paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5 | DISCUSSION | 1 | 41 | [
"DDQ002C41",
"DDQ002C42",
"DDQ002C47",
"DDQ002C47",
"DDQ002C47"
] | 20,053,669 | pmid-11750097|pmid-15704001|pmid-16055927|pmid-16055927|pmid-16055927 | As a functional J or J-like domain is essential for the formation of a stable heterodimer, we predict that the truncated protein is defective in forming a functional Magmas:DnaJC19 subcomplex and hence, the interaction of DnaJC19 with human TIM23 complex gets compromised. | [
"41",
"42",
"47",
"47",
"47"
] | 272 | 37,416 | 0 | false | As a functional J or J-like domain is essential for the formation of a stable heterodimer, we predict that the truncated protein is defective in forming a functional Magmas:DnaJC19 subcomplex and hence, the interaction of DnaJC19 with human TIM23 complex gets compromised. | [] | As a functional J or J-like domain is essential for the formation of a stable heterodimer, we predict that the truncated protein is defective in forming a functional Magmas:DnaJC19 subcomplex and hence, the interaction of DnaJC19 with human TIM23 complex gets compromised. | true | true | true | true | true | 6,412 |
5 | DISCUSSION | 1 | 41 | [
"DDQ002C41",
"DDQ002C42",
"DDQ002C47",
"DDQ002C47",
"DDQ002C47"
] | 20,053,669 | pmid-11750097|pmid-15704001|pmid-16055927|pmid-16055927|pmid-16055927 | This leads to the deregulation of import motor activity causing improper protein import thereby, affecting mitochondria biogenesis and cellular respiration. | [
"41",
"42",
"47",
"47",
"47"
] | 156 | 37,417 | 0 | false | This leads to the deregulation of import motor activity causing improper protein import thereby, affecting mitochondria biogenesis and cellular respiration. | [] | This leads to the deregulation of import motor activity causing improper protein import thereby, affecting mitochondria biogenesis and cellular respiration. | true | true | true | true | true | 6,412 |
5 | DISCUSSION | 1 | 41 | [
"DDQ002C41",
"DDQ002C42",
"DDQ002C47",
"DDQ002C47",
"DDQ002C47"
] | 20,053,669 | pmid-11750097|pmid-15704001|pmid-16055927|pmid-16055927|pmid-16055927 | The consequent impairment of energy metabolism in the cell especially in mitochondria-rich cardiac and neuronal tissues results in symptoms such as cardiomyopathy, peripheral neurodegeneration and ataxia. | [
"41",
"42",
"47",
"47",
"47"
] | 204 | 37,418 | 0 | false | The consequent impairment of energy metabolism in the cell especially in mitochondria-rich cardiac and neuronal tissues results in symptoms such as cardiomyopathy, peripheral neurodegeneration and ataxia. | [] | The consequent impairment of energy metabolism in the cell especially in mitochondria-rich cardiac and neuronal tissues results in symptoms such as cardiomyopathy, peripheral neurodegeneration and ataxia. | true | true | true | true | true | 6,412 |
5 | DISCUSSION | 1 | 41 | [
"DDQ002C41",
"DDQ002C42",
"DDQ002C47",
"DDQ002C47",
"DDQ002C47"
] | 20,053,669 | pmid-11750097|pmid-15704001|pmid-16055927|pmid-16055927|pmid-16055927 | However, the relevance of upregulated Magmas levels other than protein import function is not well established, underlines the importance of future investigation. | [
"41",
"42",
"47",
"47",
"47"
] | 162 | 37,419 | 0 | false | However, the relevance of upregulated Magmas levels other than protein import function is not well established, underlines the importance of future investigation. | [] | However, the relevance of upregulated Magmas levels other than protein import function is not well established, underlines the importance of future investigation. | true | true | true | true | true | 6,412 |
0 | DISCUSSION | 0 | null | null | 19,401,418 | null | Our experiments show for the first time that SK4 channels participate in the regulation of β-cell function and glucose homeostasis in vivo. | null | 139 | 37,420 | 0 | false | null | null | Our experiments show for the first time that SK4 channels participate in the regulation of β-cell function and glucose homeostasis in vivo. | true | true | true | true | true | 6,413 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | Glucose-induced insulin secretion involves tight coupling of glucose metabolism, electrical activity, [Ca2+]c, and exocytosis. | [
"46",
"47",
"33",
"48",
"34"
] | 126 | 37,421 | 0 | false | Glucose-induced insulin secretion involves tight coupling of glucose metabolism, electrical activity, [Ca2+]c, and exocytosis. | [] | Glucose-induced insulin secretion involves tight coupling of glucose metabolism, electrical activity, [Ca2+]c, and exocytosis. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | The key event linking glucose metabolism to membrane depolarization is the closure of KATP channels. | [
"46",
"47",
"33",
"48",
"34"
] | 100 | 37,422 | 0 | false | The key event linking glucose metabolism to membrane depolarization is the closure of KATP channels. | [] | The key event linking glucose metabolism to membrane depolarization is the closure of KATP channels. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | Subsequent opening of L-type Ca2+ channels increases [Ca2+]c, representing the triggering signal for insulin release (46,47). | [
"46",
"47",
"33",
"48",
"34"
] | 125 | 37,423 | 0 | false | Subsequent opening of L-type Ca2+ channels increases [Ca2+]c, representing the triggering signal for insulin release. | [
"46,47"
] | Subsequent opening of L-type Ca2+ channels increases [Ca2+]c, representing the triggering signal for insulin release. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | Our data show that SK4 channel protein is expressed in murine pancreatic islets. | [
"46",
"47",
"33",
"48",
"34"
] | 80 | 37,424 | 0 | false | Our data show that SK4 channel protein is expressed in murine pancreatic islets. | [] | Our data show that SK4 channel protein is expressed in murine pancreatic islets. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | SK4 channels are operative in β-cells and constitute an important regulator of stimulus-secretion coupling. | [
"46",
"47",
"33",
"48",
"34"
] | 107 | 37,425 | 0 | false | SK4 channels are operative in β-cells and constitute an important regulator of stimulus-secretion coupling. | [] | SK4 channels are operative in β-cells and constitute an important regulator of stimulus-secretion coupling. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | In WT β-cells, pharmacological opening or closure of SK4 channels crucially alters Vm (Figs. | [
"46",
"47",
"33",
"48",
"34"
] | 92 | 37,426 | 0 | false | In WT β-cells, pharmacological opening or closure of SK4 channels crucially alters Vm (Figs. | [] | In WT β-cells, pharmacological opening or closure of SK4 channels crucially alters Vm (Figs. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | Importantly, the SK4 channel blocker TRAM-34 depolarizes Vm and induces electrical activity at a subthreshold glucose concentration, thus enhancing the glucose effect on stimulus-secretion coupling (Fig. | [
"46",
"47",
"33",
"48",
"34"
] | 203 | 37,427 | 0 | false | Importantly, the SK4 channel blocker TRAM-34 depolarizes Vm and induces electrical activity at a subthreshold glucose concentration, thus enhancing the glucose effect on stimulus-secretion coupling (Fig. | [] | Importantly, the SK4 channel blocker TRAM-34 depolarizes Vm and induces electrical activity at a subthreshold glucose concentration, thus enhancing the glucose effect on stimulus-secretion coupling (Fig. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | This is of considerable significance, since it demonstrates that SK4 channels contribute to regulation of insulin release in the narrow range around the threshold blood glucose concentration physiologically relevant for glycemic control. | [
"46",
"47",
"33",
"48",
"34"
] | 237 | 37,428 | 0 | false | This is of considerable significance, since it demonstrates that SK4 channels contribute to regulation of insulin release in the narrow range around the threshold blood glucose concentration physiologically relevant for glycemic control. | [] | This is of considerable significance, since it demonstrates that SK4 channels contribute to regulation of insulin release in the narrow range around the threshold blood glucose concentration physiologically relevant for glycemic control. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | In addition, TRAM-34 and SK4-KO significantly reduce Kslow currents that are thought to participate in the characteristic burst pattern of pancreatic β-cells. | [
