriptional program by regulation of the LexA repressor level and through the different architectures of the LexA-regulated promoters. | [
"52"
] | The level of DNA damage determines whether cells induce the full or a partial transcriptional program by regulation of the LexA repressor level and through the different architectures of the LexA-regulated promoters. | true | true | true | true | true | 7,524 |
1 | DISCUSSION | 1 | 51 | [
"B51",
"B1",
"B52",
"B51"
] | 20,061,370 | pmid-12791985|pmid-18471973|pmid-11691833|pmid-17189191|pmid-11691833|pmid-18082599|pmid-11333217|pmid-18082599|pmid-2108251|pmid-11333217 | This leads to the different levels of the SOS response through a temporal pattern of transcriptional induction leading from early/low level responses (uvrA, uvrB, uvrD) to additional responses as the level of DNA damage increases (RecA accumulation, cell-cycle arrest through induction of sulA, and induction of umuDC-de... | [
"51",
"1",
"52",
"51"
] | 356 | 43,471 | 1 | false | This leads to the different levels of the SOS response through a temporal pattern of transcriptional induction leading from early/low level responses (uvrA, uvrB, uvrD) to additional responses as the level of DNA damage increases (RecA accumulation, cell-cycle arrest through induction of sulA, and induction of umuDC-de... | [
"51"
] | This leads to the different levels of the SOS response through a temporal pattern of transcriptional induction leading from early/low level responses (uvrA, uvrB, uvrD) to additional responses as the level of DNA damage increases (RecA accumulation, cell-cycle arrest through induction of sulA, and induction of umuDC-de... | true | true | true | true | true | 7,524 |
2 | DISCUSSION | 1 | 34 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | There is evidence for a threshold in activating the DDR (measured as activation of Rad53) in the G1 and S-phases of the cell cycle (34,53). | [
"34",
"53",
"35"
] | 139 | 43,472 | 0 | false | There is evidence for a threshold in activating the DDR in the G1 and S-phases of the cell cycle. | [
"measured as activation of Rad53",
"34,53"
] | There is evidence for a threshold in activating the DDR in the G1 and S-phases of the cell cycle. | true | true | true | true | true | 7,525 |
2 | DISCUSSION | 1 | 34 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Given the mechanisms of the functionally similar SOS response in bacteria it appears unlikely that the eukaryotic DDR functions solely as a threshold-triggered ON/OFF switch. | [
"34",
"53",
"35"
] | 174 | 43,473 | 0 | false | Given the mechanisms of the functionally similar SOS response in bacteria it appears unlikely that the eukaryotic DDR functions solely as a threshold-triggered ON/OFF switch. | [] | Given the mechanisms of the functionally similar SOS response in bacteria it appears unlikely that the eukaryotic DDR functions solely as a threshold-triggered ON/OFF switch. | true | true | true | true | true | 7,525 |
2 | DISCUSSION | 1 | 34 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | Data presented here and in Barlow et al. | [
"34",
"53",
"35"
] | 40 | 43,474 | 0 | false | Data presented here and in Barlow et al. | [] | Data presented here and in Barlow et al. | true | true | true | true | true | 7,525 |
2 | DISCUSSION | 1 | 35 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | (35) provide evidence for the induction of the DDR in G1-arrested wild-type cells that is different from the canonical-signaling response in that it does not detectably activate Rad53 kinase. | [
"34",
"53",
"35"
] | 191 | 43,475 | 1 | false | provide evidence for the induction of the DDR in G1-arrested wild-type cells that is different from the canonical-signaling response in that it does not detectably activate Rad53 kinase. | [
"35"
] | provide evidence for the induction of the DDR in G1-arrested wild-type cells that is different from the canonical-signaling response in that it does not detectably activate Rad53 kinase. | false | true | true | true | false | 7,525 |
2 | DISCUSSION | 1 | 34 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | What could be the physiological function of such a limited activation of the DDR in yeast? | [
"34",
"53",
"35"
] | 90 | 43,476 | 0 | false | What could be the physiological function of such a limited activation of the DDR in yeast? | [] | What could be the physiological function of such a limited activation of the DDR in yeast? | true | true | true | true | true | 7,525 |
