paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3 | DISCUSSION | 1 | 73 | [
"bib73",
"bib24",
"bib74",
"bib77"
] | 20,179,319 | NA|pmid-17573352|pmid-11292382|pmid-3922757 | The spontaneous transfer of ceramide may be significant as it is unclear whether ceramides are completely degraded by acid ceramidase or, in part, can leave the acidic compartments intact as shown previously for endocytosed, nondegradable analogs of glucosylceramide and gangliosides GM2 and GM1 (74–77). | [
"73",
"24",
"74",
"77"
] | 304 | 38,916 | 0 | false | The spontaneous transfer of ceramide may be significant as it is unclear whether ceramides are completely degraded by acid ceramidase or, in part, can leave the acidic compartments intact as shown previously for endocytosed, nondegradable analogs of glucosylceramide and gangliosides GM2 and GM1. | [
"74–77"
] | The spontaneous transfer of ceramide may be significant as it is unclear whether ceramides are completely degraded by acid ceramidase or, in part, can leave the acidic compartments intact as shown previously for endocytosed, nondegradable analogs of glucosylceramide and gangliosides GM2 and GM1. | true | true | true | true | true | 6,699 |
4 | DISCUSSION | 1 | 54 | [
"bib54",
"bib35",
"bib29"
] | 20,179,319 | pmid-11104761|pmid-8204660|pmid-17552909 | Ceramides are degraded at pH values below 4.8 by acid ceramidase into fatty acids and sphingoid bases, the final products of sphingolipid degradation in the lysosomes (54). | [
"54",
"35",
"29"
] | 172 | 38,917 | 1 | false | Ceramides are degraded at pH values below 4.8 by acid ceramidase into fatty acids and sphingoid bases, the final products of sphingolipid degradation in the lysosomes. | [
"54"
] | Ceramides are degraded at pH values below 4.8 by acid ceramidase into fatty acids and sphingoid bases, the final products of sphingolipid degradation in the lysosomes. | true | true | true | true | true | 6,700 |
4 | DISCUSSION | 1 | 54 | [
"bib54",
"bib35",
"bib29"
] | 20,179,319 | pmid-11104761|pmid-8204660|pmid-17552909 | Our data show that oleic acid, linoleic acid, sphinganine, and sphingosine are spontaneously transferred, even within a short experimental period of 3 min. | [
"54",
"35",
"29"
] | 155 | 38,918 | 0 | false | Our data show that oleic acid, linoleic acid, sphinganine, and sphingosine are spontaneously transferred, even within a short experimental period of 3 min. | [] | Our data show that oleic acid, linoleic acid, sphinganine, and sphingosine are spontaneously transferred, even within a short experimental period of 3 min. | true | true | true | true | true | 6,700 |
4 | DISCUSSION | 1 | 35 | [
"bib54",
"bib35",
"bib29"
] | 20,179,319 | pmid-11104761|pmid-8204660|pmid-17552909 | Their abnormally high levels in the liver, spleen, and cerebral cortex of patients with NPC disease and other lysosomal disorders previously reported (35) does not seem to be due to lack of NPC2. | [
"54",
"35",
"29"
] | 195 | 38,919 | 1 | false | Their abnormally high levels in the liver, spleen, and cerebral cortex of patients with NPC disease and other lysosomal disorders previously reported does not seem to be due to lack of NPC2. | [
"35"
] | Their abnormally high levels in the liver, spleen, and cerebral cortex of patients with NPC disease and other lysosomal disorders previously reported does not seem to be due to lack of NPC2. | true | true | true | true | true | 6,700 |
4 | DISCUSSION | 1 | 29 | [
"bib54",
"bib35",
"bib29"
] | 20,179,319 | pmid-11104761|pmid-8204660|pmid-17552909 | With our improved assay conditions, we could clearly demonstrate that, in contrast to NPC2, other lysosomal proteins (GM2AP, Sap C, and others) do not mediate cholesterol transfer at substantial rates, although a slightly faster transfer rate was reported recently (29). | [
"54",
"35",
"29"
] | 270 | 38,920 | 1 | false | With our improved assay conditions, we could clearly demonstrate that, in contrast to NPC2, other lysosomal proteins (GM2AP, Sap C, and others) do not mediate cholesterol transfer at substantial rates, although a slightly faster transfer rate was reported recently. | [
"29"
] | With our improved assay conditions, we could clearly demonstrate that, in contrast to NPC2, other lysosomal proteins do not mediate cholesterol transfer at substantial rates, although a slightly faster transfer rate was reported recently. | true | true | true | true | true | 6,700 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | BMP (C18:1) has been reported to enhance degradation of sphingolipids and glycosphingolipids by lysosomal exohydrolases in the presence of sphingolipid activator proteins (39, 54, 58, 59). | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 188 | 38,921 | 0 | false | BMP (C18:1) has been reported to enhance degradation of sphingolipids and glycosphingolipids by lysosomal exohydrolases in the presence of sphingolipid activator proteins. | [
"39, 54, 58, 59"
] | BMP (C18:1) has been reported to enhance degradation of sphingolipids and glycosphingolipids by lysosomal exohydrolases in the presence of sphingolipid activator proteins. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 29 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | Its ability to stimulate cholesterol transfer at lysosomal pH has been previously reported (29). | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 96 | 38,922 | 1 | false | Its ability to stimulate cholesterol transfer at lysosomal pH has been previously reported. | [
"29"
] | Its ability to stimulate cholesterol transfer at lysosomal pH has been previously reported. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 29 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | 4A clearly shows that BMP also stimulates cholesterol transfer at the pH of the late endosomal compartments (around pH 5.0), although to a lesser extent than that previously reported at lysosomal pH of around 4.5 (29). | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 218 | 38,923 | 1 | false | 4A clearly shows that BMP also stimulates cholesterol transfer at the pH of the late endosomal compartments (around pH 5.0), although to a lesser extent than that previously reported at lysosomal pH of around 4.5. | [
"29"
] | 4A clearly shows that BMP also stimulates cholesterol transfer at the pH of the late endosomal compartments (around pH 5.0), although to a lesser extent than that previously reported at lysosomal pH of around 4.5. | false | false | true | true | false | 6,701 |
5 | DISCUSSION | 1 | 3 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | This result is reasonable because it confirms the observation that BMP concentration increases in the inner membranes of the endocytic pathway while cholesterol concentration and the luminal pH decreases (3). | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 208 | 38,924 | 1 | false | This result is reasonable because it confirms the observation that BMP concentration increases in the inner membranes of the endocytic pathway while cholesterol concentration and the luminal pH decreases. | [
"3"