"46",
"47",
"33",
"48",
"34"
] | 158 | 37,429 | 0 | false | In addition, TRAM-34 and SK4-KO significantly reduce Kslow currents that are thought to participate in the characteristic burst pattern of pancreatic β-cells. | [] | In addition, TRAM-34 and SK4-KO significantly reduce Kslow currents that are thought to participate in the characteristic burst pattern of pancreatic β-cells. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | Our observation that SK4 is one component of Kslow (Fig. | [
"46",
"47",
"33",
"48",
"34"
] | 56 | 37,430 | 0 | false | Our observation that SK4 is one component of Kslow (Fig. | [] | Our observation that SK4 is one component of Kslow (Fig. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | 2E) emphasizes the importance of the SK4 channel for β-cell electrical activity. | [
"46",
"47",
"33",
"48",
"34"
] | 80 | 37,431 | 0 | false | 2E) emphasizes the importance of the SK4 channel for β-cell electrical activity. | [] | 2E) emphasizes the importance of the SK4 channel for β-cell electrical activity. | false | false | true | true | false | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | Although the involvement of SK4 in Kslow generation is evidenced by the reduced current in SK4-KO β-cells and in TRAM-34–treated WT cells, charybdotoxin failed to affect Kslow. | [
"46",
"47",
"33",
"48",
"34"
] | 176 | 37,432 | 0 | false | Although the involvement of SK4 in Kslow generation is evidenced by the reduced current in SK4-KO β-cells and in TRAM-34–treated WT cells, charybdotoxin failed to affect Kslow. | [] | Although the involvement of SK4 in Kslow generation is evidenced by the reduced current in SK4-KO β-cells and in TRAM-34–treated WT cells, charybdotoxin failed to affect Kslow. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 33 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | This observation requires further investigation but is in agreement with reports of others (33) describing inefficiency of the scorpion toxin on Kslow or on whole-cell currents with SK4 characteristics (48). | [
"46",
"47",
"33",
"48",
"34"
] | 207 | 37,433 | 1 | false | This observation requires further investigation but is in agreement with reports of others describing inefficiency of the scorpion toxin on Kslow or on whole-cell currents with SK4 characteristics. | [
"33",
"48"
] | This observation requires further investigation but is in agreement with reports of others describing inefficiency of the scorpion toxin on Kslow or on whole-cell currents with SK4 characteristics. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | Importantly, the typical oscillations of glucose-stimulated β-cells are not prevented by SK4-KO, and Kslow is not completely absent in SK4-KO β-cells, even in the presence of 1 mmol/l tolbutamide. | [
"46",
"47",
"33",
"48",
"34"
] | 196 | 37,434 | 0 | false | Importantly, the typical oscillations of glucose-stimulated β-cells are not prevented by SK4-KO, and Kslow is not completely absent in SK4-KO β-cells, even in the presence of 1 mmol/l tolbutamide. | [] | Importantly, the typical oscillations of glucose-stimulated β-cells are not prevented by SK4-KO, and Kslow is not completely absent in SK4-KO β-cells, even in the presence of 1 mmol/l tolbutamide. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 46 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | This suggests, in agreement with what has previously been proposed by Kanno et al. | [
"46",
"47",
"33",
"48",
"34"
] | 82 | 37,435 | 0 | false | This suggests, in agreement with what has previously been proposed by Kanno et al. | [] | This suggests, in agreement with what has previously been proposed by Kanno et al. | true | true | true | true | true | 6,414 |
1 | DISCUSSION | 1 | 34 | [
"B46",
"B47",
"B33",
"B48",
"B34"
] | 19,401,418 | pmid-2484976|pmid-8550572|pmid-10578013|pmid-9575286|pmid-12456829 | (34), that KATP channels, SK4, and other KCa channels act in concert to regulate the bursting activity of pancreatic β-cells. | [
"46",
"47",
"33",
"48",
"34"
] | 125 | 37,436 | 1 | false | , that KATP channels, SK4, and other KCa channels act in concert to regulate the bursting activity of pancreatic β-cells. | [
"34"
] | , that KATP channels, SK4, and other KCa channels act in concert to regulate the bursting activity of pancreatic β-cells. | false | false | true | true | false | 6,414 |
2 | DISCUSSION | 0 | null | null | 19,401,418 | null | SK4-KO did not affect blood glucose concentration of fed or fasted mice, demonstrating that glucose homeostasis can be maintained by other factors, e.g., adaptation in central regulation of energy balance or activation of peripheral counterregulatory mechanisms. | null | 262 | 37,437 | 0 | false | null | null | SK4-KO did not affect blood glucose concentration of fed or fasted mice, demonstrating that glucose homeostasis can be maintained by other factors, e.g., adaptation in central regulation of energy balance or activation of peripheral counterregulatory mechanisms. | true | true | true | true | true | 6,415 |
2 | DISCUSSION | 0 | null | null | 19,401,418 | null | However, SK4-KO improved the glucose tolerance after glucose challenge, whereas insulin sensitivity remained unchanged (Fig. | null | 124 | 37,438 | 0 | false | null | null | However, SK4-KO improved the glucose tolerance after glucose challenge, whereas insulin sensitivity remained unchanged (Fig. | true | true | true | true | true | 6,415 |
2 | DISCUSSION | 0 | null | null | 19,401,418 | null | This strongly suggests that the β-cell is the major target of SK4-KO with regard to glycemic control. | null | 101 | 37,439 | 0 | false | null | null | This strongly suggests that the β-cell is the major target of SK4-KO with regard to glycemic control. | true | true | true | true | true | 6,415 |
2 | DISCUSSION | 0 | null | null | 19,401,418 | null | Indeed, SK4-KO β-cells displayed alterations in agreement with improved glucose tolerance: in glucose-stimulated SK4-KO β-cells, the plateau potential was more depolarized compared with WT cells. | null | 195 | 37,440 | 0 | false | null | null | Indeed, SK4-KO β-cells displayed alterations in agreement with improved glucose tolerance: in glucose-stimulated SK4-KO β-cells, the plateau potential was more depolarized compared with WT cells. | true | true | true | true | true | 6,415 |
2 | DISCUSSION | 0 | null | null | 19,401,418 | null | Consequently, the frequency of Ca2+ APs was increased by ∼30%. | null | 62 | 37,441 | 0 | false | null | null | Consequently, the frequency of Ca2+ APs was increased by ∼30%. | true | true | true | true | true | 6,415 |
2 | DISCUSSION | 0 | null | null | 19,401,418 | null | In addition, loss or blockade of SK4 channels resulted in AP broadening and elevated Ca2+ influx. | null | 97 | 37,442 | 0 | false | null | null | In addition, loss or blockade of SK4 channels resulted in AP broadening and elevated Ca2+ influx. | true | true | true | true | true | 6,415 |
2 | DISCUSSION | 0 | null | null | 19,401,418 | null | These effects are suited to enhance exocytosis and finally to improve glucose tolerance. | null | 88 | 37,443 | 0 | false | null | null | These effects are suited to enhance exocytosis and finally to improve glucose tolerance. | true | true | true | true | true | 6,415 |
3 | DISCUSSION | 1 | 49 | [
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] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | For control of insulin secretion, the concentration-response correlation of glucose and electrical activity is very important (49). | [
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] | 131 | 37,444 | 1 | false | For control of insulin secretion, the concentration-response correlation of glucose and electrical activity is very important. | [
"49"
] | For control of insulin secretion, the concentration-response correlation of glucose and electrical activity is very important. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
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"B46",
"B2",
"B52",
"B53",
"B52",
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] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | SK4-KO induced a clear left shift in glucose responsiveness with respect to Vm, [Ca2+]c, and insulin secretion (Fig. | [
"49",
"50",
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"46",