2 | DISCUSSION | 1 | 34 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | A deliberate partial response preempts a full DDR with an undesirable cell-cycle delay in response to DNA damage that is easily addressed during the S/G2 phase. | [
"34",
"53",
"35"
] | 160 | 43,477 | 0 | false | A deliberate partial response preempts a full DDR with an undesirable cell-cycle delay in response to DNA damage that is easily addressed during the S/G2 phase. | [] | A deliberate partial response preempts a full DDR with an undesirable cell-cycle delay in response to DNA damage that is easily addressed during the S/G2 phase. | true | true | true | true | true | 7,525 |
2 | DISCUSSION | 1 | 34 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | The number of Mec1 targets that have been identified under these conditions is limited to Rad55, histone H2A and RPA2, and more work is needed to identify additional G1 targets to uncover further effector processes that might be regulated under these conditions. | [
"34",
"53",
"35"
] | 262 | 43,478 | 0 | false | The number of Mec1 targets that have been identified under these conditions is limited to Rad55, histone H2A and RPA2, and more work is needed to identify additional G1 targets to uncover further effector processes that might be regulated under these conditions. | [] | The number of Mec1 targets that have been identified under these conditions is limited to Rad55, histone H2A and RPA2, and more work is needed to identify additional G1 targets to uncover further effector processes that might be regulated under these conditions. | true | true | true | true | true | 7,525 |
2 | DISCUSSION | 1 | 34 | [
"B34",
"B53",
"B35"
] | 20,061,370 | pmid-12049741|pmid-10562568|pmid-10562568|pmid-8600024|pmid-8553072|pmid-9657725|pmid-12917350|pmid-16365046|pmid-11239458|pmid-15496928|pmid-347306|pmid-18082599|pmid-11239458|pmid-15496928|pmid-11387222|pmid-12769855|pmid-10449414|pmid-18082599|pmid-12598907|pmid-17563356|pmid-17525332|pmid-18511906|pmid-12502744|pmi... | We speculate that RPA2, histone H2A, Rad55 phosphorylation may affect DSB processing, repair pathway or target (homolog) choice, or DNA replication. | [
"34",
"53",
"35"
] | 148 | 43,479 | 0 | false | We speculate that RPA2, histone H2A, Rad55 phosphorylation may affect DSB processing, repair pathway or target (homolog) choice, or DNA replication. | [] | We speculate that RPA2, histone H2A, Rad55 phosphorylation may affect DSB processing, repair pathway or target (homolog) choice, or DNA replication. | true | true | true | true | true | 7,525 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | What are the mechanisms that control the transition from the limited activation of the DDR in G1-arrested cells after a single DSB to a full response upon S-phase entry? | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 169 | 43,480 | 0 | false | What are the mechanisms that control the transition from the limited activation of the DDR in G1-arrested cells after a single DSB to a full response upon S-phase entry? | [] | What are the mechanisms that control the transition from the limited activation of the DDR in G1-arrested cells after a single DSB to a full response upon S-phase entry? | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | DSB processing is significantly more efficient in S/G2 cells than in G1-arrested cells and controlled by CDK phosphorylation of Sae2 (16,54). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 141 | 43,481 | 0 | false | DSB processing is significantly more efficient in S/G2 cells than in G1-arrested cells and controlled by CDK phosphorylation of Sae2. | [
"16,54"
] | DSB processing is significantly more efficient in S/G2 cells than in G1-arrested cells and controlled by CDK phosphorylation of Sae2. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | The accumulation of ssDNA leads to extensive RPA–ssDNA complexes that recruit more Mec1–Ddc2 kinase molecules and possibly 9-1-1 clamps (Supplementary Figure S2). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 162 | 43,482 | 0 | false | The accumulation of ssDNA leads to extensive RPA–ssDNA complexes that recruit more Mec1–Ddc2 kinase molecules and possibly 9-1-1 clamps (Supplementary Figure S2). | [] | The accumulation of ssDNA leads to extensive RPA–ssDNA complexes that recruit more Mec1–Ddc2 kinase molecules and possibly 9-1-1 clamps (Supplementary Figure S2). | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 34 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | This likely explains the threshold identified in G1 cells, where one, two, or three DSBs did not trigger Rad53 phosphorylation, but the addition of a fourth DSB caused Rad53 activation (34). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 190 | 43,483 | 1 | false | This likely explains the threshold identified in G1 cells, where one, two, or three DSBs did not trigger Rad53 phosphorylation, but the addition of a fourth DSB caused Rad53 activation. | [