] | This result is reasonable because it confirms the observation that BMP concentration increases in the inner membranes of the endocytic pathway while cholesterol concentration and the luminal pH decreases. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | However, at a 30% molar concentration of BMP, the rate of cholesterol transfer is more than doubled compared with the cholesterol transfer rate recorded in the absence of BMP at pH 5.0. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 185 | 38,925 | 0 | false | However, at a 30% molar concentration of BMP, the rate of cholesterol transfer is more than doubled compared with the cholesterol transfer rate recorded in the absence of BMP at pH 5.0. | [] | However, at a 30% molar concentration of BMP, the rate of cholesterol transfer is more than doubled compared with the cholesterol transfer rate recorded in the absence of BMP at pH 5.0. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | It is noteworthy that BMP (18:1) with native acyl chains stimulates cholesterol transfer much better than BMP (14:0) with unnatural acyl chains. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 144 | 38,926 | 0 | false | It is noteworthy that BMP (18:1) with native acyl chains stimulates cholesterol transfer much better than BMP (14:0) with unnatural acyl chains. | [] | It is noteworthy that BMP (18:1) with native acyl chains stimulates cholesterol transfer much better than BMP (14:0) with unnatural acyl chains. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | As BMP (18:1) and BMP (14:0) have the same configuration, their effect on cholesterol transport seems to be solely related to the acyl chain length and/or unsaturation. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 168 | 38,927 | 0 | false | As BMP (18:1) and BMP (14:0) have the same configuration, their effect on cholesterol transport seems to be solely related to the acyl chain length and/or unsaturation. | [] | As BMP (18:1) and BMP (14:0) have the same configuration, their effect on cholesterol transport seems to be solely related to the acyl chain length and/or unsaturation. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | It will be interesting to see what the effect of BMP (22:5) with longer acyl chains will be. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 92 | 38,928 | 0 | false | It will be interesting to see what the effect of BMP with longer acyl chains will be. | [
"22:5"
] | It will be interesting to see what the effect of BMP with longer acyl chains will be. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | There may also be a significant difference between the effects of natural BMPs and the synthetic ones used here. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 112 | 38,929 | 0 | false | There may also be a significant difference between the effects of natural BMPs and the synthetic ones used here. | [] | There may also be a significant difference between the effects of natural BMPs and the synthetic ones used here. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | It is obvious from this work and the previous reports (22, 29, 30) that BMP is needed to stimulate cholesterol transfer. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 120 | 38,930 | 0 | false | It is obvious from this work and the previous reports that BMP is needed to stimulate cholesterol transfer. | [
"22, 29, 30"
] | It is obvious from this work and the previous reports that BMP is needed to stimulate cholesterol transfer. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 39 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | The combined presence of BMP and hydrolytic enzymes (e.g., acid sphingomyelinase) might have an important effect on cholesterol transfer. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 137 | 38,931 | 0 | false | The combined presence of BMP and hydrolytic enzymes (e.g., acid sphingomyelinase) might have an important effect on cholesterol transfer. | [] | The combined presence of BMP and hydrolytic enzymes (e.g., acid sphingomyelinase) might have an important effect on cholesterol transfer. | true | true | true | true | true | 6,701 |
5 | DISCUSSION | 1 | 78 | [
"bib39",
"bib54",
"bib58",
"bib59",
"bib29",
"bib29",
"bib3",
"bib22",
"bib29",
"bib30",
"bib78"
] | 20,179,319 | pmid-11308026|pmid-11104761|pmid-11278374|pmid-10942779|pmid-17552909|pmid-17552909|pmid-12694561|pmid-18823126|pmid-17552909|pmid-16606609|NA | For instance, exogenously added sphingomeylinase reduced accumulation of both SM and cholesterol in cultured fibroblasts of NPC patients (78), which supports the notion above. | [
"39",
"54",
"58",
"59",
"29",
"29",
"3",
"22",
"29",
"30",
"78"
] | 175 | 38,932 | 1 | false | For instance, exogenously added sphingomeylinase reduced accumulation of both SM and cholesterol in cultured fibroblasts of NPC patients, which supports the notion above. | [
"78"
] | For instance, exogenously added sphingomeylinase reduced accumulation of both SM and cholesterol in cultured fibroblasts of NPC patients, which supports the notion above. | true | true | true | true | true | 6,701 |
6 | DISCUSSION | 1 | 79 | [
"bib79",
"bib60",
"bib61",
"bib40",
"bib41",
"bib42",
"bib43",
"bib29"
] | 20,179,319 | NA|pmid-3390137|pmid-2790049|pmid-16920840|pmid-1868053|pmid-9891780|pmid-9177342|pmid-17552909 | The high accumulation of cholesterol in SM storage diseases, such as Niemann-Pick disease type A and B, has been reported to be secondary to SM accumulation (79). | [
"79",
"60",
"61",
"40",
"41",
"42",
"43",
"29"
] | 162 | 38,933 | 1 | false | The high accumulation of cholesterol in SM storage diseases, such as Niemann-Pick disease type A and B, has been reported to be secondary to SM accumulation. | [
"79"
] | The high accumulation of cholesterol in SM storage diseases, such as Niemann-Pick disease type A and B, has been reported to be secondary to SM accumulation. | true | true | true | true | true | 6,702 |
6 | DISCUSSION | 1 | 79 | [
"bib79",
"bib60",
"bib61",
"bib40",
"bib41",
"bib42",
"bib43",
"bib29"
] | 20,179,319 | NA|pmid-3390137|pmid-2790049|pmid-16920840|pmid-1868053|pmid-9891780|pmid-9177342|pmid-17552909 | As seen in Fig. | [
"79",
"60",
"61",
"40",
"41",
"42",
"43",
"29"
] | 15 | 38,934 | 0 | false | As seen in Fig. | [] | As seen in Fig. | true | true | true | true | true | 6,702 |
6 | DISCUSSION | 1 | 79 | [
"bib79",
"bib60",
"bib61",
"bib40",
"bib41",
"bib42",
"bib43",
"bib29"
] | 20,179,319 | NA|pmid-3390137|pmid-2790049|pmid-16920840|pmid-1868053|pmid-9891780|pmid-9177342|pmid-17552909 | 5A, the inclusion of increasing amounts of SM into the vesicles inhibited cholesterol transfer nearly completely. | [
"79",
"60",
"61",
"40",
"41",
"42",
"43",
"29"
] | 113 | 38,935 | 0 | false | 5A, the inclusion of increasing amounts of SM into the vesicles inhibited cholesterol transfer nearly completely. | [] | 5A, the inclusion of increasing amounts of SM into the vesicles inhibited cholesterol transfer nearly completely. | false | false | true | true | false | 6,702 |
6 | DISCUSSION | 1 | 79 | [
"bib79",
"bib60",
"bib61",
"bib40",
"bib41",
"bib42",
"bib43",
"bib29"
] | 20,179,319 | NA|pmid-3390137|pmid-2790049|pmid-16920840|pmid-1868053|pmid-9891780|pmid-9177342|pmid-17552909 | This finding is attributed to the high affinity of cholesterol to SM-rich membranes (60, 61). | [
"79",
"60",
"61",
"40",
"41",
"42",
"43",
"29"
] | 93 | 38,936 | 0 | false | This finding is attributed to the high affinity of cholesterol to SM-rich membranes. | [
"60, 61"
] | This finding is attributed to the high affinity of cholesterol to SM-rich membranes. | true | true | true | true | true | 6,702 |
6 | DISCUSSION | 1 | 79 | [
"bib79",
"bib60",
"bib61",
"bib40",
"bib41",
"bib42",
"bib43",
"bib29"
] | 20,179,319 | NA|pmid-3390137|pmid-2790049|pmid-16920840|pmid-1868053|pmid-9891780|pmid-9177342|pmid-17552909 | SM interacts with cholesterol by forming hydrogen bonds between the OH-group of cholesterol and the amide group of SM (40, 41), thereby keeping cholesterol in the membrane (42, 43). | [
"79",
"60",
"61",
"40",
"41",
"42",
"43",
"29"
] | 181 | 38,937 | 0 | false | SM interacts with cholesterol by forming hydrogen bonds between the OH-group of cholesterol and the amide group of SM, thereby keeping cholesterol in the membrane. | [
"40, 41",
"42, 43"
] | SM interacts with cholesterol by forming hydrogen bonds between the OH-group of cholesterol and the amide group of SM, thereby keeping cholesterol in the membrane. | true | true | true | true | true | 6,702 |
6 | DISCUSSION | 1 | 29 | [
"bib79",
"bib60",
"bib61",
"bib40",
"bib41",
"bib42",
"bib43",
"bib29"
] | 20,179,319 | NA|pmid-3390137|pmid-2790049|pmid-16920840|pmid-1868053|pmid-9891780|pmid-9177342|pmid-17552909 | The inhibitory activity of SM on cholesterol transfer by NPC2 is more pronounced at pH 5.0 than at pH 4.2 (29). | [
"79",
"60",
"61",
"40",
"41",
"42",
"43",
"29"
] | 111 | 38,938 | 1 | false | The inhibitory activity of SM on cholesterol transfer by NPC2 is more pronounced at pH 5.0 than at pH 4.2. | [
"29"
] | The inhibitory activity of SM on cholesterol transfer by NPC2 is more pronounced at pH 5.0 than at pH 4.2. | true | true | true | true | true | 6,702 |
7 | DISCUSSION | 1 | 39 | [
"bib39",
"bib80",
"bib44",
"bib62",
"bib63"