"2",
"52",
"53",
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] | 116 | 37,445 | 0 | false | SK4-KO induced a clear left shift in glucose responsiveness with respect to Vm, c, and insulin secretion (Fig. | [
"Ca2+"
] | SK4-KO induced a clear left shift in glucose responsiveness with respect to Vm, c, and insulin secretion (Fig. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | Furthermore, electrical activity could be induced by TRAM-34 applied to subthreshold glucose concentrations, i.e., when Vm is already depolarized but has not reached the threshold for Ca2+ APs (Fig. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 198 | 37,446 | 0 | false | Furthermore, electrical activity could be induced by TRAM-34 applied to subthreshold glucose concentrations, i.e., when Vm is already depolarized but has not reached the threshold for Ca2+ APs (Fig. | [] | Furthermore, electrical activity could be induced by TRAM-34 applied to subthreshold glucose concentrations, i.e., when Vm is already depolarized but has not reached the threshold for Ca2+ APs (Fig. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
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] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | It is well-known that the resting membrane potential of β-cells is predominantly carried by KATP current (50,51). | [
"49",
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"53",
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] | 113 | 37,447 | 0 | false | It is well-known that the resting membrane potential of β-cells is predominantly carried by KATP current. | [
"50,51"
] | It is well-known that the resting membrane potential of β-cells is predominantly carried by KATP current. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
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] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | In agreement, SK4-KO did not affect the responsiveness of β-cells at low glucose concentrations (Fig. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
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] | 101 | 37,448 | 0 | false | In agreement, SK4-KO did not affect the responsiveness of β-cells at low glucose concentrations (Fig. | [] | In agreement, SK4-KO did not affect the responsiveness of β-cells at low glucose concentrations (Fig. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
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] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | 3B) and TRAM-34 did not depolarize WT β-cells under resting conditions. | [
"49",
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"51",
"46",
"2",
"52",
"53",
"52",
"54",
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] | 71 | 37,449 | 0 | false | 3B) and TRAM-34 did not depolarize WT β-cells under resting conditions. | [] | 3B) and TRAM-34 did not depolarize WT β-cells under resting conditions. | false | false | true | true | false | 6,416 |
3 | DISCUSSION | 1 | 46 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
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] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | Regulation of insulin secretion occurs via a gradual decrease in the open probability of KATP channels in response to a stepwise elevation of glucose (46), thereby increasing membrane depolarization. | [
"49",
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"52",
"53",
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] | 199 | 37,450 | 1 | false | Regulation of insulin secretion occurs via a gradual decrease in the open probability of KATP channels in response to a stepwise elevation of glucose, thereby increasing membrane depolarization. | [
"46"
] | Regulation of insulin secretion occurs via a gradual decrease in the open probability of KATP channels in response to a stepwise elevation of glucose, thereby increasing membrane depolarization. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
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"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | SK4 channel opening is largely independent of Vm (2,52) but strictly regulated by [Ca2+]c. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 90 | 37,451 | 0 | false | SK4 channel opening is largely independent of Vm but strictly regulated by c. | [
"2,52",
"Ca2+"
] | SK4 channel opening is largely independent of Vm but strictly regulated by c. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 53 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | Half-maximal activation occurs at Ca2+ concentrations ranging from 300 to 500 nmol/l (53). | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 90 | 37,452 | 1 | false | Half-maximal activation occurs at Ca2+ concentrations ranging from 300 to 500 nmol/l. | [
"53"
] | Half-maximal activation occurs at Ca2+ concentrations ranging from 300 to 500 nmol/l. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 52 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | For myocytes, it has been shown that SK4 channels are already open when Ca2+ is reduced below 100 nmol/l (52). | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 110 | 37,453 | 1 | false | For myocytes, it has been shown that SK4 channels are already open when Ca2+ is reduced below 100 nmol/l. | [
"52"
] | For myocytes, it has been shown that SK4 channels are already open when Ca2+ is reduced below 100 nmol/l. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | This is in agreement with our observation that SK4 channel inhibition influences Vm under conditions where [Ca2+]c is in the low nanomoles per liter range. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 155 | 37,454 | 0 | false | This is in agreement with our observation that SK4 channel inhibition influences Vm under conditions where c is in the low nanomoles per liter range. | [
"Ca2+"
] | This is in agreement with our observation that SK4 channel inhibition influences Vm under conditions where c is in the low nanomoles per liter range. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 54 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | For pancreatic β-cells, it was suggested that Ca2+ influx via L-type Ca2+ channels does not increase at a Vm below −40 mV (54). | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 127 | 37,455 | 1 | false | For pancreatic β-cells, it was suggested that Ca2+ influx via L-type Ca2+ channels does not increase at a Vm below −40 mV. | [
"54"
] | For pancreatic β-cells, it was suggested that Ca2+ influx via L-type Ca2+ channels does not increase at a Vm below −40 mV. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | This might raise the question why SK4 channel inhibition does not affect Vm at 0.5 mmol/l glucose but initiates APs at 6 mmol/l glucose. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 136 | 37,456 | 0 | false | This might raise the question why SK4 channel inhibition does not affect Vm at 0.5 mmol/l glucose but initiates APs at 6 mmol/l glucose. | [] | This might raise the question why SK4 channel inhibition does not affect Vm at 0.5 mmol/l glucose but initiates APs at 6 mmol/l glucose. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | However, because Larsson-Nyrén et al. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 37 | 37,457 | 0 | false | However, because Larsson-Nyrén et al. | [] | However, because Larsson-Nyrén et al. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 54 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | (54) induced Ca2+ influx by short depolarizing voltage steps starting at −70 mV, they cannot elucidate whether a gradual increase of Vm elevates Ca2+ channel activity, thereby promoting Ca2+ influx even below the threshold for Ca2+ APs. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 236 | 37,458 | 1 | false | induced Ca2+ influx by short depolarizing voltage steps starting at −70 mV, they cannot elucidate whether a gradual increase of Vm elevates Ca2+ channel activity, thereby promoting Ca2+ influx even below the threshold for Ca2+ APs. | [
"54"
] | induced Ca2+ influx by short depolarizing voltage steps starting at −70 mV, they cannot elucidate whether a gradual increase of Vm elevates Ca2+ channel activity, thereby promoting Ca2+ influx even below the threshold for Ca2+ APs. | false | true | true | true | false | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | In this context, it is noteworthy that Nelson et al. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 52 | 37,459 | 0 | false | In this context, it is noteworthy that Nelson et al. | [] | In this context, it is noteworthy that Nelson et al. | true | true | true | true | true | 6,416 |
