| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-196 |
Sentence |
denotes |
Differential sialylation of cell surface glycoconjugates in a human B lymphoma cell line regulates susceptibility for CD95 (APO-1/Fas)-mediated apoptosis and for infection by a lymphotropic virus. |
| T1 |
0-196 |
Sentence |
denotes |
Differential sialylation of cell surface glycoconjugates in a human B lymphoma cell line regulates susceptibility for CD95 (APO-1/Fas)-mediated apoptosis and for infection by a lymphotropic virus. |
| TextSentencer_T2 |
197-337 |
Sentence |
denotes |
Sialic acid, as a terminal saccharide residue on cell surface glycoconjugates, plays an important role in a variety of biological processes. |
| T2 |
197-337 |
Sentence |
denotes |
Sialic acid, as a terminal saccharide residue on cell surface glycoconjugates, plays an important role in a variety of biological processes. |
| TextSentencer_T3 |
338-549 |
Sentence |
denotes |
In this study, we investigated subclones of the human B lymphoma cell line BJA-B for differences in the glycosylation of cell surface glycoconjugates, and studied the functional implications of such differences. |
| T3 |
338-549 |
Sentence |
denotes |
In this study, we investigated subclones of the human B lymphoma cell line BJA-B for differences in the glycosylation of cell surface glycoconjugates, and studied the functional implications of such differences. |
| TextSentencer_T4 |
550-771 |
Sentence |
denotes |
With respect to the expression level of most of the tested B cell-associated antigens, as well as the presence of penultimate saccharide moieties on oligosaccharide chains, subclones were phenotypically indistinguishable. |
| T4 |
550-771 |
Sentence |
denotes |
With respect to the expression level of most of the tested B cell-associated antigens, as well as the presence of penultimate saccharide moieties on oligosaccharide chains, subclones were phenotypically indistinguishable. |
| TextSentencer_T5 |
772-947 |
Sentence |
denotes |
Marked differences among subclones, however, were found in the overall level of glycoconjugate sialylation, involving both alpha-2,6 and alpha-2,3-linked sialic acid residues. |
| T5 |
772-947 |
Sentence |
denotes |
Marked differences among subclones, however, were found in the overall level of glycoconjugate sialylation, involving both alpha-2,6 and alpha-2,3-linked sialic acid residues. |
| TextSentencer_T6 |
948-1037 |
Sentence |
denotes |
Accordingly, subclones were classified as highly- (group I) or hyposialylated (group II). |
| T6 |
948-1037 |
Sentence |
denotes |
Accordingly, subclones were classified as highly- (group I) or hyposialylated (group II). |
| TextSentencer_T7 |
1038-1169 |
Sentence |
denotes |
The function of two sialic acid-dependent receptor-mediated processes is correlated with the sialylation status of BJA-B subclones. |
| T7 |
1038-1169 |
Sentence |
denotes |
The function of two sialic acid-dependent receptor-mediated processes is correlated with the sialylation status of BJA-B subclones. |
| TextSentencer_T8 |
1170-1432 |
Sentence |
denotes |
Susceptibility to and binding of the B lymphotropic papovavirus (LPV) was dependent on a high sialylation status of host cells, suggesting that differential sialylation in BJA-B cells can modulate LPV infection via its alpha-2,6-sialylated glycoprotein receptor. |
| T8 |
1170-1432 |
Sentence |
denotes |
Susceptibility to and binding of the B lymphotropic papovavirus (LPV) was dependent on a high sialylation status of host cells, suggesting that differential sialylation in BJA-B cells can modulate LPV infection via its alpha-2,6-sialylated glycoprotein receptor. |
| TextSentencer_T9 |
1433-1602 |
Sentence |
denotes |
CD95-mediated apoptosis, induced by either the human CD95 ligand or a cytotoxic anti-CD95 monoclonal antibody, was drastically enhanced in hyposialylated group II cells. |
| T9 |
1433-1602 |
Sentence |
denotes |
CD95-mediated apoptosis, induced by either the human CD95 ligand or a cytotoxic anti-CD95 monoclonal antibody, was drastically enhanced in hyposialylated group II cells. |
| TextSentencer_T10 |
1603-1732 |
Sentence |
denotes |
An increase in endogenous sialylation may be one antiapoptotic mechanism that converts tumor cells to a more malignant phenotype. |
| T10 |
1603-1732 |
Sentence |
denotes |
An increase in endogenous sialylation may be one antiapoptotic mechanism that converts tumor cells to a more malignant phenotype. |
| TextSentencer_T11 |
1733-1910 |
Sentence |
denotes |
To our knowledge, this is the first report demonstrating that differential sialylation in a clonal cell line may regulate the function of virus and signal-transducing receptors. |
| T11 |
1733-1910 |
Sentence |
denotes |
To our knowledge, this is the first report demonstrating that differential sialylation in a clonal cell line may regulate the function of virus and signal-transducing receptors. |