| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-152 |
Sentence |
denotes |
Sequence-variant repeats of MUC1 show higher conformational flexibility, are less densely O-glycosylated and induce differential B lymphocyte responses. |
| T1 |
0-152 |
Sentence |
denotes |
Sequence-variant repeats of MUC1 show higher conformational flexibility, are less densely O-glycosylated and induce differential B lymphocyte responses. |
| T1 |
0-152 |
Sentence |
denotes |
Sequence-variant repeats of MUC1 show higher conformational flexibility, are less densely O-glycosylated and induce differential B lymphocyte responses. |
| TextSentencer_T2 |
153-301 |
Sentence |
denotes |
The human epithelial cancer mucin MUC1 is able to break tolerance and to induce humoral immune responses in healthy subjects and in cancer patients. |
| T2 |
153-301 |
Sentence |
denotes |
The human epithelial cancer mucin MUC1 is able to break tolerance and to induce humoral immune responses in healthy subjects and in cancer patients. |
| T2 |
153-301 |
Sentence |
denotes |
The human epithelial cancer mucin MUC1 is able to break tolerance and to induce humoral immune responses in healthy subjects and in cancer patients. |
| TextSentencer_T3 |
302-510 |
Sentence |
denotes |
We recently showed that clusters of sequence-variant repeats are interspersed in the repeat domain of MUC1 at high frequency, which should contribute to the structural and immunological features of the mucin. |
| T3 |
302-510 |
Sentence |
denotes |
We recently showed that clusters of sequence-variant repeats are interspersed in the repeat domain of MUC1 at high frequency, which should contribute to the structural and immunological features of the mucin. |
| T3 |
302-510 |
Sentence |
denotes |
We recently showed that clusters of sequence-variant repeats are interspersed in the repeat domain of MUC1 at high frequency, which should contribute to the structural and immunological features of the mucin. |
| TextSentencer_T4 |
511-613 |
Sentence |
denotes |
Here we elucidated the potential effects exerted by sequence-variant repeats on their O-glycosylation. |
| T4 |
511-613 |
Sentence |
denotes |
Here we elucidated the potential effects exerted by sequence-variant repeats on their O-glycosylation. |
| T4 |
511-613 |
Sentence |
denotes |
Here we elucidated the potential effects exerted by sequence-variant repeats on their O-glycosylation. |
| TextSentencer_T5 |
614-958 |
Sentence |
denotes |
Evidence from in vitro glycosylation with polypeptide N-acetylgalactosaminyltransferases GalNAc-T1 and GalNAc-T2 in concert with mass spectrometric analyses of in vivo glycosylated MUC1 probes from transiently transfected HEK293 cells indicated reduced glycosylation densities of repeats with three concerted replacements: AHGVTSAPESRPAPGSTAPA. |
| T5 |
614-958 |
Sentence |
denotes |
Evidence from in vitro glycosylation with polypeptide N-acetylgalactosaminyltransferases GalNAc-T1 and GalNAc-T2 in concert with mass spectrometric analyses of in vivo glycosylated MUC1 probes from transiently transfected HEK293 cells indicated reduced glycosylation densities of repeats with three concerted replacements: AHGVTSAPESRPAPGSTAPA. |
| T5 |
614-958 |
Sentence |
denotes |
Evidence from in vitro glycosylation with polypeptide N-acetylgalactosaminyltransferases GalNAc-T1 and GalNAc-T2 in concert with mass spectrometric analyses of in vivo glycosylated MUC1 probes from transiently transfected HEK293 cells indicated reduced glycosylation densities of repeats with three concerted replacements: AHGVTSAPESRPAPGSTAPA. |
| TextSentencer_T6 |
959-1166 |
Sentence |
denotes |
The Pro to Ala replacement in STAPA exerts not only proximal effects on the ppGalNAc-T2 preferred site at -3 and -4, but also more distant effects on the ppGalNAc-T1 preferred site at -15 (TSAPESRPAPGSTAPA). |
| T6 |
959-1166 |
Sentence |
denotes |
The Pro to Ala replacement in STAPA exerts not only proximal effects on the ppGalNAc-T2 preferred site at -3 and -4, but also more distant effects on the ppGalNAc-T1 preferred site at -15 (TSAPESRPAPGSTAPA). |
| T6 |
959-1166 |
Sentence |
denotes |
The Pro to Ala replacement in STAPA exerts not only proximal effects on the ppGalNAc-T2 preferred site at -3 and -4, but also more distant effects on the ppGalNAc-T1 preferred site at -15 (TSAPESRPAPGSTAPA). |
| TextSentencer_T7 |
1167-1372 |
Sentence |
denotes |
We also examined the conformational changes of MUC1 glycopeptides induced by the concerted DT to ES replacements and revealed a higher conformational flexibility of ES/P peptides compared to DT/P peptides. |
| T7 |
1167-1372 |
Sentence |
denotes |
We also examined the conformational changes of MUC1 glycopeptides induced by the concerted DT to ES replacements and revealed a higher conformational flexibility of ES/P peptides compared to DT/P peptides. |
| T7 |
1167-1372 |
Sentence |
denotes |
We also examined the conformational changes of MUC1 glycopeptides induced by the concerted DT to ES replacements and revealed a higher conformational flexibility of ES/P peptides compared to DT/P peptides. |
| TextSentencer_T8 |
1373-1519 |
Sentence |
denotes |
Differences in conformational flexibilities and in O-glycosylation densities could underlie the observed differential humoral responses in humans. |
| T8 |
1373-1519 |
Sentence |
denotes |
Differences in conformational flexibilities and in O-glycosylation densities could underlie the observed differential humoral responses in humans. |
| T8 |
1373-1519 |
Sentence |
denotes |
Differences in conformational flexibilities and in O-glycosylation densities could underlie the observed differential humoral responses in humans. |
| TextSentencer_T9 |
1520-1718 |
Sentence |
denotes |
We were able to show that the natural immunoglobulin G (IgG) responses to the repeat domain of MUC1 in sera from nonmalignant control subjects are preferentially directed to variant repeat clusters. |
| T9 |
1520-1718 |
Sentence |
denotes |
We were able to show that the natural immunoglobulin G (IgG) responses to the repeat domain of MUC1 in sera from nonmalignant control subjects are preferentially directed to variant repeat clusters. |
| T9 |
1520-1718 |
Sentence |
denotes |
We were able to show that the natural immunoglobulin G (IgG) responses to the repeat domain of MUC1 in sera from nonmalignant control subjects are preferentially directed to variant repeat clusters. |
| TextSentencer_T10 |
1719-1847 |
Sentence |
denotes |
In contrast, the IgG response in patients with adenocarcinoma shifted to higher frequencies of preferential DTR peptide binding. |
| T10 |
1719-1847 |
Sentence |
denotes |
In contrast, the IgG response in patients with adenocarcinoma shifted to higher frequencies of preferential DTR peptide binding. |
| T10 |
1719-1847 |
Sentence |
denotes |
In contrast, the IgG response in patients with adenocarcinoma shifted to higher frequencies of preferential DTR peptide binding. |