3 | DISCUSSION | 1 | 55 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | (55) demonstrated in cell-attached membrane patches of basilar arteries that the open probability of L-type Ca2+ channels already starts to increase at −65 mV, which is ∼20 mV more negative than the threshold potential for APs. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 227 | 37,460 | 1 | false | demonstrated in cell-attached membrane patches of basilar arteries that the open probability of L-type Ca2+ channels already starts to increase at −65 mV, which is ∼20 mV more negative than the threshold potential for APs. | [
"55"
] | demonstrated in cell-attached membrane patches of basilar arteries that the open probability of L-type Ca2+ channels already starts to increase at −65 mV, which is ∼20 mV more negative than the threshold potential for APs. | false | true | true | true | false | 6,416 |
3 | DISCUSSION | 1 | 49 | [
"B49",
"B50",
"B51",
"B46",
"B2",
"B52",
"B53",
"B52",
"B54",
"B54",
"B55"
] | 19,401,418 | NA|NA|pmid-2407553|pmid-2484976|pmid-9730970|pmid-9630695|pmid-16443824|pmid-9630695|NA|NA|pmid-2164782 | Consequently, glucose-regulated membrane depolarization might enhance SK4 channel activity dose dependently even before the threshold for induction of Ca2+ APs. | [
"49",
"50",
"51",
"46",
"2",
"52",
"53",
"52",
"54",
"54",
"55"
] | 160 | 37,461 | 0 | false | Consequently, glucose-regulated membrane depolarization might enhance SK4 channel activity dose dependently even before the threshold for induction of Ca2+ APs. | [] | Consequently, glucose-regulated membrane depolarization might enhance SK4 channel activity dose dependently even before the threshold for induction of Ca2+ APs. | true | true | true | true | true | 6,416 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | Our data suggest that membrane depolarization induced by closure of KATP channels leads to Ca2+ influx and subsequent activation of SK4 channels. | [
"5",
"56"
] | 145 | 37,462 | 0 | false | Our data suggest that membrane depolarization induced by closure of KATP channels leads to Ca2+ influx and subsequent activation of SK4 channels. | [] | Our data suggest that membrane depolarization induced by closure of KATP channels leads to Ca2+ influx and subsequent activation of SK4 channels. | true | true | true | true | true | 6,417 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | This mechanism counteracts the depolarization and promotes closure of L-type Ca2+ channels. | [
"5",
"56"
] | 91 | 37,463 | 0 | false | This mechanism counteracts the depolarization and promotes closure of L-type Ca2+ channels. | [] | This mechanism counteracts the depolarization and promotes closure of L-type Ca2+ channels. | true | true | true | true | true | 6,417 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | We hypothesize that modulation of β-cell activity via SK4 channels contributes to the precise adjustment of insulin secretion according to the current metabolic demands. | [
"5",
"56"
] | 169 | 37,464 | 0 | false | We hypothesize that modulation of β-cell activity via SK4 channels contributes to the precise adjustment of insulin secretion according to the current metabolic demands. | [] | We hypothesize that modulation of β-cell activity via SK4 channels contributes to the precise adjustment of insulin secretion according to the current metabolic demands. | true | true | true | true | true | 6,417 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | An important regulatory function of SK4 channels concerning intracellular Ca2+ homeostasis has also been described for other cellular systems. | [
"5",
"56"
] | 142 | 37,465 | 0 | false | An important regulatory function of SK4 channels concerning intracellular Ca2+ homeostasis has also been described for other cellular systems. | [] | An important regulatory function of SK4 channels concerning intracellular Ca2+ homeostasis has also been described for other cellular systems. | true | true | true | true | true | 6,417 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | In mast cells or in the endothelium, receptor-mediated Ca2+ influx activates SK4 channels, thereby inducing membrane hyperpolarization. | [
"5",
"56"
] | 135 | 37,466 | 0 | false | In mast cells or in the endothelium, receptor-mediated Ca2+ influx activates SK4 channels, thereby inducing membrane hyperpolarization. | [] | In mast cells or in the endothelium, receptor-mediated Ca2+ influx activates SK4 channels, thereby inducing membrane hyperpolarization. | true | true | true | true | true | 6,417 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | However, in contrast to pancreatic β-cells, the increased K+ conductance enforces Ca2+ influx in these cells through transient receptor potential or store-operated Ca2+ channels. | [
"5",
"56"
] | 178 | 37,467 | 0 | false | However, in contrast to pancreatic β-cells, the increased K+ conductance enforces Ca2+ influx in these cells through transient receptor potential or store-operated Ca2+ channels. | [] | However, in contrast to pancreatic β-cells, the increased K+ conductance enforces Ca2+ influx in these cells through transient receptor potential or store-operated Ca2+ channels. | true | true | true | true | true | 6,417 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | The final result is elevation of [Ca2+]c, which triggers mast cell degranulation or endothelium-mediated vasodilation, respectively (5,56). | [
"5",
"56"
] | 139 | 37,468 | 0 | false | The final result is elevation of [Ca2+]c, which triggers mast cell degranulation or endothelium-mediated vasodilation, respectively. | [
"5,56"
] | The final result is elevation of [Ca2+]c, which triggers mast cell degranulation or endothelium-mediated vasodilation, respectively. | true | true | true | true | true | 6,417 |
4 | DISCUSSION | 1 | 5 | [
"B5",
"B56"
] | 19,401,418 | pmid-18523267|pmid-16873714 | Depending on the pathway of Ca2+ influx, SK4 channel activation could either enhance or limit Ca2+-regulated signaling cascades in different tissues or organs. | [
"5",
"56"
] | 159 | 37,469 | 0 | false | Depending on the pathway of Ca2+ influx, SK4 channel activation could either enhance or limit Ca2+-regulated signaling cascades in different tissues or organs. | [] | Depending on the pathway of Ca2+ influx, SK4 channel activation could either enhance or limit Ca2+-regulated signaling cascades in different tissues or organs. | true | true | true | true | true | 6,417 |
5 | DISCUSSION | 1 | 57 | [
"B57",
"B58"
] | 19,401,418 | pmid-9989540|pmid-15305887 | As the Ca2+ dependence of SK4 channels is expected to couple channel activity to the metabolic status of pancreatic β-cells, SK4 channels may modulate cell function without bearing the risk for unwanted hypoglycemic episodes, which complicates the use of insulinotropic drugs acting on KATP channels (57,58). | [
"57",
"58"
] | 308 | 37,470 | 0 | false | As the Ca2+ dependence of SK4 channels is expected to couple channel activity to the metabolic status of pancreatic β-cells, SK4 channels may modulate cell function without bearing the risk for unwanted hypoglycemic episodes, which complicates the use of insulinotropic drugs acting on KATP channels. | [
"57,58"
] | As the Ca2+ dependence of SK4 channels is expected to couple channel activity to the metabolic status of pancreatic β-cells, SK4 channels may modulate cell function without bearing the risk for unwanted hypoglycemic episodes, which complicates the use of insulinotropic drugs acting on KATP channels. | true | true | true | true | true | 6,418 |
5 | DISCUSSION | 1 | 57 | [
"B57",
"B58"
] | 19,401,418 | pmid-9989540|pmid-15305887 | Importantly, SK4-KO mice displayed no signs of hypoglycemia after overnight fasting or when they were fed ad libitum, which shows that the genetic manipulation did not result in excessive insulin secretion per se but improved β-cell response when challenged with high blood glucose concentrations. | [
"57",
"58"