] | 20,179,319 | pmid-11308026|pmid-20111001|pmid-14699154|pmid-16129675|pmid-16126159 | At an optimum pH of 5.5 (39) membrane-stabilizing SM may be degraded to ceramide efficiently by acid sphingomyelinase in the intraendosomal membranes of late endosomes (Fig. | [
"39",
"80",
"44",
"62",
"63"
] | 173 | 38,939 | 1 | false | At an optimum pH of 5.5 membrane-stabilizing SM may be degraded to ceramide efficiently by acid sphingomyelinase in the intraendosomal membranes of late endosomes (Fig. | [
"39"
] | At an optimum pH of 5.5 membrane-stabilizing SM may be degraded to ceramide efficiently by acid sphingomyelinase in the intraendosomal membranes of late endosomes (Fig. | true | true | true | true | true | 6,703 |
7 | DISCUSSION | 1 | 39 | [
"bib39",
"bib80",
"bib44",
"bib62",
"bib63"
] | 20,179,319 | pmid-11308026|pmid-20111001|pmid-14699154|pmid-16129675|pmid-16126159 | This may stimulate the transport of cholesterol within late endosomes. | [
"39",
"80",
"44",
"62",
"63"
] | 70 | 38,940 | 0 | false | This may stimulate the transport of cholesterol within late endosomes. | [] | This may stimulate the transport of cholesterol within late endosomes. | true | true | true | true | true | 6,703 |
7 | DISCUSSION | 1 | 39 | [
"bib39",
"bib80",
"bib44",
"bib62",
"bib63"
] | 20,179,319 | pmid-11308026|pmid-20111001|pmid-14699154|pmid-16129675|pmid-16126159 | Indeed, as illustrated in Fig. | [
"39",
"80",
"44",
"62",
"63"
] | 30 | 38,941 | 0 | false | Indeed, as illustrated in Fig. | [] | Indeed, as illustrated in Fig. | true | true | true | true | true | 6,703 |
7 | DISCUSSION | 1 | 39 | [
"bib39",
"bib80",
"bib44",
"bib62",
"bib63"
] | 20,179,319 | pmid-11308026|pmid-20111001|pmid-14699154|pmid-16129675|pmid-16126159 | 5B, removal of SM greatly stimulated cholesterol transfer in the presence of BMP (arrow). | [
"39",
"80",
"44",
"62",
"63"
] | 89 | 38,942 | 0 | false | 5B, removal of SM greatly stimulated cholesterol transfer in the presence of BMP (arrow). | [] | 5B, removal of SM greatly stimulated cholesterol transfer in the presence of BMP (arrow). | false | false | true | true | false | 6,703 |
7 | DISCUSSION | 1 | 39 | [
"bib39",
"bib80",
"bib44",
"bib62",
"bib63"
] | 20,179,319 | pmid-11308026|pmid-20111001|pmid-14699154|pmid-16129675|pmid-16126159 | This shows the important function of acid sphingomyelinase in preventing lipid traffic jam in the presence of BMP in the late endosomal compartments. | [
"39",
"80",
"44",
"62",
"63"
] | 149 | 38,943 | 0 | false | This shows the important function of acid sphingomyelinase in preventing lipid traffic jam in the presence of BMP in the late endosomal compartments. | [] | This shows the important function of acid sphingomyelinase in preventing lipid traffic jam in the presence of BMP in the late endosomal compartments. | true | true | true | true | true | 6,703 |
7 | DISCUSSION | 1 | 80 | [
"bib39",
"bib80",
"bib44",
"bib62",
"bib63"
] | 20,179,319 | pmid-11308026|pmid-20111001|pmid-14699154|pmid-16129675|pmid-16126159 | This is also corroborated by the observation that Hsp 70 stimulates the activity of acid sphingomeylinase and thus the degradation of SM (80). | [
"39",
"80",
"44",
"62",
"63"
] | 142 | 38,944 | 1 | false | This is also corroborated by the observation that Hsp 70 stimulates the activity of acid sphingomeylinase and thus the degradation of SM. | [
"80"
] | This is also corroborated by the observation that Hsp 70 stimulates the activity of acid sphingomeylinase and thus the degradation of SM. | true | true | true | true | true | 6,703 |
7 | DISCUSSION | 1 | 39 | [
"bib39",
"bib80",
"bib44",
"bib62",
"bib63"
] | 20,179,319 | pmid-11308026|pmid-20111001|pmid-14699154|pmid-16129675|pmid-16126159 | The generation of ceramide in the presence of BMP facilitates the exit of cholesterol from late endosomal compartments, by acting as a cholesterol-competitor, thereby displacing cholesterol from the bilayers (44, 62, 63). | [
"39",
"80",
"44",
"62",
"63"
] | 221 | 38,945 | 0 | false | The generation of ceramide in the presence of BMP facilitates the exit of cholesterol from late endosomal compartments, by acting as a cholesterol-competitor, thereby displacing cholesterol from the bilayers. | [
"44, 62, 63"
] | The generation of ceramide in the presence of BMP facilitates the exit of cholesterol from late endosomal compartments, by acting as a cholesterol-competitor, thereby displacing cholesterol from the bilayers. | true | true | true | true | true | 6,703 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | The reported loss of fluorescence in our earlier transfer assay (29) was thought to have arisen from either i) the transfer or quenching of the fluorescence probe NBD-PE or the possibility of liposome adherence to the wall of the reaction vessel; or ii) the fusion of the donor and acceptor vesicles. | [
"29"
] | 300 | 38,946 | 1 | false | The reported loss of fluorescence in our earlier transfer assay was thought to have arisen from either i) the transfer or quenching of the fluorescence probe NBD-PE or the possibility of liposome adherence to the wall of the reaction vessel; or ii) the fusion of the donor and acceptor vesicles. | [
"29"
] | The reported loss of fluorescence in our earlier transfer assay was thought to have arisen from either i) the transfer or quenching of the fluorescence probe NBD-PE or the possibility of liposome adherence to the wall of the reaction vessel; or ii) the fusion of the donor and acceptor vesicles. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | We made a significant change in our transfer assay to assess the source of the loss of fluorescence by using a donor-to-acceptor liposome ratio of 1:1. | [
"29"
] | 151 | 38,947 | 0 | false | We made a significant change in our transfer assay to assess the source of the loss of fluorescence by using a donor-to-acceptor liposome ratio of 1:1. | [] | We made a significant change in our transfer assay to assess the source of the loss of fluorescence by using a donor-to-acceptor liposome ratio of 1:1. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | Assuming an even distribution of NBD-PE in liposomes, a significant extent of fluorescence self-quenching at 4 mol% is not very likely. | [
"29"
] | 135 | 38,948 | 0 | false | Assuming an even distribution of NBD-PE in liposomes, a significant extent of fluorescence self-quenching at 4 mol% is not very likely. | [] | Assuming an even distribution of NBD-PE in liposomes, a significant extent of fluorescence self-quenching at 4 mol% is not very likely. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | Also the inverse experiment (fluorescence NBD-PE in the donor vesicles and radiolabeled PC in the acceptor liposomes) leads to the same loss of radioactivity as previously of fluorescence, which again argues against self-quenching and a reduction of the NBD group. | [
"29"
] | 264 | 38,949 | 0 | false | Also the inverse experiment (fluorescence NBD-PE in the donor vesicles and radiolabeled PC in the acceptor liposomes) leads to the same loss of radioactivity as previously of fluorescence, which again argues against self-quenching and a reduction of the NBD group. | [] | Also the inverse experiment (fluorescence NBD-PE in the donor vesicles and radiolabeled PC in the acceptor liposomes) leads to the same loss of radioactivity as previously of fluorescence, which again argues against self-quenching and a reduction of the NBD group. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | We also checked the possibility of liposome adherence to the wall of the reaction vessel. | [
"29"
] | 89 | 38,950 | 0 | false | We also checked the possibility of liposome adherence to the wall of the reaction vessel. | [] | We also checked the possibility of liposome adherence to the wall of the reaction vessel. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | For this we used the inverse experiment and measured radioactivity in the absence and presence of NPC2 remaining in the assay volume. | [
"29"
] | 133 | 38,951 | 0 | false | For this we used the inverse experiment and measured radioactivity in the absence and presence of NPC2 remaining in the assay volume. | [] | For this we used the inverse experiment and measured radioactivity in the absence and presence of NPC2 remaining in the assay volume. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | The loss of radioactivity observed after 10 min, the incubation time in transfer/fusion assays, was less than 3% of the total radioactivity applied and was within the error of measurement. | [