"34"
] | This likely explains the threshold identified in G1 cells, where one, two, or three DSBs did not trigger Rad53 phosphorylation, but the addition of a fourth DSB caused Rad53 activation. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Physical assays detect limited DSB processing in G1-arrested cells (34,55). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 75 | 43,484 | 0 | false | Physical assays detect limited DSB processing in G1-arrested cells. | [
"34,55"
] | Physical assays detect limited DSB processing in G1-arrested cells. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 35 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | A proportion of such cells also contained RPA1 foci, another indication of DSB processing (35). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 95 | 43,485 | 1 | false | A proportion of such cells also contained RPA1 foci, another indication of DSB processing. | [
"35"
] | A proportion of such cells also contained RPA1 foci, another indication of DSB processing. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Our observation that RPA2 is phosphorylated under these conditions is consistent with Mec1 being active at a processed DSB. | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 123 | 43,486 | 0 | false | Our observation that RPA2 is phosphorylated under these conditions is consistent with Mec1 being active at a processed DSB. | [] | Our observation that RPA2 is phosphorylated under these conditions is consistent with Mec1 being active at a processed DSB. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | However, this mechanism does not explain why in G1 cells with a single DSB Mec1 kinase signaling is not transmitted to the effector kinases. | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 140 | 43,487 | 0 | false | However, this mechanism does not explain why in G1 cells with a single DSB Mec1 kinase signaling is not transmitted to the effector kinases. | [] | However, this mechanism does not explain why in G1 cells with a single DSB Mec1 kinase signaling is not transmitted to the effector kinases. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | It is interesting to note that Ddc1 and Ddc2 are not phosphorylated under these conditions (Figure 4B). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 103 | 43,488 | 0 | false | It is interesting to note that Ddc1 and Ddc2 are not phosphorylated under these conditions (Figure 4B). | [] | It is interesting to note that Ddc1 and Ddc2 are not phosphorylated under these conditions (Figure 4B). | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Both proteins are direct targets of Mec1 and phosphorylated during a normal S-phase and after DNA damage induction in a Rad53-independent fashion (43,44,56). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 157 | 43,489 | 0 | false | Both proteins are direct targets of Mec1 and phosphorylated during a normal S-phase and after DNA damage induction in a Rad53-independent fashion. | [
"43,44,56"
] | Both proteins are direct targets of Mec1 and phosphorylated during a normal S-phase and after DNA damage induction in a Rad53-independent fashion. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | The critical difference between these studies and our work is that Ddc1 and Ddc2 phosphorylation were observed under conditions (S-phase + UV, G2+UV) that led to full induction of the signaling cascade including Rad53 activation (43,44), unlike the limited induction in G1 cells with a single DSB used here. | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 307 | 43,490 | 0 | false | The critical difference between these studies and our work is that Ddc1 and Ddc2 phosphorylation were observed under conditions (S-phase + UV, G2+UV) that led to full induction of the signaling cascade including Rad53 activation, unlike the limited induction in G1 cells with a single DSB used here. | [
"43,44"