] | 297 | 37,471 | 0 | false | Importantly, SK4-KO mice displayed no signs of hypoglycemia after overnight fasting or when they were fed ad libitum, which shows that the genetic manipulation did not result in excessive insulin secretion per se but improved β-cell response when challenged with high blood glucose concentrations. | [] | Importantly, SK4-KO mice displayed no signs of hypoglycemia after overnight fasting or when they were fed ad libitum, which shows that the genetic manipulation did not result in excessive insulin secretion per se but improved β-cell response when challenged with high blood glucose concentrations. | true | true | true | true | true | 6,418 |
5 | DISCUSSION | 1 | 57 | [
"B57",
"B58"
] | 19,401,418 | pmid-9989540|pmid-15305887 | Because SK4-KO markedly elevated the proportion of active β-cells, it is suggested that a reduction of the SK4 current is a suitable tool to recruit more β-cells for nutrient-stimulated insulin release. | [
"57",
"58"
] | 202 | 37,472 | 0 | false | Because SK4-KO markedly elevated the proportion of active β-cells, it is suggested that a reduction of the SK4 current is a suitable tool to recruit more β-cells for nutrient-stimulated insulin release. | [] | Because SK4-KO markedly elevated the proportion of active β-cells, it is suggested that a reduction of the SK4 current is a suitable tool to recruit more β-cells for nutrient-stimulated insulin release. | true | true | true | true | true | 6,418 |
5 | DISCUSSION | 1 | 57 | [
"B57",
"B58"
] | 19,401,418 | pmid-9989540|pmid-15305887 | Thus, targeting SK4 channels pharmacologically might be a useful approach to augment insulin release in β-cells with impaired secretory response. | [
"57",
"58"
] | 145 | 37,473 | 0 | false | Thus, targeting SK4 channels pharmacologically might be a useful approach to augment insulin release in β-cells with impaired secretory response. | [] | Thus, targeting SK4 channels pharmacologically might be a useful approach to augment insulin release in β-cells with impaired secretory response. | true | true | true | true | true | 6,418 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B2",
"B3",
"B4"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | Long interspersed element-1, LINE-1 or L1, is an autonomous family of retroelements that is currently active in mammalian genomes (1). | [
"1",
"2",
"2",
"3",
"4"
] | 134 | 37,474 | 1 | false | Long interspersed element-1, LINE-1 or L1, is an autonomous family of retroelements that is currently active in mammalian genomes. | [
"1"
] | Long interspersed element-1, LINE-1 or L1, is an autonomous family of retroelements that is currently active in mammalian genomes. | true | true | true | true | true | 6,419 |
0 | INTRODUCTION | 1 | 2 | [
"B1",
"B2",
"B2",
"B3",
"B4"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | The human genome has accumulated about 500 000 L1 copies, amounting to 17% of genomic content (2). | [
"1",
"2",
"2",
"3",
"4"
] | 98 | 37,475 | 1 | false | The human genome has accumulated about 500 000 L1 copies, amounting to 17% of genomic content. | [
"2"
] | The human genome has accumulated about 500 000 L1 copies, amounting to 17% of genomic content. | true | true | true | true | true | 6,419 |
0 | INTRODUCTION | 1 | 2 | [
"B1",
"B2",
"B2",
"B3",
"B4"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | The majority of L1 inserts are 5′-truncated or rearranged (2); and as a result they are retrotranspositionally inactive. | [
"1",
"2",
"2",
"3",
"4"
] | 120 | 37,476 | 1 | false | The majority of L1 inserts are 5′-truncated or rearranged ; and as a result they are retrotranspositionally inactive. | [
"2"
] | The majority of L1 inserts are 5′-truncated or rearranged ; and as a result they are retrotranspositionally inactive. | true | true | true | true | true | 6,419 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B2",
"B3",
"B4"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | Approximately 3000 L1s in the human genome are full-length (i.e. | [
"1",
"2",
"2",
"3",
"4"
] | 64 | 37,477 | 0 | false | Approximately 3000 L1s in the human genome are full-length (i.e. | [] | Approximately 3000 L1s in the human genome are full-length (i.e. | true | true | true | true | true | 6,419 |
0 | INTRODUCTION | 1 | 3 | [
"B1",
"B2",
"B2",
"B3",
"B4"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | they contain 5′- and 3′-UTRs and sequences in between without major rearrangement), with about 150 containing both intact open reading frames (ORF) 1 and 2, and about 100 additional elements maintaining only intact ORF2 (3). | [
"1",
"2",
"2",
"3",
"4"
] | 224 | 37,478 | 1 | false | they contain 5′- and 3′-UTRs and sequences in between without major rearrangement), with about 150 containing both intact open reading frames (ORF) 1 and 2, and about 100 additional elements maintaining only intact ORF2. | [
"3"
] | they contain 5′- and 3′-UTRs and sequences in between without major rearrangement), with about 150 containing both intact open reading frames (ORF) 1 and 2, and about 100 additional elements maintaining only intact ORF2. | false | true | true | true | false | 6,419 |
0 | INTRODUCTION | 1 | 4 | [
"B1",
"B2",
"B2",
"B3",
"B4"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | Both ORFs are required for L1 retrotransposition in cultured cells (4). | [
"1",
"2",
"2",
"3",
"4"
] | 71 | 37,479 | 1 | false | Both ORFs are required for L1 retrotransposition in cultured cells. | [
"4"
] | Both ORFs are required for L1 retrotransposition in cultured cells. | true | true | true | true | true | 6,419 |
1 | INTRODUCTION | 1 | 5–7 | [
"B5 B6 B7",
"B8",
"B9",
"B10",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17",
"B18",
"B11",
"B19 B20 B21"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | L1 expression in the germ line and cells that are closely associated with the germ line has been previously reported (5–7). | [
"5–7",
"8",
"9",
"10",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"11",
"19–21"
] | 123 | 37,480 | 1 | false | L1 expression in the germ line and cells that are closely associated with the germ line has been previously reported. | [
"5–7"
] | L1 expression in the germ line and cells that are closely associated with the germ line has been previously reported. | true | true | true | true | true | 6,420 |
1 | INTRODUCTION | 1 | 10 | [
"B5 B6 B7",
"B8",
"B9",
"B10",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17",
"B18",
"B11",
"B19 B20 B21"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | It has been suggested that full-length L1 mRNA is expressed little, if at all, in somatic tissues (8,9), although it has generally been detected in somatic cells that underwent malignant transformation (10). | [
"5–7",
"8",
"9",
"10",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"11",
"19–21"
] | 207 | 37,481 | 1 | false | It has been suggested that full-length L1 mRNA is expressed little, if at all, in somatic tissues, although it has generally been detected in somatic cells that underwent malignant transformation. | [
"8,9",
"10"
] | It has been suggested that full-length L1 mRNA is expressed little, if at all, in somatic tissues, although it has generally been detected in somatic cells that underwent malignant transformation. | true | true | true | true | true | 6,420 |
1 | INTRODUCTION | 1 | 5–7 | [
"B5 B6 B7",
"B8",
"B9",
"B10",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17",
"B18",
"B11",
"B19 B20 B21"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | Recent reports have shown, in addition to the germ line, some L1 protein expression in vascular endothelial cells of human male gonads, L1 RNA expression in lymphoblastoid cell lines, and L1 mobilization in the brains of L1-transgenic mice (7,11,12). | [
"5–7",
"8",
"9",
"10",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"11",
"19–21"
] | 250 | 37,482 | 0 | false | Recent reports have shown, in addition to the germ line, some L1 protein expression in vascular endothelial cells of human male gonads, L1 RNA expression in lymphoblastoid cell lines, and L1 mobilization in the brains of L1-transgenic mice. | [
"7,11,12"
] | Recent reports have shown, in addition to the germ line, some L1 protein expression in vascular endothelial cells of human male gonads, L1 RNA expression in lymphoblastoid cell lines, and L1 mobilization in the brains of L1-transgenic mice. | true | true | true | true | true | 6,420 |
1 | INTRODUCTION | 1 | 13 | [
"B5 B6 B7",
"B8",
"B9",
"B10",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17",
"B18",