"29"
] | 188 | 38,952 | 0 | false | The loss of radioactivity observed after 10 min, the incubation time in transfer/fusion assays, was less than 3% of the total radioactivity applied and was within the error of measurement. | [] | The loss of radioactivity observed after 10 min, the incubation time in transfer/fusion assays, was less than 3% of the total radioactivity applied and was within the error of measurement. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | We conclude, beyond any doubt, that the loss of fluorescence was due to membrane fusion. | [
"29"
] | 88 | 38,953 | 0 | false | We conclude, beyond any doubt, that the loss of fluorescence was due to membrane fusion. | [] | We conclude, beyond any doubt, that the loss of fluorescence was due to membrane fusion. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | However, in transfer experiments at pH 5.0 using a 1:5 ratio of donor-to-acceptor liposomes (Figs. | [
"29"
] | 98 | 38,954 | 0 | false | However, in transfer experiments at pH 5.0 using a 1:5 ratio of donor-to-acceptor liposomes (Figs. | [] | However, in transfer experiments at pH 5.0 using a 1:5 ratio of donor-to-acceptor liposomes (Figs. | true | true | true | true | true | 6,704 |
8 | DISCUSSION | 1 | 29 | [
"bib29"
] | 20,179,319 | pmid-17552909 | 2–6), the rate of fusion did not exceed 1%–3% and 5%–9% of the transfer rate after 10 min in the absence or presence of BMP, respectively. | [
"29"
] | 138 | 38,955 | 0 | false | 2–6), the rate of fusion did not exceed 1%–3% and 5%–9% of the transfer rate after 10 min in the absence or presence of BMP, respectively. | [] | 2–6), the rate of fusion did not exceed 1%–3% and 5%–9% of the transfer rate after 10 min in the absence or presence of BMP, respectively. | false | false | true | true | false | 6,704 |
9 | DISCUSSION | 1 | 66 | [
"bib66",
"bib69",
"bib81",
"bib82"
] | 20,179,319 | pmid-15652344|pmid-9972880|pmid-15047193|pmid-16256068 | The extent to which bovine NPC2 and membrane lipids mediate membrane fusion was investigated using the newly designed fusion assay, which is based on the use of streptavidin-coated paramagnetic beads as described in “Materials and Methods.” | [
"66",
"69",
"81",
"82"
] | 240 | 38,956 | 0 | false | The extent to which bovine NPC2 and membrane lipids mediate membrane fusion was investigated using the newly designed fusion assay, which is based on the use of streptavidin-coated paramagnetic beads as described in “Materials and Methods.” | [] | The extent to which bovine NPC2 and membrane lipids mediate membrane fusion was investigated using the newly designed fusion assay, which is based on the use of streptavidin-coated paramagnetic beads as described in “Materials and Methods.” | true | true | false | true | false | 6,705 |
9 | DISCUSSION | 1 | 66 | [
"bib66",
"bib69",
"bib81",
"bib82"
] | 20,179,319 | pmid-15652344|pmid-9972880|pmid-15047193|pmid-16256068 | Owing to its fusogenic property, Sap C (66–69) was used as a control in our fusion assays. | [
"66",
"69",
"81",
"82"
] | 90 | 38,957 | 0 | false | Owing to its fusogenic property, Sap C was used as a control in our fusion assays. | [
"66–69"
] | Owing to its fusogenic property, Sap C was used as a control in our fusion assays. | true | true | true | true | true | 6,705 |
9 | DISCUSSION | 1 | 66 | [
"bib66",
"bib69",
"bib81",
"bib82"
] | 20,179,319 | pmid-15652344|pmid-9972880|pmid-15047193|pmid-16256068 | Our results showed (Fig. | [
"66",
"69",
"81",
"82"
] | 24 | 38,958 | 0 | false | Our results showed (Fig. | [] | Our results showed (Fig. | true | true | true | true | true | 6,705 |
9 | DISCUSSION | 1 | 66 | [
"bib66",
"bib69",
"bib81",
"bib82"
] | 20,179,319 | pmid-15652344|pmid-9972880|pmid-15047193|pmid-16256068 | 8B) that bNPC2 also catalyzes membrane fusion both in the absence and presence of BMP, although significantly less so than Sap C. The fusogenic property of Sap C has been attributed to the lysine residues, which are located at positions 13 and 17 of the amino acid sequence of the protein (81, 82), A similar mechanism m... | [
"66",
"69",
"81",
"82"
] | 456 | 38,959 | 0 | false | 8B) that bNPC2 also catalyzes membrane fusion both in the absence and presence of BMP, although significantly less so than Sap C. The fusogenic property of Sap C has been attributed to the lysine residues, which are located at positions 13 and 17 of the amino acid sequence of the protein, A similar mechanism may also b... | [
"81, 82"
] | 8B) that bNPC2 also catalyzes membrane fusion both in the absence and presence of BMP, although significantly less so than Sap C. The fusogenic property of Sap C has been attributed to the lysine residues, which are located at positions 13 and 17 of the amino acid sequence of the protein, A similar mechanism may also b... | false | false | true | true | false | 6,705 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 20,376,904 | pmid-11745277|NA|NA | Lactic acidosis is one of the metabolic acidoses with increased anion gap. | [
"1",
"2"
] | 74 | 38,960 | 0 | false | Lactic acidosis is one of the metabolic acidoses with increased anion gap. | [] | Lactic acidosis is one of the metabolic acidoses with increased anion gap. | true | true | true | true | true | 6,706 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 20,376,904 | pmid-11745277|NA|NA | Lactic acidosis is defined as pH ≤ 7.35 and plasma lactate concentration ≥ 5 meq/L.1 | [
"1",
"2"
] | 84 | 38,961 | 0 | false | Lactic acidosis is defined as pH ≤ 7.35 and plasma lactate concentration ≥ 5 meq/L.1 | [] | Lactic acidosis is defined as pH ≤ 7.35 and plasma lactate concentration ≥ 5 meq/L.1 | true | true | false | true | false | 6,706 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 20,376,904 | pmid-11745277|NA|NA | There are two types of lactic acidosis. | [
"1",
"2"
] | 39 | 38,962 | 0 | false | There are two types of lactic acidosis. | [] | There are two types of lactic acidosis. | true | true | true | true | true | 6,706 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 20,376,904 | pmid-11745277|NA|NA | Type B occurs in malignancy, diabetes mellitus, renal or hepatic failure, severe infection, and drugs, whereas type A is caused by apparent tissue ischemia, as in shock, severe anemia, mitochondrial enzyme defects, and inhibitors such as carbon monoxide and cyanide.2 Lactic acidosis is a rare and often overlooked condi... | [
"1",
"2"
] | 423 | 38,963 | 0 | false | Type B occurs in malignancy, diabetes mellitus, renal or hepatic failure, severe infection, and drugs, whereas type A is caused by apparent tissue ischemia, as in shock, severe anemia, mitochondrial enzyme defects, and inhibitors such as carbon monoxide and cyanide.2 Lactic acidosis is a rare and often overlooked condi... | [] | Type B occurs in malignancy, diabetes mellitus, renal or hepatic failure, severe infection, and drugs, whereas type A is caused by apparent tissue ischemia, as in shock, severe anemia, mitochondrial enzyme defects, and inhibitors such as carbon monoxide and cyanide.2 Lactic acidosis is a rare and often overlooked condi... | true | true | true | true | true | 6,706 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 20,376,904 | pmid-11745277|NA|NA | We report a case of a 39-year-old man with recurred leukemia who presented with lactic acidosis. | [
"1",
"2"
] | 96 | 38,964 | 0 | false | We report a case of a 39-year-old man with recurred leukemia who presented with lactic acidosis. | [] | We report a case of a 39-year-old man with recurred leukemia who presented with lactic acidosis. | true | true | true | true | true | 6,706 |
0 | DISCUSSION | 1 | 3 | [
"B3"
] | 20,376,904 | pmid-11745277|NA|NA | Lactic acid is a degradation product of glucose in anaerobic conditions. | [
"3"
] | 72 | 38,965 | 0 | false | Lactic acid is a degradation product of glucose in anaerobic conditions. | [] | Lactic acid is a degradation product of glucose in anaerobic conditions. | true | true | true | true | true | 6,707 |
0 | DISCUSSION | 1 | 3 | [
"B3"
