| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-64 |
Sentence |
denotes |
Characterization of human vascular endothelial cadherin glycans. |
| T1 |
0-64 |
Sentence |
denotes |
Characterization of human vascular endothelial cadherin glycans. |
| T1 |
0-64 |
Sentence |
denotes |
Characterization of human vascular endothelial cadherin glycans. |
| TextSentencer_T2 |
65-226 |
Sentence |
denotes |
The glycosylation pattern of human vascular endothelial cadherin (VE-cadherin), purified from cultured human umbilical cord vein endothelial cells, was analyzed. |
| T2 |
65-226 |
Sentence |
denotes |
The glycosylation pattern of human vascular endothelial cadherin (VE-cadherin), purified from cultured human umbilical cord vein endothelial cells, was analyzed. |
| T2 |
65-226 |
Sentence |
denotes |
The glycosylation pattern of human vascular endothelial cadherin (VE-cadherin), purified from cultured human umbilical cord vein endothelial cells, was analyzed. |
| TextSentencer_T3 |
227-398 |
Sentence |
denotes |
VE-cadherin was metabolically radiolabeled with d-[6-(3)H]glucosamine, isolated by immunoprecipitation, purified by SDS-PAGE and in-gel digested with endoproteinase Asp N. |
| T3 |
227-398 |
Sentence |
denotes |
VE-cadherin was metabolically radiolabeled with d-[6-(3)H]glucosamine, isolated by immunoprecipitation, purified by SDS-PAGE and in-gel digested with endoproteinase Asp N. |
| T3 |
227-514 |
Sentence |
denotes |
VE-cadherin was metabolically radiolabeled with d-[6-(3)H]glucosamine, isolated by immunoprecipitation, purified by SDS-PAGE and in-gel digested with endoproteinase Asp N. Oligosaccharides were sequentially released from resulting glycopeptides and analyzed by chromatographic profiling. |
| TextSentencer_T4 |
399-514 |
Sentence |
denotes |
Oligosaccharides were sequentially released from resulting glycopeptides and analyzed by chromatographic profiling. |
| T4 |
399-514 |
Sentence |
denotes |
Oligosaccharides were sequentially released from resulting glycopeptides and analyzed by chromatographic profiling. |
| TextSentencer_T5 |
515-685 |
Sentence |
denotes |
The results revealed that VE-cadherin carries predominantly sialylated diantennary and hybrid-type glycans in addition to some triantennary and high mannose-type species. |
| T4 |
515-685 |
Sentence |
denotes |
The results revealed that VE-cadherin carries predominantly sialylated diantennary and hybrid-type glycans in addition to some triantennary and high mannose-type species. |
| T5 |
515-685 |
Sentence |
denotes |
The results revealed that VE-cadherin carries predominantly sialylated diantennary and hybrid-type glycans in addition to some triantennary and high mannose-type species. |
| TextSentencer_T6 |
686-768 |
Sentence |
denotes |
Highly branched, tetraantennary oligosaccharides were found in trace amounts only. |
| T5 |
686-768 |
Sentence |
denotes |
Highly branched, tetraantennary oligosaccharides were found in trace amounts only. |
| T6 |
686-768 |
Sentence |
denotes |
Highly branched, tetraantennary oligosaccharides were found in trace amounts only. |
| TextSentencer_T7 |
769-984 |
Sentence |
denotes |
Immunohistochemical labeling of VE-cadherin and sialic acids displayed a codistribution along the intercellular junctions in endothelial cells of human umbilical arteries, veins, and cultured endothelial monolayers. |
| T6 |
769-984 |
Sentence |
denotes |
Immunohistochemical labeling of VE-cadherin and sialic acids displayed a codistribution along the intercellular junctions in endothelial cells of human umbilical arteries, veins, and cultured endothelial monolayers. |
| T7 |
769-984 |
Sentence |
denotes |
Immunohistochemical labeling of VE-cadherin and sialic acids displayed a codistribution along the intercellular junctions in endothelial cells of human umbilical arteries, veins, and cultured endothelial monolayers. |
| TextSentencer_T8 |
985-1165 |
Sentence |
denotes |
Ca(2+)-depletion, performed on cultured endothelial cells, resulted in a reversible complete disappearance of VE-cadherin and of almost all sialic acid staining from the junctions. |
| T7 |
985-1165 |
Sentence |
denotes |
Ca(2+)-depletion, performed on cultured endothelial cells, resulted in a reversible complete disappearance of VE-cadherin and of almost all sialic acid staining from the junctions. |
| T8 |
985-1165 |
Sentence |
denotes |
Ca(2+)-depletion, performed on cultured endothelial cells, resulted in a reversible complete disappearance of VE-cadherin and of almost all sialic acid staining from the junctions. |
| TextSentencer_T9 |
1166-1342 |
Sentence |
denotes |
Sialidase treatment of whole cells caused a change of VE-cadherin immunofluorescence from a continuous and netlike superstructural organization to a scattered inconsistent one. |
| T8 |
1166-1342 |
Sentence |
denotes |
Sialidase treatment of whole cells caused a change of VE-cadherin immunofluorescence from a continuous and netlike superstructural organization to a scattered inconsistent one. |
| T9 |
1166-1342 |
Sentence |
denotes |
Sialidase treatment of whole cells caused a change of VE-cadherin immunofluorescence from a continuous and netlike superstructural organization to a scattered inconsistent one. |
| TextSentencer_T10 |
1343-1422 |
Sentence |
denotes |
Hence, cell surface sialic acids might play a role in VE-cadherin organization. |
| T9 |
1343-1422 |
Sentence |
denotes |
Hence, cell surface sialic acids might play a role in VE-cadherin organization. |
| T10 |
1343-1422 |
Sentence |
denotes |
Hence, cell surface sialic acids might play a role in VE-cadherin organization. |