] | The critical difference between these studies and our work is that Ddc1 and Ddc2 phosphorylation were observed under conditions (S-phase + UV, G2+UV) that led to full induction of the signaling cascade including Rad53 activation, unlike the limited induction in G1 cells with a single DSB used here. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Dpb11 is an essential replication protein that functions in the S-M checkpoint to activate Mec1 directly or in conjunction with the 911 clamp (57,58). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 150 | 43,491 | 0 | false | Dpb11 is an essential replication protein that functions in the S-M checkpoint to activate Mec1 directly or in conjunction with the 911 clamp. | [
"57,58"
] | Dpb11 is an essential replication protein that functions in the S-M checkpoint to activate Mec1 directly or in conjunction with the 911 clamp. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | Phosphorylation recruits Dpb11, a mechanism conserved in fission yeast (59,60). | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 79 | 43,492 | 0 | false | Phosphorylation recruits Dpb11, a mechanism conserved in fission yeast. | [
"59,60"
] | Phosphorylation recruits Dpb11, a mechanism conserved in fission yeast. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | The absence of Ddc1 phosphorylation in G1-arrested cells with a single DSB and the association of Dpb11 with the replication fork suggest that Dpb11 is not involved. | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 165 | 43,493 | 0 | false | The absence of Ddc1 phosphorylation in G1-arrested cells with a single DSB and the association of Dpb11 with the replication fork suggest that Dpb11 is not involved. | [] | The absence of Ddc1 phosphorylation in G1-arrested cells with a single DSB and the association of Dpb11 with the replication fork suggest that Dpb11 is not involved. | true | true | true | true | true | 7,526 |
3 | DISCUSSION | 1 | 16 | [
"B16",
"B54",
"B34",
"B34",
"B55",
"B35",
"B43",
"B44",
"B56",
"B43",
"B44",
"B57",
"B58",
"B59",
"B60"
] | 20,061,370 | pmid-18166982|pmid-15369670|pmid-9159392|pmid-10825202|pmid-16966380|pmid-10825202|pmid-16966380|pmid-15496928|NA|pmid-18511906|pmid-18511906|pmid-12453425|pmid-18406328|pmid-10950868|pmid-9670034|pmid-10559981|pmid-10950868|pmid-9670034|pmid-18922789|pmid-19028869|pmid-18541674|pmid-15155581 | We speculate that G1-specific mechanisms restrain signaling in response to a single DSB such as G1-specific phosphatases or inhibitors. | [
"16",
"54",
"34",
"34",
"55",
"35",
"43",
"44",
"56",
"43",
"44",
"57",
"58",
"59",
"60"
] | 135 | 43,494 | 0 | false | We speculate that G1-specific mechanisms restrain signaling in response to a single DSB such as G1-specific phosphatases or inhibitors. | [] | We speculate that G1-specific mechanisms restrain signaling in response to a single DSB such as G1-specific phosphatases or inhibitors. | true | true | true | true | true | 7,526 |
4 | DISCUSSION | 1 | 15 | [
"B15",
"B16",
"B34",
"B35",
"B35",
"B61",
"B62"
] | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | Consistent with previous observations (15,16,34,35), Rad53 (as well as the Dun1 and Chk1) is not detectably activated by a single HO-mediated DSB in G1-arrested cells. | [
"15",
"16",
"34",
"35",
"35",
"61",
"62"
] | 167 | 43,495 | 0 | false | Consistent with previous observations, Rad53 (as well as the Dun1 and Chk1) is not detectably activated by a single HO-mediated DSB in G1-arrested cells. | [
"15,16,34,35"
] | Consistent with previous observations, Rad53 is not detectably activated by a single HO-mediated DSB in G1-arrested cells. | true | true | true | true | true | 7,527 |
4 | DISCUSSION | 1 | 15 | [
"B15",
"B16",
"B34",
"B35",
"B35",
"B61",
"B62"
] | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | It is impossible to distinguish whether these kinases are truly not activated or activated to low level that eludes detection by the standard assays employed here and in the other studies. | [
"15",
"16",
"34",
"35",
"35",
"61",
"62"
] | 188 | 43,496 | 0 | false | It is impossible to distinguish whether these kinases are truly not activated or activated to low level that eludes detection by the standard assays employed here and in the other studies. | [] | It is impossible to distinguish whether these kinases are truly not activated or activated to low level that eludes detection by the standard assays employed here and in the other studies. | true | true | true | true | true | 7,527 |
4 | DISCUSSION | 1 | 15 | [
"B15",
"B16",
"B34",
"B35",
"B35",
"B61",
"B62"
] | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | Barlow et al. | [
"15",
"16",
"34",
"35",
"35",
"61",
"62"
] | 13 | 43,497 | 0 | false | Barlow et al. | [] | Barlow et al. | true | true | true | true | true | 7,527 |