"B11",
"B19 B20 B21"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | Unmethylated L1 loci and L1 mobilization has been reported in normal human brain (13). | [
"5–7",
"8",
"9",
"10",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"11",
"19–21"
] | 86 | 37,483 | 1 | false | Unmethylated L1 loci and L1 mobilization has been reported in normal human brain. | [
"13"
] | Unmethylated L1 loci and L1 mobilization has been reported in normal human brain. | true | true | true | true | true | 6,420 |
1 | INTRODUCTION | 1 | 5–7 | [
"B5 B6 B7",
"B8",
"B9",
"B10",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17",
"B18",
"B11",
"B19 B20 B21"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | Because the vast majority of the L1 RNA is spliced and/or prematurely polyadenylated (14,15), detection of L1 proteins in a cell is not a reliable indicator of the retrotransposition potential. | [
"5–7",
"8",
"9",
"10",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"11",
"19–21"
] | 193 | 37,484 | 0 | false | Because the vast majority of the L1 RNA is spliced and/or prematurely polyadenylated, detection of L1 proteins in a cell is not a reliable indicator of the retrotransposition potential. | [
"14,15"
] | Because the vast majority of the L1 RNA is spliced and/or prematurely polyadenylated, detection of L1 proteins in a cell is not a reliable indicator of the retrotransposition potential. | true | true | true | true | true | 6,420 |
1 | INTRODUCTION | 1 | 16 | [
"B5 B6 B7",
"B8",
"B9",
"B10",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B17",
"B18",
"B11",
"B19 B20 B21"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | Endogenous L1 elements (16), L1 elements transiently expressed in primary cells (17,18), and in somatic cells of transgenic mice (11,19–21), are capable of retrotransposition indicating that there are no intrinsic molecular limitations for L1 protein activity specific to somatic cells. | [
"5–7",
"8",
"9",
"10",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"17",
"18",
"11",
"19–21"
] | 286 | 37,485 | 1 | false | Endogenous L1 elements, L1 elements transiently expressed in primary cells, and in somatic cells of transgenic mice, are capable of retrotransposition indicating that there are no intrinsic molecular limitations for L1 protein activity specific to somatic cells. | [
"16",
"17,18",
"11,19–21"
] | Endogenous L1 elements, L1 elements transiently expressed in primary cells, and in somatic cells of transgenic mice, are capable of retrotransposition indicating that there are no intrinsic molecular limitations for L1 protein activity specific to somatic cells. | true | true | true | true | true | 6,420 |
2 | INTRODUCTION | 1 | 4 | [
"B4",
"B22",
"B23",
"B24"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | There are a broad range of factors that lead to DNA damage, both in the germ line and somatic cells. | [
"4",
"22",
"23",
"24"
] | 100 | 37,486 | 0 | false | There are a broad range of factors that lead to DNA damage, both in the germ line and somatic cells. | [] | There are a broad range of factors that lead to DNA damage, both in the germ line and somatic cells. | true | true | true | true | true | 6,421 |
2 | INTRODUCTION | 1 | 4 | [
"B4",
"B22",
"B23",
"B24"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | There has been a significant focus on exogenous (i.e. | [
"4",
"22",
"23",
"24"
] | 53 | 37,487 | 0 | false | There has been a significant focus on exogenous (i.e. | [] | There has been a significant focus on exogenous (i.e. | true | true | true | true | true | 6,421 |
2 | INTRODUCTION | 1 | 4 | [
"B4",
"B22",
"B23",
"B24"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | radiation and chemicals), as well as endogenous [replication errors and reactive oxygen species (ROS)], sources of somatic DNA damage. | [
"4",
"22",
"23",
"24"
] | 134 | 37,488 | 0 | false | radiation and chemicals), as well as endogenous [replication errors and reactive oxygen species (ROS)], sources of somatic DNA damage. | [] | radiation and chemicals), as well as endogenous [replication errors and reactive oxygen species (ROS)], sources of somatic DNA damage. | false | true | true | true | false | 6,421 |
2 | INTRODUCTION | 1 | 4 | [
"B4",
"B22",
"B23",
"B24"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | As demonstrated by the disease causing in vivo integration events and tissue culture experiments, expression of the functional L1 elements in human cells results in integration events of L1 as well as its parasites, short interspersed elements (SINEs) and presumably SVA elements. | [
"4",
"22",
"23",
"24"
] | 280 | 37,489 | 0 | false | As demonstrated by the disease causing in vivo integration events and tissue culture experiments, expression of the functional L1 elements in human cells results in integration events of L1 as well as its parasites, short interspersed elements (SINEs) and presumably SVA elements. | [] | As demonstrated by the disease causing in vivo integration events and tissue culture experiments, expression of the functional L1 elements in human cells results in integration events of L1 as well as its parasites, short interspersed elements (SINEs) and presumably SVA elements. | true | true | true | true | true | 6,421 |
2 | INTRODUCTION | 1 | 4 | [
"B4",
"B22",
"B23",
"B24"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | While retrotransposition of L1 elements requires production of the full-length L1 mRNA that contains both functional ORF1 and ORF2 proteins (4), SINE retrotransposons (such as Alu elements) rely only on the production of the functional L1 ORF2 protein in tissue culture-based assays (22). | [
"4",
"22",
"23",
"24"
] | 288 | 37,490 | 1 | false | While retrotransposition of L1 elements requires production of the full-length L1 mRNA that contains both functional ORF1 and ORF2 proteins, SINE retrotransposons (such as Alu elements) rely only on the production of the functional L1 ORF2 protein in tissue culture-based assays. | [
"4",
"22"
] | While retrotransposition of L1 elements requires production of the full-length L1 mRNA that contains both functional ORF1 and ORF2 proteins, SINE retrotransposons (such as Alu elements) rely only on the production of the functional L1 ORF2 protein in tissue culture-based assays. | true | true | true | true | true | 6,421 |
2 | INTRODUCTION | 1 | 4 | [
"B4",
"B22",
"B23",
"B24"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | Alu retrotransposons have been much more successful than L1 in occupying the human genome (accumulating to over 1 000 000 copies) and causing over twice the number of diseases originated by L1 elements (23,24). | [
"4",
"22",
"23",
"24"
] | 210 | 37,491 | 0 | false | Alu retrotransposons have been much more successful than L1 in occupying the human genome (accumulating to over 1 000 000 copies) and causing over twice the number of diseases originated by L1 elements. | [
"23,24"
] | Alu retrotransposons have been much more successful than L1 in occupying the human genome (accumulating to over 1 000 000 copies) and causing over twice the number of diseases originated by L1 elements. | true | true | true | true | true | 6,421 |
2 | INTRODUCTION | 1 | 4 | [
"B4",
"B22",
"B23",
"B24"
] | 20,215,437 | pmid-8945518|pmid-12897783|pmid-18256243|pmid-15983781|pmid-18256243|pmid-11237011|pmid-11237011|pmid-14638329 | This difference in the total genomic copy number of L1 and Alu elements may come from the variation in the retrotransposition efficiency, post-insertional selection, or both. | [
"4",
"22",
"23",
"24"
] | 174 | 37,492 | 0 | false | This difference in the total genomic copy number of L1 and Alu elements may come from the variation in the retrotransposition efficiency, post-insertional selection, or both. | [] | This difference in the total genomic copy number of L1 and Alu elements may come from the variation in the retrotransposition efficiency, post-insertional selection, or both. | true | true | true | true | true | 6,421 |
3 | INTRODUCTION | 1 | 25–27 | [
"B25 B26 B27",
"B27",
"B28",
"B27",
"B25",
"B29"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | In addition to insertional mutagenesis, expression of the functional wild-type (wt) full-length L1, or L1 ORF2 protein alone, in human cancer cells induces DNA double-strand breaks (DSBs) (25–27) in great excess relative to the integration events detected under the same conditions (27). | [