] | 20,376,904 | pmid-11745277|NA|NA | After glycolysis, pyruvate is converted to acetylcoenzyme A (CoA) to form energy in the Krebs cycle in aerobic conditions. | [
"3"
] | 122 | 38,966 | 0 | false | After glycolysis, pyruvate is converted to acetylcoenzyme A (CoA) to form energy in the Krebs cycle in aerobic conditions. | [] | After glycolysis, pyruvate is converted to acetylcoenzyme A (CoA) to form energy in the Krebs cycle in aerobic conditions. | true | true | true | true | true | 6,707 |
0 | DISCUSSION | 1 | 3 | [
"B3"
] | 20,376,904 | pmid-11745277|NA|NA | However, in anaerobic conditions, pyruvate is converted to lactate. | [
"3"
] | 67 | 38,967 | 0 | false | However, in anaerobic conditions, pyruvate is converted to lactate. | [] | However, in anaerobic conditions, pyruvate is converted to lactate. | true | true | true | true | true | 6,707 |
0 | DISCUSSION | 1 | 3 | [
"B3"
] | 20,376,904 | pmid-11745277|NA|NA | Lactate is normally formed in skeletal muscle, red blood cells, and the brain, and its amount is usually less than 1,500 mmol/day. | [
"3"
] | 130 | 38,968 | 0 | false | Lactate is normally formed in skeletal muscle, red blood cells, and the brain, and its amount is usually less than 1,500 mmol/day. | [] | Lactate is normally formed in skeletal muscle, red blood cells, and the brain, and its amount is usually less than 1,500 mmol/day. | true | true | true | true | true | 6,707 |
0 | DISCUSSION | 1 | 3 | [
"B3"
] | 20,376,904 | pmid-11745277|NA|NA | It is metabolized to form water and carbon dioxide in liver and kidneys. | [
"3"
] | 72 | 38,969 | 0 | false | It is metabolized to form water and carbon dioxide in liver and kidneys. | [] | It is metabolized to form water and carbon dioxide in liver and kidneys. | true | true | true | true | true | 6,707 |
0 | DISCUSSION | 1 | 3 | [
"B3"
] | 20,376,904 | pmid-11745277|NA|NA | Lactic acidosis results from an imbalance of formation and degradation of lactic acid.3 | [
"3"
] | 87 | 38,970 | 0 | false | Lactic acidosis results from an imbalance of formation and degradation of lactic acid.3 | [] | Lactic acidosis results from an imbalance of formation and degradation of lactic acid.3 | true | true | false | true | false | 6,707 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B5",
"B6"
] | 20,376,904 | pmid-14074652|NA|NA | More frequent causes of lactic acidosis in patients with malignancy are heart failure, sepsis, and decreased effective circulating volume, and these result in type A lactic acidosis. | [
"4",
"5",
"6"
] | 182 | 38,971 | 0 | false | More frequent causes of lactic acidosis in patients with malignancy are heart failure, sepsis, and decreased effective circulating volume, and these result in type A lactic acidosis. | [] | More frequent causes of lactic acidosis in patients with malignancy are heart failure, sepsis, and decreased effective circulating volume, and these result in type A lactic acidosis. | true | true | true | true | true | 6,708 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B5",
"B6"
] | 20,376,904 | pmid-14074652|NA|NA | Type B lactic acidosis in malignancy was first reported in 1963, in an acute leukemia patient.4 | [
"4",
"5",
"6"
] | 95 | 38,972 | 0 | false | Type B lactic acidosis in malignancy was first reported in 1963, in an acute leukemia patient.4 | [] | Type B lactic acidosis in malignancy was first reported in 1963, in an acute leukemia patient.4 | true | true | false | true | false | 6,708 |
1 | DISCUSSION | 1 | 4 | [
"B4",
"B5",
"B6"
] | 20,376,904 | pmid-14074652|NA|NA | In Korea, a case of lactic acidosis in a patient with leukemia transformed from lymphoma was reported in 1999,5 and a case of lactic acidosis due to thiamine deficiency was reported in 2007.6 | [
"4",
"5",
"6"
] | 191 | 38,973 | 0 | false | In Korea, a case of lactic acidosis in a patient with leukemia transformed from lymphoma was reported in 1999,5 and a case of lactic acidosis due to thiamine deficiency was reported in 2007.6 | [] | In Korea, a case of lactic acidosis in a patient with leukemia transformed from lymphoma was reported in 1999,5 and a case of lactic acidosis due to thiamine deficiency was reported in 2007.6 | true | true | false | true | false | 6,708 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B8",
"B10",
"B11"
] | 20,376,904 | pmid-17632264|pmid-17632264|pmid-4522886|pmid-4906508|pmid-11251027 | The present case did not have any signs of infection, hypoxia, or circulatory failure. | [
"7",
"7",
"8",
"10",
"11"
] | 86 | 38,974 | 0 | false | The present case did not have any signs of infection, hypoxia, or circulatory failure. | [] | The present case did not have any signs of infection, hypoxia, or circulatory failure. | true | true | true | true | true | 6,709 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B8",
"B10",
"B11"
] | 20,376,904 | pmid-17632264|pmid-17632264|pmid-4522886|pmid-4906508|pmid-11251027 | The mechanism of type B lactic acidosis in malignancy is unidentified, but it may be caused by tumor microembolism, increased glycolysis, and decreased gluconeogenesis by abnormal tumor metabolism, or decreased degradation of lactic acid because of extensive liver involvement. | [
"7",
"7",
"8",
"10",
"11"
] | 277 | 38,975 | 0 | false | The mechanism of type B lactic acidosis in malignancy is unidentified, but it may be caused by tumor microembolism, increased glycolysis, and decreased gluconeogenesis by abnormal tumor metabolism, or decreased degradation of lactic acid because of extensive liver involvement. | [] | The mechanism of type B lactic acidosis in malignancy is unidentified, but it may be caused by tumor microembolism, increased glycolysis, and decreased gluconeogenesis by abnormal tumor metabolism, or decreased degradation of lactic acid because of extensive liver involvement. | true | true | true | true | true | 6,709 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B8",
"B10",
"B11"
] | 20,376,904 | pmid-17632264|pmid-17632264|pmid-4522886|pmid-4906508|pmid-11251027 | Tumor necrosis factor-α is thought to play a role by reducing the activity of pyruvate dehydrogenase, which converts pyruvate to acetyl-CoA.7 | [
"7",
"7",
"8",
"10",
"11"
] | 141 | 38,976 | 0 | false | Tumor necrosis factor-α is thought to play a role by reducing the activity of pyruvate dehydrogenase, which converts pyruvate to acetyl-CoA.7 | [] | Tumor necrosis factor-α is thought to play a role by reducing the activity of pyruvate dehydrogenase, which converts pyruvate to acetyl-CoA.7 | true | true | false | true | false | 6,709 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B8",
"B10",
"B11"
] | 20,376,904 | pmid-17632264|pmid-17632264|pmid-4522886|pmid-4906508|pmid-11251027 | It also inhibits the cytochrome-dependent electron transport system and increases anaerobic glycolysis.7 | [
"7",
"7",
"8",
"10",
"11"
] | 104 | 38,977 | 0 | false | It also inhibits the cytochrome-dependent electron transport system and increases anaerobic glycolysis.7 | [] | It also inhibits the cytochrome-dependent electron transport system and increases anaerobic glycolysis.7 | true | true | false | true | false | 6,709 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B8",
"B10",
"B11"
] | 20,376,904 | pmid-17632264|pmid-17632264|pmid-4522886|pmid-4906508|pmid-11251027 | Lactic acid is metabolized mainly in the liver and kidneys. | [
"7",
"7",
"8",
"10",
"11"
] | 59 | 38,978 | 0 | false | Lactic acid is metabolized mainly in the liver and kidneys. | [] | Lactic acid is metabolized mainly in the liver and kidneys. | true | true | true | true | true | 6,709 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B8",
"B10",
"B11"
] | 20,376,904 | pmid-17632264|pmid-17632264|pmid-4522886|pmid-4906508|pmid-11251027 | The liver contributes to 90% of lactate metabolism and is frequently involved in patients with lactic acidosis.8-10 In the present case, there was no evidence of liver involvement. | [
"7",
"7",
"8",
"10",
"11"
] | 180 | 38,979 | 0 | false | The liver contributes to 90% of lactate metabolism and is frequently involved in patients with lactic acidosis.8-10 In the present case, there was no evidence of liver involvement. | [] | The liver contributes to 90% of lactate metabolism and is frequently involved in patients with lactic acidosis.8-10 In the present case, there was no evidence of liver involvement. | true | true | true | true | true | 6,709 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B8",