4 | DISCUSSION | 1 | 35 | [
"B15",
"B16",
"B34",
"B35",
"B35",
"B61",
"B62"
] | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | (35) observed that the ribonucleotide reductase inhibitor Sml1 was degraded in 20% of G1-arrested cells experiencing a single I-SceI induced DSB without detectable Rad53 activation, leading the authors to suggest that Sml1 degradation was a more sensitive measure of DDR activation than Rad53 kinase activation. | [
"15",
"16",
"34",
"35",
"35",
"61",
"62"
] | 311 | 43,498 | 1 | false | observed that the ribonucleotide reductase inhibitor Sml1 was degraded in 20% of G1-arrested cells experiencing a single I-SceI induced DSB without detectable Rad53 activation, leading the authors to suggest that Sml1 degradation was a more sensitive measure of DDR activation than Rad53 kinase activation. | [
"35"
] | observed that the ribonucleotide reductase inhibitor Sml1 was degraded in 20% of G1-arrested cells experiencing a single I-SceI induced DSB without detectable Rad53 activation, leading the authors to suggest that Sml1 degradation was a more sensitive measure of DDR activation than Rad53 kinase activation. | false | true | true | true | false | 7,527 |
4 | DISCUSSION | 1 | 61 | [
"B15",
"B16",
"B34",
"B35",
"B35",
"B61",
"B62"
] | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | Degradation of Sml1 is triggered by phosphorylation by Dun1 kinase (61), but it is possible that in G1-arrested cells also Mec1 kinase targets Sml1. | [
"15",
"16",
"34",
"35",
"35",
"61",
"62"
] | 148 | 43,499 | 1 | false | Degradation of Sml1 is triggered by phosphorylation by Dun1 kinase, but it is possible that in G1-arrested cells also Mec1 kinase targets Sml1. | [
"61"
] | Degradation of Sml1 is triggered by phosphorylation by Dun1 kinase, but it is possible that in G1-arrested cells also Mec1 kinase targets Sml1. | true | true | true | true | true | 7,527 |
4 | DISCUSSION | 1 | 62 | [
"B15",
"B16",
"B34",
"B35",
"B35",
"B61",
"B62"
] | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | In addition, there is evidence that Dun1 can be activated in Rad53-independent fashion (62). | [
"15",
"16",
"34",
"35",
"35",
"61",
"62"
] | 92 | 43,500 | 1 | false | In addition, there is evidence that Dun1 can be activated in Rad53-independent fashion. | [
"62"
] | In addition, there is evidence that Dun1 can be activated in Rad53-independent fashion. | true | true | true | true | true | 7,527 |
4 | DISCUSSION | 1 | 15 | [
"B15",
"B16",
"B34",
"B35",
"B35",
"B61",
"B62"
] | 20,061,370 | pmid-11239458|pmid-15496928|pmid-18511906|pmid-18406328|pmid-18406328|pmid-11904430|pmid-12556502 | Collectively, these observations provide evidence that DNA-damage-signaling in G1 cells is different from other phases of the cell cycle, whether this involves no kinase activation downstream of Mec1 (as suggested in Supplementary Figure S2) or a low level of activation of the effector kinases (not detectable by the pr... | [
"15",
"16",
"34",
"35",
"35",
"61",
"62"
] | 366 | 43,501 | 0 | false | Collectively, these observations provide evidence that DNA-damage-signaling in G1 cells is different from other phases of the cell cycle, whether this involves no kinase activation downstream of Mec1 (as suggested in Supplementary Figure S2) or a low level of activation of the effector kinases (not detectable by the pr... | [] | Collectively, these observations provide evidence that DNA-damage-signaling in G1 cells is different from other phases of the cell cycle, whether this involves no kinase activation downstream of Mec1 (as suggested in Supplementary Figure S2) or a low level of activation of the effector kinases (not detectable by the pr... | true | true | true | true | true | 7,527 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | The polybrominated diphenyl ethers (PBDEs) including penta-BDE and deca-BDE (Fig. | [
"1",
"2",
"3",
"4"
] | 81 | 43,502 | 0 | false | The polybrominated diphenyl ethers (PBDEs) including penta-BDE and deca-BDE (Fig. | [] | The polybrominated diphenyl ethers (PBDEs) including penta-BDE and deca-BDE (Fig. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | 1) are used in household plastic products, such as, children's toys, textiles, electronic, and furniture. | [
"1",
"2",
"3",
"4"