"25–27",
"27",
"28",
"27",
"25",
"29"
] | 287 | 37,493 | 1 | false | In addition to insertional mutagenesis, expression of the functional wild-type (wt) full-length L1, or L1 ORF2 protein alone, in human cancer cells induces DNA double-strand breaks (DSBs) in great excess relative to the integration events detected under the same conditions. | [
"25–27",
"27"
] | In addition to insertional mutagenesis, expression of the functional wild-type (wt) full-length L1, or L1 ORF2 protein alone, in human cancer cells induces DNA double-strand breaks (DSBs) in great excess relative to the integration events detected under the same conditions. | true | true | true | true | true | 6,422 |
3 | INTRODUCTION | 1 | 25–27 | [
"B25 B26 B27",
"B27",
"B28",
"B27",
"B25",
"B29"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | DNA DSBs are known to be highly toxic and mutagenic even when repaired by the wt DNA repair machinery in mammals [reviewed in ref. | [
"25–27",
"27",
"28",
"27",
"25",
"29"
] | 130 | 37,494 | 0 | false | DNA DSBs are known to be highly toxic and mutagenic even when repaired by the wt DNA repair machinery in mammals [reviewed in ref. | [] | DNA DSBs are known to be highly toxic and mutagenic even when repaired by the wt DNA repair machinery in mammals [reviewed in ref. | true | true | true | true | true | 6,422 |
3 | INTRODUCTION | 1 | 25–27 | [
"B25 B26 B27",
"B27",
"B28",
"B27",
"B25",
"B29"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | The cellular response to DNA damage usually manifests itself in cell cycle arrest, cell death (apoptosis or necrosis), or senescence. | [
"25–27",
"27",
"28",
"27",
"25",
"29"
] | 133 | 37,495 | 0 | false | The cellular response to DNA damage usually manifests itself in cell cycle arrest, cell death (apoptosis or necrosis), or senescence. | [] | The cellular response to DNA damage usually manifests itself in cell cycle arrest, cell death (apoptosis or necrosis), or senescence. | true | true | true | true | true | 6,422 |
3 | INTRODUCTION | 1 | 27 | [
"B25 B26 B27",
"B27",
"B28",
"B27",
"B25",
"B29"
] | 20,215,437 | pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-11684443|pmid-16490214|pmid-16670018|pmid-18555620|pmid-1701022|pmid-7693554|pmid-18396111|pmid-16936727|pmid-16728505|pmid-16735504|pmid-16648136 | L1 expression in human cancer cells has been reported to induce cell cycle arrest (27) and apoptosis (25,29). | [
"25–27",
"27",
"28",
"27",
"25",
"29"
] | 109 | 37,496 | 1 | false | L1 expression in human cancer cells has been reported to induce cell cycle arrest and apoptosis. | [
"27",
"25,29"
] | L1 expression in human cancer cells has been reported to induce cell cycle arrest and apoptosis. | true | true | true | true | true | 6,422 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Because L1 expression can contribute to DNA damage not only through insertional mutagenesis but also via generation of DSBs, a better understanding of the expression patterns of endogenous L1 elements, particularly because of the complex processing of their mRNA (14,15,30), would provide a more complete picture of the ... | [
"14",
"15",
"30",
"23"
] | 357 | 37,497 | 0 | false | Because L1 expression can contribute to DNA damage not only through insertional mutagenesis but also via generation of DSBs, a better understanding of the expression patterns of endogenous L1 elements, particularly because of the complex processing of their mRNA, would provide a more complete picture of the potential s... | [
"14,15,30"
] | Because L1 expression can contribute to DNA damage not only through insertional mutagenesis but also via generation of DSBs, a better understanding of the expression patterns of endogenous L1 elements, particularly because of the complex processing of their mRNA, would provide a more complete picture of the potential s... | true | true | true | true | true | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Our data demonstrate ongoing L1 expression in a broad spectrum of normal human tissues including adult stem cells. | [
"14",
"15",
"30",
"23"
] | 114 | 37,498 | 0 | false | Our data demonstrate ongoing L1 expression in a broad spectrum of normal human tissues including adult stem cells. | [] | Our data demonstrate ongoing L1 expression in a broad spectrum of normal human tissues including adult stem cells. | true | true | true | true | true | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Both the expression levels and the L1 RNA processing vary dramatically among the tissues tested in this study. | [
"14",
"15",
"30",
"23"
] | 110 | 37,499 | 0 | false | Both the expression levels and the L1 RNA processing vary dramatically among the tissues tested in this study. | [] | Both the expression levels and the L1 RNA processing vary dramatically among the tissues tested in this study. | true | true | true | true | true | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | We provide experimental support that L1-related DNA damage in human somatic cells is not limited to the production of the full-length L1 mRNA because of the expression of the L1 splice transcript that likely contributes to the translation of the L1 ORF2 protein. | [
"14",
"15",
"30",
"23"
] | 262 | 37,500 | 0 | false | We provide experimental support that L1-related DNA damage in human somatic cells is not limited to the production of the full-length L1 mRNA because of the expression of the L1 splice transcript that likely contributes to the translation of the L1 ORF2 protein. | [] | We provide experimental support that L1-related DNA damage in human somatic cells is not limited to the production of the full-length L1 mRNA because of the expression of the L1 splice transcript that likely contributes to the translation of the L1 ORF2 protein. | true | true | true | true | true | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | The SpORF2 transcript is detected in numerous human tissues and the expression of SpORF2 mRNA exhibits tissues-specific variation. | [
"14",
"15",
"30",
"23"
] | 130 | 37,501 | 0 | false | The SpORF2 transcript is detected in numerous human tissues and the expression of SpORF2 mRNA exhibits tissues-specific variation. | [] | The SpORF2 transcript is detected in numerous human tissues and the expression of SpORF2 mRNA exhibits tissues-specific variation. | true | true | true | true | true | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | We also demonstrate that transient expression of the wt L1 or the splice SpORF2 product in normal human fibroblasts and adult stem cells leads to a senescence-like phenotype. | [
"14",
"15",
"30",
"23"
] | 174 | 37,502 | 0 | false | We also demonstrate that transient expression of the wt L1 or the splice SpORF2 product in normal human fibroblasts and adult stem cells leads to a senescence-like phenotype. | [] | We also demonstrate that transient expression of the wt L1 or the splice SpORF2 product in normal human fibroblasts and adult stem cells leads to a senescence-like phenotype. | true | true | true | true | true | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Because L1 activity has been well established to contribute to germ line mutagenesis | [
"14",
"15",
"30",
"23"
] | 84 | 37,503 | 0 | false | Because L1 activity has been well established to contribute to germ line mutagenesis | [] | Because L1 activity has been well established to contribute to germ line mutagenesis | true | true | false | true | false | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | [reviewed in ref. | [
"14",
"15",
"30",
"23"
] | 17 | 37,504 | 0 | false | [reviewed in ref. | [] | [reviewed in ref. | false | false | true | true | false | 6,423 |
4 | INTRODUCTION | 1 | 23 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | (23)], our finding of somatic L1 expression in a number of human tissues suggests that L1 elements need to be considered as an endogenous mutagen not only in germ line but also in somatic tissues for humans. | [
"14",
"15",
"30",
"23"
] | 207 | 37,505 | 1 | false | ], our finding of somatic L1 expression in a number of human tissues suggests that L1 elements need to be considered as an endogenous mutagen not only in germ line but also in somatic tissues for humans. | [
"23"
] | ], our finding of somatic L1 expression in a number of human tissues suggests that L1 elements need to be considered as an endogenous mutagen not only in germ line but also in somatic tissues for humans. | false | false | true | true | false | 6,423 |