"B10",
"B11"
] | 20,376,904 | pmid-17632264|pmid-17632264|pmid-4522886|pmid-4906508|pmid-11251027 | Thiamine deficiency is also known to be a cause of lactic acidosis,11 but this patient was refractory to thiamine replacement. | [
"7",
"7",
"8",
"10",
"11"
] | 126 | 38,980 | 0 | false | Thiamine deficiency is also known to be a cause of lactic acidosis,11 but this patient was refractory to thiamine replacement. | [] | Thiamine deficiency is also known to be a cause of lactic acidosis,11 but this patient was refractory to thiamine replacement. | true | true | true | true | true | 6,709 |
3 | DISCUSSION | 1 | 1 | [
"B1",
"B1"
] | 20,376,904 | pmid-11745277|pmid-11745277 | Treatment of the primary condition, such as chemotherapy in malignancy, remains the mainstay of treatment.1 Treatment with renal replacement therapy is controversial. | [
"1",
"1"
] | 166 | 38,981 | 0 | false | Treatment of the primary condition, such as chemotherapy in malignancy, remains the mainstay of treatment.1 Treatment with renal replacement therapy is controversial. | [] | Treatment of the primary condition, such as chemotherapy in malignancy, remains the mainstay of treatment.1 Treatment with renal replacement therapy is controversial. | true | true | true | true | true | 6,710 |
3 | DISCUSSION | 1 | 1 | [
"B1",
"B1"
] | 20,376,904 | pmid-11745277|pmid-11745277 | In 2001, Sillos, et al.1 reported a case of lactic acidosis in an 11-year-old girl with acute lymphoblastic leukemia. | [
"1",
"1"
] | 117 | 38,982 | 0 | false | In 2001, Sillos, et al.1 reported a case of lactic acidosis in an 11-year-old girl with acute lymphoblastic leukemia. | [] | In 2001, Sillos, et al.1 reported a case of lactic acidosis in an 11-year-old girl with acute lymphoblastic leukemia. | true | true | true | true | true | 6,710 |
3 | DISCUSSION | 1 | 1 | [
"B1",
"B1"
] | 20,376,904 | pmid-11745277|pmid-11745277 | Blood pH improved rapidly after continuous veno-venous hemofiltration, but her plasma lactate concentration continued to increase. | [
"1",
"1"
] | 130 | 38,983 | 0 | false | Blood pH improved rapidly after continuous veno-venous hemofiltration, but her plasma lactate concentration continued to increase. | [] | Blood pH improved rapidly after continuous veno-venous hemofiltration, but her plasma lactate concentration continued to increase. | true | true | true | true | true | 6,710 |
3 | DISCUSSION | 1 | 1 | [
"B1",
"B1"
] | 20,376,904 | pmid-11745277|pmid-11745277 | It decreased after chemotherapy began to take effect. | [
"1",
"1"
] | 53 | 38,984 | 0 | false | It decreased after chemotherapy began to take effect. | [] | It decreased after chemotherapy began to take effect. | true | true | true | true | true | 6,710 |
4 | DISCUSSION | 0 | null | null | 20,376,904 | null | In patients with metabolic acidosis of unknown origin, lactic acidosis should be considered. | null | 92 | 38,985 | 0 | false | null | null | In patients with metabolic acidosis of unknown origin, lactic acidosis should be considered. | true | true | true | true | true | 6,711 |
4 | DISCUSSION | 0 | null | null | 20,376,904 | null | Serum lactic acid levels should be checked in cases of metabolic acidosis with increased anion gap. | null | 99 | 38,986 | 0 | false | null | null | Serum lactic acid levels should be checked in cases of metabolic acidosis with increased anion gap. | true | true | true | true | true | 6,711 |
4 | DISCUSSION | 0 | null | null | 20,376,904 | null | Leukemia usually presents as a fever, infection, and bleeding tendency, with lactic acidosis as a rare presentation. | null | 116 | 38,987 | 0 | false | null | null | Leukemia usually presents as a fever, infection, and bleeding tendency, with lactic acidosis as a rare presentation. | true | true | true | true | true | 6,711 |
4 | DISCUSSION | 0 | null | null | 20,376,904 | null | Physicians should be aware of lactic acidosis in recurring or advanced malignancy, and treatment of the underlying disease should be performed immediately. | null | 155 | 38,988 | 0 | false | null | null | Physicians should be aware of lactic acidosis in recurring or advanced malignancy, and treatment of the underlying disease should be performed immediately. | true | true | true | true | true | 6,711 |
0 | INTRODUCTION | 0 | null | null | 19,793,537 | null | Embryonated egg inoculation is commonly used to amplify avian RNA viruses. | null | 74 | 38,989 | 0 | false | null | null | Embryonated egg inoculation is commonly used to amplify avian RNA viruses. | true | true | true | true | true | 6,712 |
0 | INTRODUCTION | 0 | null | null | 19,793,537 | null | Successful viral replication mainly depends upon viral adaption to and replication in the cells of the embryonic and extraembryonic tissues. | null | 140 | 38,990 | 0 | false | null | null | Successful viral replication mainly depends upon viral adaption to and replication in the cells of the embryonic and extraembryonic tissues. | true | true | true | true | true | 6,712 |
0 | INTRODUCTION | 0 | null | null | 19,793,537 | null | Growth retardation and malformation of the embryo are the main indicators of viral reproduction in this system and signal the proper period for harvesting the amplified virions from the amniotic or chorioallantoic fluids. | null | 221 | 38,991 | 0 | false | null | null | Growth retardation and malformation of the embryo are the main indicators of viral reproduction in this system and signal the proper period for harvesting the amplified virions from the amniotic or chorioallantoic fluids. | true | true | true | true | true | 6,712 |
1 | INTRODUCTION | 1 | 5 | [
"R5",
"R6",
"R17",
"R31",
"R20",
"R26",
"R11",
"R19"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | The low efficiency of viral amplification may prevent etiology determinations, intensive surveillance of epidemiology and the tracing of potential natural domestic hosts for viral pathogens during an outbreak. | [
"5",
"6",
"17",
"31",
"20",
"26",
"11",
"19"
] | 209 | 38,992 | 0 | false | The low efficiency of viral amplification may prevent etiology determinations, intensive surveillance of epidemiology and the tracing of potential natural domestic hosts for viral pathogens during an outbreak. | [] | The low efficiency of viral amplification may prevent etiology determinations, intensive surveillance of epidemiology and the tracing of potential natural domestic hosts for viral pathogens during an outbreak. | true | true | true | true | true | 6,713 |
1 | INTRODUCTION | 1 | 5 | [
"R5",
"R6",
"R17",
"R31",
"R20",
"R26",
"R11",
"R19"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | For instance, avian metapneumovirus (MPV), which primarily attacks the respiratory tract, replicates inefficiently in embryonic eggs. | [
"5",
"6",
"17",
"31",
"20",
"26",
"11",
"19"
] | 133 | 38,993 | 0 | false | For instance, avian metapneumovirus (MPV), which primarily attacks the respiratory tract, replicates inefficiently in embryonic eggs. | [] | For instance, avian metapneumovirus (MPV), which primarily attacks the respiratory tract, replicates inefficiently in embryonic eggs. | true | true | true | true | true | 6,713 |
1 | INTRODUCTION | 1 | 5 | [
"R5",
"R6",
"R17",
"R31",
"R20",
"R26",
"R11",
"R19"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | Diagnosis of MPV infection is mainly dependent on the detection of viral RNA or viral antigens, but not viral isolation [5, 6]. | [
"5",
"6",
"17",
"31",
"20",
"26",
"11",
"19"
] | 127 | 38,994 | 0 | false | Diagnosis of MPV infection is mainly dependent on the detection of viral RNA or viral antigens, but not viral isolation. | [
"5, 6"
] | Diagnosis of MPV infection is mainly dependent on the detection of viral RNA or viral antigens, but not viral isolation. | true | true | true | true | true | 6,713 |
1 | INTRODUCTION | 1 | 5 | [
"R5",
"R6",
"R17",
"R31",
"R20",
"R26",
"R11",
"R19"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | In addition, to investigate the epidemiology of avian influenza viruses (AIV) requires efficient and sensitive viral detection and amplification system for comprehensive collection of the viruses from waterfowl and migratory birds [17, 31]. | [