] | 105 | 43,503 | 0 | false | 1) are used in household plastic products, such as, children's toys, textiles, electronic, and furniture. | [] | 1) are used in household plastic products, such as, children's toys, textiles, electronic, and furniture. | false | false | true | true | false | 7,528 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | Toxic effects of surrounding PBDEs on animals and human have been reported, and exposure to PBDEs as endocrine disruptors produces reproductive, developmental, and teratogenic toxicity, alterations in the thyroid hormone status, hepatotoxicity, teratogenicity, carcinogenicity, neurotoxicity, and immunotoxicity. | [
"1",
"2",
"3",
"4"
] | 312 | 43,504 | 0 | false | Toxic effects of surrounding PBDEs on animals and human have been reported, and exposure to PBDEs as endocrine disruptors produces reproductive, developmental, and teratogenic toxicity, alterations in the thyroid hormone status, hepatotoxicity, teratogenicity, carcinogenicity, neurotoxicity, and immunotoxicity. | [] | Toxic effects of surrounding PBDEs on animals and human have been reported, and exposure to PBDEs as endocrine disruptors produces reproductive, developmental, and teratogenic toxicity, alterations in the thyroid hormone status, hepatotoxicity, teratogenicity, carcinogenicity, neurotoxicity, and immunotoxicity. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | In recent, several studies demonstrating the immunotoxic effects of PBDEs on the development of immune system have been conducted. | [
"1",
"2",
"3",
"4"
] | 130 | 43,505 | 0 | false | In recent, several studies demonstrating the immunotoxic effects of PBDEs on the development of immune system have been conducted. | [] | In recent, several studies demonstrating the immunotoxic effects of PBDEs on the development of immune system have been conducted. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | The main findings published so far are changes in liver weight accompanied by histological alterations in animals given relatively large doses (1). | [
"1",
"2",
"3",
"4"
] | 147 | 43,506 | 1 | false | The main findings published so far are changes in liver weight accompanied by histological alterations in animals given relatively large doses. | [
"1"
] | The main findings published so far are changes in liver weight accompanied by histological alterations in animals given relatively large doses. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | In mice, the exposure of animals to PBDEs reduced the total number of splenocytes as well as splenic CD45R+, CD4+ and CD8+ cells. | [
"1",
"2",
"3",
"4"
] | 129 | 43,507 | 0 | false | In mice, the exposure of animals to PBDEs reduced the total number of splenocytes as well as splenic CD45R+, CD4+ and CD8+ cells. | [] | In mice, the exposure of animals to PBDEs reduced the total number of splenocytes as well as splenic CD45R+, CD4+ and CD8+ cells. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 2 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | IgG production in vitro by splenocytes from mice exposed to PBDE was significantly lower (2). | [
"1",
"2",
"3",
"4"
] | 93 | 43,508 | 1 | false | IgG production in vitro by splenocytes from mice exposed to PBDE was significantly lower. | [
"2"
] | IgG production in vitro by splenocytes from mice exposed to PBDE was significantly lower. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 3 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | Significant suppression of the anti-sheep red blood cell response was shown only in mice exposed subchronically to PBDE and also PBDE exposure resulted in decreased thymus weight (3). | [
"1",
"2",
"3",
"4"
] | 183 | 43,509 | 1 | false | Significant suppression of the anti-sheep red blood cell response was shown only in mice exposed subchronically to PBDE and also PBDE exposure resulted in decreased thymus weight. | [
"3"
] | Significant suppression of the anti-sheep red blood cell response was shown only in mice exposed subchronically to PBDE and also PBDE exposure resulted in decreased thymus weight. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | In immunotoxicity of PBDEs on twenty-week-old mink, mink given 5 and 10 ppm treatments exhibited significantly increased production of antibody compared to control mink. | [
"1",
"2",
"3",
"4"
] | 169 | 43,510 | 0 | false | In immunotoxicity of PBDEs on twenty-week-old mink, mink given 5 and 10 ppm treatments exhibited significantly increased production of antibody compared to control mink. | [] | In immunotoxicity of PBDEs on twenty-week-old mink, mink given 5 and 10 ppm treatments exhibited significantly increased production of antibody compared to control mink. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | Spleens of mink exposed to 10 ppm of the pentabrominated diphenyl ether mixture, DE-71, had significantly increased germinal center development and incidence of B-cell hyperplasia. | [