4 | INTRODUCTION | 1 | 14 | [
"B14",
"B15",
"B30",
"B23"
] | 20,215,437 | pmid-16554555|pmid-14625551|pmid-18261861|pmid-18256243|pmid-16670018|pmid-16507671|pmid-16490214|pmid-16490214|pmid-16554555|pmid-18381897|pmid-17028956|pmid-17157332|pmid-16490214|pmid-8945517|pmid-12897783|pmid-16670018|pmid-15888314|pmid-17202845|pmid-1952798|pmid-3453778 | Our findings suggest that even low levels of somatic DNA damage due to L1 activity have the potential to contribute to genetic instability, aging, and age-related diseases, such as cancer. | [
"14",
"15",
"30",
"23"
] | 188 | 37,506 | 0 | false | Our findings suggest that even low levels of somatic DNA damage due to L1 activity have the potential to contribute to genetic instability, aging, and age-related diseases, such as cancer. | [] | Our findings suggest that even low levels of somatic DNA damage due to L1 activity have the potential to contribute to genetic instability, aging, and age-related diseases, such as cancer. | true | true | true | true | true | 6,423 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | The field of human mobile elements has often focused on their mutagenic effect within the germ line (5,6) because transposable element amplification to high copy number in the genome is dependent on germ line insertions. | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 220 | 37,507 | 0 | false | The field of human mobile elements has often focused on their mutagenic effect within the germ line because transposable element amplification to high copy number in the genome is dependent on germ line insertions. | [
"5,6"
] | The field of human mobile elements has often focused on their mutagenic effect within the germ line because transposable element amplification to high copy number in the genome is dependent on germ line insertions. | true | true | true | true | true | 6,424 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | Detection of endogenous FL or SpORF2 L1 transcripts in this study in many tested adult tissues broadens the potential impact of mobile elements on human health and development. | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 176 | 37,508 | 0 | false | Detection of endogenous FL or SpORF2 L1 transcripts in this study in many tested adult tissues broadens the potential impact of mobile elements on human health and development. | [] | Detection of endogenous FL or SpORF2 L1 transcripts in this study in many tested adult tissues broadens the potential impact of mobile elements on human health and development. | true | true | true | true | true | 6,424 |
0 | DISCUSSION | 1 | 8 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | Our findings of modest levels of the FL L1 expression in human ovary and testis, and expression of only processed L1 mRNAs in kidney, lung, liver and brain are in agreement with the reported expression in a transgenic mouse model (8). | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 234 | 37,509 | 1 | false | Our findings of modest levels of the FL L1 expression in human ovary and testis, and expression of only processed L1 mRNAs in kidney, lung, liver and brain are in agreement with the reported expression in a transgenic mouse model. | [
"8"
] | Our findings of modest levels of the FL L1 expression in human ovary and testis, and expression of only processed L1 mRNAs in kidney, lung, liver and brain are in agreement with the reported expression in a transgenic mouse model. | true | true | true | true | true | 6,424 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | However, sporadic tissues, such as esophagus, placenta and prostate demonstrate that some somatic tissues can express L1 elements fairly well. | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 142 | 37,510 | 0 | false | However, sporadic tissues, such as esophagus, placenta and prostate demonstrate that some somatic tissues can express L1 elements fairly well. | [] | However, sporadic tissues, such as esophagus, placenta and prostate demonstrate that some somatic tissues can express L1 elements fairly well. | true | true | true | true | true | 6,424 |
0 | DISCUSSION | 1 | 21 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | A recent report of L1 mobilization in a transgenic mouse model demonstrates higher L1 retrotransposition rates in somatic tissues than in the germ line (21), suggesting the possibility that expression of endogenous L1 elements in differentiated tissues may result in an appreciable amount of damage over time. | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 309 | 37,511 | 1 | false | A recent report of L1 mobilization in a transgenic mouse model demonstrates higher L1 retrotransposition rates in somatic tissues than in the germ line, suggesting the possibility that expression of endogenous L1 elements in differentiated tissues may result in an appreciable amount of damage over time. | [
"21"
] | A recent report of L1 mobilization in a transgenic mouse model demonstrates higher L1 retrotransposition rates in somatic tissues than in the germ line, suggesting the possibility that expression of endogenous L1 elements in differentiated tissues may result in an appreciable amount of damage over time. | true | true | true | true | true | 6,424 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | Although FL L1 mRNAs are certainly the dominant source of L1 retrotransposition, generation of the SpORF2 transcript that can make functional ORF2 protein indicates that the FL L1 transcripts with both functional ORFs are not absolutely required to cause cellular damage. | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 271 | 37,512 | 0 | false | Although FL L1 mRNAs are certainly the dominant source of L1 retrotransposition, generation of the SpORF2 transcript that can make functional ORF2 protein indicates that the FL L1 transcripts with both functional ORFs are not absolutely required to cause cellular damage. | [] | Although FL L1 mRNAs are certainly the dominant source of L1 retrotransposition, generation of the SpORF2 transcript that can make functional ORF2 protein indicates that the FL L1 transcripts with both functional ORFs are not absolutely required to cause cellular damage. | true | true | true | true | true | 6,424 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | This contrasts with previous assumptions that functional ORF2 protein can only be produced from the FL mRNAs (37,38). | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 117 | 37,513 | 0 | false | This contrasts with previous assumptions that functional ORF2 protein can only be produced from the FL mRNAs. | [
"37,38"
] | This contrasts with previous assumptions that functional ORF2 protein can only be produced from the FL mRNAs. | true | true | true | true | true | 6,424 |
0 | DISCUSSION | 1 | 5 | [
"B5",
"B6",
"B8",
"B21",
"B37",
"B38"
] | 20,215,437 | pmid-1662412|pmid-11237011|pmid-11237011|pmid-15608246|pmid-8945518|pmid-8139560|pmid-7878012|pmid-12415270|pmid-18615728|pmid-16418485|pmid-8265584 | It is apparent that detection of the L1 ORF2 protein does not necessarily guarantee the presence of the full-length L1 mRNA. | [
"5",
"6",
"8",
"21",
"37",
"38"
] | 124 | 37,514 | 0 | false | It is apparent that detection of the L1 ORF2 protein does not necessarily guarantee the presence of the full-length L1 mRNA. | [] | It is apparent that detection of the L1 ORF2 protein does not necessarily guarantee the presence of the full-length L1 mRNA. | true | true | true | true | true | 6,424 |
1 | DISCUSSION | 1 | 22 | [
"B22",
"B51",
"B52",
"B22"
] | 20,215,437 | pmid-8139560|pmid-7878012|pmid-15056671|pmid-12415270|pmid-17145770|pmid-2454389|pmid-15056671|pmid-15959507|pmid-19772661|pmid-19657334|pmid-16554555|pmid-14625551|pmid-1310068|pmid-16698926|pmid-17145770|pmid-15959507|pmid-17124176|pmid-16365384|pmid-18615728|pmid-12897783|pmid-14628287|pmid-10742098|pmid-12897783 | Insertion of L1 elements is not the only mechanism by which they may damage genomes. | [
"22",
"51",
"52",
"22"
] | 84 | 37,515 | 0 | false | Insertion of L1 elements is not the only mechanism by which they may damage genomes. | [] | Insertion of L1 elements is not the only mechanism by which they may damage genomes. | true | true | true | true | true | 6,425 |
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