"5",
"6",
"17",
"31",
"20",
"26",
"11",
"19"
] | 240 | 38,995 | 0 | false | In addition, to investigate the epidemiology of avian influenza viruses (AIV) requires efficient and sensitive viral detection and amplification system for comprehensive collection of the viruses from waterfowl and migratory birds. | [
"17, 31"
] | In addition, to investigate the epidemiology of avian influenza viruses (AIV) requires efficient and sensitive viral detection and amplification system for comprehensive collection of the viruses from waterfowl and migratory birds. | true | true | true | true | true | 6,713 |
1 | INTRODUCTION | 1 | 5 | [
"R5",
"R6",
"R17",
"R31",
"R20",
"R26",
"R11",
"R19"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | However, the wild-bird isolated AIV are usually mildly or non-pathogenic to chicken embryos [20, 26] and the efficiency of viral isolation is often unsatisfactory in embryonated eggs [11, 19]. | [
"5",
"6",
"17",
"31",
"20",
"26",
"11",
"19"
] | 192 | 38,996 | 0 | false | However, the wild-bird isolated AIV are usually mildly or non-pathogenic to chicken embryos and the efficiency of viral isolation is often unsatisfactory in embryonated eggs. | [
"20, 26",
"11, 19"
] | However, the wild-bird isolated AIV are usually mildly or non-pathogenic to chicken embryos and the efficiency of viral isolation is often unsatisfactory in embryonated eggs. | true | true | true | true | true | 6,713 |
2 | INTRODUCTION | 1 | 8 | [
"R8",
"R9",
"R15",
"R25",
"R7",
"R16",
"R24",
"R8",
"R15"
] | 19,793,537 | pmid-10366560|pmid-8116258|pmid-9060710|pmid-9101471|pmid-4565461|pmid-7609057|pmid-15332284|pmid-10366560|pmid-9060710|pmid-17296157|pmid-18483939|pmid-18645889|pmid-2545316|pmid-18483939 | It has been shown that serial passage using chicken embryos enforces the selection of adapted viruses and inevitably alters the genetic codes of the primary viral isolates, especially for genes involved in cell adsorption and viral replication [8, 9]. | [
"8",
"9",
"15",
"25",
"7",
"16",
"24",
"8",
"15"
] | 251 | 38,997 | 0 | false | It has been shown that serial passage using chicken embryos enforces the selection of adapted viruses and inevitably alters the genetic codes of the primary viral isolates, especially for genes involved in cell adsorption and viral replication. | [
"8, 9"
] | It has been shown that serial passage using chicken embryos enforces the selection of adapted viruses and inevitably alters the genetic codes of the primary viral isolates, especially for genes involved in cell adsorption and viral replication. | true | true | true | true | true | 6,714 |
2 | INTRODUCTION | 1 | 8 | [
"R8",
"R9",
"R15",
"R25",
"R7",
"R16",
"R24",
"R8",
"R15"
] | 19,793,537 | pmid-10366560|pmid-8116258|pmid-9060710|pmid-9101471|pmid-4565461|pmid-7609057|pmid-15332284|pmid-10366560|pmid-9060710|pmid-17296157|pmid-18483939|pmid-18645889|pmid-2545316|pmid-18483939 | The environment of the viral replication may also selectively modify the original cell tropism and pathogenesis of the isolated virus [15, 25]. | [
"8",
"9",
"15",
"25",
"7",
"16",
"24",
"8",
"15"
] | 143 | 38,998 | 0 | false | The environment of the viral replication may also selectively modify the original cell tropism and pathogenesis of the isolated virus. | [
"15, 25"
] | The environment of the viral replication may also selectively modify the original cell tropism and pathogenesis of the isolated virus. | true | true | true | true | true | 6,714 |
2 | INTRODUCTION | 1 | 7 | [
"R8",
"R9",
"R15",
"R25",
"R7",
"R16",
"R24",
"R8",
"R15"
] | 19,793,537 | pmid-10366560|pmid-8116258|pmid-9060710|pmid-9101471|pmid-4565461|pmid-7609057|pmid-15332284|pmid-10366560|pmid-9060710|pmid-17296157|pmid-18483939|pmid-18645889|pmid-2545316|pmid-18483939 | It has been shown that a serially embryo-passaged of infectious bronchitis viruses (IBV) M41 strain exhibited significantly attenuated pathogenesis within the oviduct compared to the parental strain [7]. | [
"8",
"9",
"15",
"25",
"7",
"16",
"24",
"8",
"15"
] | 203 | 38,999 | 1 | false | It has been shown that a serially embryo-passaged of infectious bronchitis viruses (IBV) M41 strain exhibited significantly attenuated pathogenesis within the oviduct compared to the parental strain. | [
"7"
] | It has been shown that a serially embryo-passaged of infectious bronchitis viruses (IBV) M41 strain exhibited significantly attenuated pathogenesis within the oviduct compared to the parental strain. | true | true | true | true | true | 6,714 |
2 | INTRODUCTION | 1 | 8 | [
"R8",
"R9",
"R15",
"R25",
"R7",
"R16",
"R24",
"R8",
"R15"
] | 19,793,537 | pmid-10366560|pmid-8116258|pmid-9060710|pmid-9101471|pmid-4565461|pmid-7609057|pmid-15332284|pmid-10366560|pmid-9060710|pmid-17296157|pmid-18483939|pmid-18645889|pmid-2545316|pmid-18483939 | In addition, egg-mediated epitope alterations in amplified isolates might attenuate the protective efficiency of these viruses when used to vaccinate against the challenge of a wild-type virulent strain [16, 24]. | [
"8",
"9",
"15",
"25",
"7",
"16",
"24",
"8",
"15"
] | 212 | 39,000 | 0 | false | In addition, egg-mediated epitope alterations in amplified isolates might attenuate the protective efficiency of these viruses when used to vaccinate against the challenge of a wild-type virulent strain. | [
"16, 24"
] | In addition, egg-mediated epitope alterations in amplified isolates might attenuate the protective efficiency of these viruses when used to vaccinate against the challenge of a wild-type virulent strain. | true | true | true | true | true | 6,714 |
2 | INTRODUCTION | 1 | 8 | [
"R8",
"R9",
"R15",
"R25",
"R7",
"R16",
"R24",
"R8",
"R15"
] | 19,793,537 | pmid-10366560|pmid-8116258|pmid-9060710|pmid-9101471|pmid-4565461|pmid-7609057|pmid-15332284|pmid-10366560|pmid-9060710|pmid-17296157|pmid-18483939|pmid-18645889|pmid-2545316|pmid-18483939 | For instance, after egg adaption, human influenza A virus, originally showing α2-6 sialic acid tropism only, exhibits increased hemagglutinin (HA) binding affinity to α2-3 sialic acid-containing gangliosides due to amino acid substitutions in the vicinity of the receptor binding site of the HA protein [8, 15]. | [
"8",
"9",
"15",
"25",
"7",
"16",
"24",
"8",
"15"
] | 311 | 39,001 | 0 | false | For instance, after egg adaption, human influenza A virus, originally showing α2-6 sialic acid tropism only, exhibits increased hemagglutinin (HA) binding affinity to α2-3 sialic acid-containing gangliosides due to amino acid substitutions in the vicinity of the receptor binding site of the HA protein. | [
"8, 15"
] | For instance, after egg adaption, human influenza A virus, originally showing α2-6 sialic acid tropism only, exhibits increased hemagglutinin (HA) binding affinity to α2-3 sialic acid-containing gangliosides due to amino acid substitutions in the vicinity of the receptor binding site of the HA protein. | true | true | true | true | true | 6,714 |
2 | INTRODUCTION | 1 | 8 | [
"R8",
"R9",
"R15",
"R25",
"R7",
"R16",
"R24",
"R8",
"R15"
] | 19,793,537 | pmid-10366560|pmid-8116258|pmid-9060710|pmid-9101471|pmid-4565461|pmid-7609057|pmid-15332284|pmid-10366560|pmid-9060710|pmid-17296157|pmid-18483939|pmid-18645889|pmid-2545316|pmid-18483939 | For primary viral isolates, providing natural host cells for replication might eliminate the selection pressure of an exotic growth environment and avert the alteration of cell tropism and consequent genomic mutations. | [
"8",
"9",
"15",
"25",
"7",
"16",
"24",
"8",
"15"
] | 218 | 39,002 | 0 | false | For primary viral isolates, providing natural host cells for replication might eliminate the selection pressure of an exotic growth environment and avert the alteration of cell tropism and consequent genomic mutations. | [] | For primary viral isolates, providing natural host cells for replication might eliminate the selection pressure of an exotic growth environment and avert the alteration of cell tropism and consequent genomic mutations. | true | true | true | true | true | 6,714 |
3 | INTRODUCTION | 1 | 33 | [
"R33"