"1",
"2",
"3",
"4"
] | 180 | 43,511 | 0 | false | Spleens of mink exposed to 10 ppm of the pentabrominated diphenyl ether mixture, DE-71, had significantly increased germinal center development and incidence of B-cell hyperplasia. | [] | Spleens of mink exposed to 10 ppm of the pentabrominated diphenyl ether mixture, DE-71, had significantly increased germinal center development and incidence of B-cell hyperplasia. | true | true | true | true | true | 7,528 |
0 | INTRODUCTION | 1 | 4 | [
"B1",
"B2",
"B3",
"B4"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | The change on hematocrit, increase of percentage neutrophils and decrease of percentage were shown (4). | [
"1",
"2",
"3",
"4"
] | 103 | 43,512 | 1 | false | The change on hematocrit, increase of percentage neutrophils and decrease of percentage were shown. | [
"4"
] | The change on hematocrit, increase of percentage neutrophils and decrease of percentage were shown. | true | true | true | true | true | 7,528 |
1 | INTRODUCTION | 0 | null | null | 20,532,126 | null | These studies were undertaken to examine the immunological effects of penta-BDE and deca-BDE on the immune system of the dams. | null | 126 | 43,513 | 0 | false | null | null | These studies were undertaken to examine the immunological effects of penta-BDE and deca-BDE on the immune system of the dams. | true | true | true | true | true | 7,529 |
1 | INTRODUCTION | 0 | null | null | 20,532,126 | null | Moreover, it was addressed whether exposure to penta-BDE or deca-BDE on the dams affected on the developmental immune system of the offsprings in this study. | null | 157 | 43,514 | 0 | false | null | null | Moreover, it was addressed whether exposure to penta-BDE or deca-BDE on the dams affected on the developmental immune system of the offsprings in this study. | true | true | true | true | true | 7,529 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B9",
"B10",
"B12",
"B13",
"B14"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | Polybrominated diphenyl ethers (PBDEs) have been used as a flame retardant. | [
"5",
"9",
"10",
"12",
"13",
"14"
] | 75 | 43,515 | 0 | false | Polybrominated diphenyl ethers (PBDEs) have been used as a flame retardant. | [] | Polybrominated diphenyl ethers (PBDEs) have been used as a flame retardant. | true | true | true | true | true | 7,530 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B9",
"B10",
"B12",
"B13",
"B14"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | PBDEs have similar chemical structure to PCBs and dioxins with many similar chemical characteristics, and so have been suspected of being hazardous to humans, endocrine disruptors, etc (5-9). | [
"5",
"9",
"10",
"12",
"13",
"14"
] | 191 | 43,516 | 0 | false | PBDEs have similar chemical structure to PCBs and dioxins with many similar chemical characteristics, and so have been suspected of being hazardous to humans, endocrine disruptors, etc. | [
"5-9"
] | PBDEs have similar chemical structure to PCBs and dioxins with many similar chemical characteristics, and so have been suspected of being hazardous to humans, endocrine disruptors, etc. | true | true | true | true | true | 7,530 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B9",
"B10",
"B12",
"B13",
"B14"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | While penta-BDE has been banned in E.U. | [
"5",
"9",
"10",
"12",
"13",
"14"
] | 39 | 43,517 | 0 | false | While penta-BDE has been banned in E.U. | [] | While penta-BDE has been banned in E.U. | true | true | true | true | true | 7,530 |
0 | DISCUSSION | 1 | 13 | [
"B5",
"B9",
"B10",
"B12",
"B13",
"B14"
] | 20,532,126 | pmid-9067487|NA|pmid-8134923|pmid-17521147|pmid-12520400|pmid-9175843|NA|NA|pmid-12850100|NA | nations and in California because of greatest bioavailable concentrations in the environment (10-12), deca-BDE mixture makes up over 80% of the global PBDE market (13). | [
"5",
"9",
"10",
"12",
"13",
"14"
] | 168 | 43,518 | 1 | false | nations and in California because of greatest bioavailable concentrations in the environment, deca-BDE mixture makes up over 80% of the global PBDE market. | [
"10-12",
"13"
] | nations and in California because of greatest bioavailable concentrations in the environment, deca-BDE mixture makes up over 80% of the global PBDE market. | false | true | true | true | false | 7,530 |
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