] | 19,793,537 | pmid-18202946|pmid-17461266|pmid-16603523|pmid-16537586 | Recently, a study reported a primary culture system for tracheal epithelial cells from an embryonic day (E) 17 chick embryo, in which dissociated culture cells exhibited ciliary movement and were positive for the expression of pan-cytokeratin [33]. | [
"33"
] | 248 | 39,003 | 1 | false | Recently, a study reported a primary culture system for tracheal epithelial cells from an embryonic day (E) 17 chick embryo, in which dissociated culture cells exhibited ciliary movement and were positive for the expression of pan-cytokeratin. | [
"33"
] | Recently, a study reported a primary culture system for tracheal epithelial cells from an embryonic day (E) 17 chick embryo, in which dissociated culture cells exhibited ciliary movement and were positive for the expression of pan-cytokeratin. | true | true | true | true | true | 6,715 |
3 | INTRODUCTION | 1 | 33 | [
"R33"
] | 19,793,537 | pmid-18202946|pmid-17461266|pmid-16603523|pmid-16537586 | In addition, the global profile of mRNA expression in the cultured cells showed that cytokeratin 14 (K14), a basal cell marker, was highly expressed. | [
"33"
] | 149 | 39,004 | 0 | false | In addition, the global profile of mRNA expression in the cultured cells showed that cytokeratin 14 (K14), a basal cell marker, was highly expressed. | [] | In addition, the global profile of mRNA expression in the cultured cells showed that cytokeratin 14 (K14), a basal cell marker, was highly expressed. | true | true | true | true | true | 6,715 |
3 | INTRODUCTION | 1 | 33 | [
"R33"
] | 19,793,537 | pmid-18202946|pmid-17461266|pmid-16603523|pmid-16537586 | However, the protein expression of cell-type specific markers and the existence of mucin-secreting goblet cell are not well-characterized. | [
"33"
] | 138 | 39,005 | 0 | false | However, the protein expression of cell-type specific markers and the existence of mucin-secreting goblet cell are not well-characterized. | [] | However, the protein expression of cell-type specific markers and the existence of mucin-secreting goblet cell are not well-characterized. | true | true | true | true | true | 6,715 |
3 | INTRODUCTION | 1 | 33 | [
"R33"
] | 19,793,537 | pmid-18202946|pmid-17461266|pmid-16603523|pmid-16537586 | In this study, we developed a novel culture system to isolate, amplify and passage chicken tracheal epithelial cells in an efficient manner. | [
"33"
] | 140 | 39,006 | 0 | false | In this study, we developed a novel culture system to isolate, amplify and passage chicken tracheal epithelial cells in an efficient manner. | [] | In this study, we developed a novel culture system to isolate, amplify and passage chicken tracheal epithelial cells in an efficient manner. | true | true | true | true | true | 6,715 |
3 | INTRODUCTION | 1 | 33 | [
"R33"
] | 19,793,537 | pmid-18202946|pmid-17461266|pmid-16603523|pmid-16537586 | The avian tracheal epithelial (ATE) cell types were identified using immunocytostaining, and the ratio of cell types is statistically illustrated. | [
"33"
] | 146 | 39,007 | 0 | false | The avian tracheal epithelial (ATE) cell types were identified using immunocytostaining, and the ratio of cell types is statistically illustrated. | [] | The avian tracheal epithelial (ATE) cell types were identified using immunocytostaining, and the ratio of cell types is statistically illustrated. | true | true | true | true | true | 6,715 |
3 | INTRODUCTION | 1 | 33 | [
"R33"
] | 19,793,537 | pmid-18202946|pmid-17461266|pmid-16603523|pmid-16537586 | We further demonstrate that primary ATE cells support IBV replication. | [
"33"
] | 70 | 39,008 | 0 | false | We further demonstrate that primary ATE cells support IBV replication. | [] | We further demonstrate that primary ATE cells support IBV replication. | true | true | true | true | true | 6,715 |
3 | INTRODUCTION | 1 | 33 | [
"R33"
] | 19,793,537 | pmid-18202946|pmid-17461266|pmid-16603523|pmid-16537586 | The susceptible cell types and the effect of glycosaminoglycan (GAG) on IBV attachment to ATE cells was also investigated. | [
"33"
] | 122 | 39,009 | 0 | false | The susceptible cell types and the effect of glycosaminoglycan (GAG) on IBV attachment to ATE cells was also investigated. | [] | The susceptible cell types and the effect of glycosaminoglycan (GAG) on IBV attachment to ATE cells was also investigated. | true | true | true | true | true | 6,715 |
0 | DISCUSSION | 0 | null | null | 19,793,537 | null | In this study, we showed that primary ATE cells exhibit the same cell composition as tracheal epithelia and can be passaged and amplified in a convenient and efficient way. | null | 172 | 39,010 | 0 | false | null | null | In this study, we showed that primary ATE cells exhibit the same cell composition as tracheal epithelia and can be passaged and amplified in a convenient and efficient way. | true | true | true | true | true | 6,716 |
0 | DISCUSSION | 0 | null | null | 19,793,537 | null | These cells support IBV viral replication and viral release, providing an ideal system to amplify respiratory viruses and characterize their pathogenesis. | null | 154 | 39,011 | 0 | false | null | null | These cells support IBV viral replication and viral release, providing an ideal system to amplify respiratory viruses and characterize their pathogenesis. | true | true | true | true | true | 6,716 |
1 | DISCUSSION | 1 | 1 | [
"R1",
"R22",
"R3",
"R22",
"R3",
"R22",
"R12",
"R13",
"R22"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | In studies of tracheal infection, ciliated cells and goblet cells have been shown to be the major target cells of IBV [1, 22]. | [
"1",
"22",
"3",
"22",
"3",
"22",
"12",
"13",
"22"
] | 126 | 39,012 | 0 | false | In studies of tracheal infection, ciliated cells and goblet cells have been shown to be the major target cells of IBV. | [
"1, 22"
] | In studies of tracheal infection, ciliated cells and goblet cells have been shown to be the major target cells of IBV. | true | true | true | true | true | 6,717 |
1 | DISCUSSION | 1 | 1 | [
"R1",
"R22",
"R3",
"R22",
"R3",
"R22",
"R12",
"R13",
"R22"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | Our results with primary ATE cells also showed that IBV viral protein can be detected in both ciliated cells and goblet cells. | [
"1",
"22",
"3",
"22",
"3",
"22",
"12",
"13",
"22"
] | 126 | 39,013 | 0 | false | Our results with primary ATE cells also showed that IBV viral protein can be detected in both ciliated cells and goblet cells. | [] | Our results with primary ATE cells also showed that IBV viral protein can be detected in both ciliated cells and goblet cells. | true | true | true | true | true | 6,717 |
1 | DISCUSSION | 1 | 1 | [
"R1",
"R22",
"R3",
"R22",
"R3",
"R22",
"R12",
"R13",
"R22"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | This cell tropism may account for the pathogenesis of IBV, such as the ciliostasis in observed IBV-infected TOC and the reduction of sialic acid secretion [3, 22]. | [
"1",
"22",
"3",
"22",
"3",
"22",
"12",
"13",
"22"
] | 163 | 39,014 | 0 | false | This cell tropism may account for the pathogenesis of IBV, such as the ciliostasis in observed IBV-infected TOC and the reduction of sialic acid secretion. | [
"3, 22"
] | This cell tropism may account for the pathogenesis of IBV, such as the ciliostasis in observed IBV-infected TOC and the reduction of sialic acid secretion. | true | true | true | true | true | 6,717 |
1 | DISCUSSION | 1 | 1 | [
"R1",
"R22",
"R3",
"R22",
"R3",
"R22",
"R12",
"R13",
"R22"
] | 19,793,537 | pmid-10985803|pmid-12396356|pmid-17997603|pmid-15280485|pmid-3232319|pmid-1827578|pmid-3015104|pmid-3685630|pmid-19156578|pmid-18483939|pmid-17296157|pmid-18483939|pmid-17296157|pmid-18483939|pmid-14742263|NA|pmid-18483939 | In addition, we are the first to demonstrate that IBV does not appear to infect K14-positive basal cells. | [
"1",
"22",
"3",
"22",
"3",
"22",
"12",
"13",
"22"
] | 105 | 39,015 | 0 | false | In addition, we are the first to demonstrate that IBV does not appear to infect K14-positive basal cells. | [] | In addition, we are the first to demonstrate that IBV does not appear to infect K14-positive basal cells. | true | true | true | true | true | 6,717 |
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