| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-84 |
Sentence |
denotes |
Metabolic glycoengineering of mesenchymal stromal cells with N-propanoylmannosamine. |
| T1 |
0-84 |
Sentence |
denotes |
Metabolic glycoengineering of mesenchymal stromal cells with N-propanoylmannosamine. |
| T1 |
0-84 |
Sentence |
denotes |
Metabolic glycoengineering of mesenchymal stromal cells with N-propanoylmannosamine. |
| TextSentencer_T2 |
85-214 |
Sentence |
denotes |
There is an increasing interest in the modification of cell surface glycosylation to improve the properties of therapeutic cells. |
| T2 |
85-214 |
Sentence |
denotes |
There is an increasing interest in the modification of cell surface glycosylation to improve the properties of therapeutic cells. |
| T2 |
85-214 |
Sentence |
denotes |
There is an increasing interest in the modification of cell surface glycosylation to improve the properties of therapeutic cells. |
| TextSentencer_T3 |
215-306 |
Sentence |
denotes |
For example, glycosylation affects the biodistribution of mesenchymal stromal cells (MSCs). |
| T3 |
215-306 |
Sentence |
denotes |
For example, glycosylation affects the biodistribution of mesenchymal stromal cells (MSCs). |
| T3 |
215-306 |
Sentence |
denotes |
For example, glycosylation affects the biodistribution of mesenchymal stromal cells (MSCs). |
| TextSentencer_T4 |
307-381 |
Sentence |
denotes |
Metabolic glycoengineering is an efficient way to modify the cell surface. |
| T4 |
307-381 |
Sentence |
denotes |
Metabolic glycoengineering is an efficient way to modify the cell surface. |
| T4 |
307-381 |
Sentence |
denotes |
Metabolic glycoengineering is an efficient way to modify the cell surface. |
| TextSentencer_T5 |
382-555 |
Sentence |
denotes |
The mammalian biosynthetic machinery tolerates the unnatural sialic acid precursor, N-propanoylmannosamine (ManNProp), and incorporates it into cell surface glycoconjugates. |
| T5 |
382-555 |
Sentence |
denotes |
The mammalian biosynthetic machinery tolerates the unnatural sialic acid precursor, N-propanoylmannosamine (ManNProp), and incorporates it into cell surface glycoconjugates. |
| T5 |
382-555 |
Sentence |
denotes |
The mammalian biosynthetic machinery tolerates the unnatural sialic acid precursor, N-propanoylmannosamine (ManNProp), and incorporates it into cell surface glycoconjugates. |
| TextSentencer_T6 |
556-799 |
Sentence |
denotes |
We show here by mass spectrometric analysis of cell surface N-glycans that about half of N-acetylneuraminic acid was replaced by N-propanoylneuraminic acid in the N-glycans of human umbilical cord blood-derived MSCs supplemented with ManNProp. |
| T6 |
556-799 |
Sentence |
denotes |
We show here by mass spectrometric analysis of cell surface N-glycans that about half of N-acetylneuraminic acid was replaced by N-propanoylneuraminic acid in the N-glycans of human umbilical cord blood-derived MSCs supplemented with ManNProp. |
| T6 |
556-799 |
Sentence |
denotes |
We show here by mass spectrometric analysis of cell surface N-glycans that about half of N-acetylneuraminic acid was replaced by N-propanoylneuraminic acid in the N-glycans of human umbilical cord blood-derived MSCs supplemented with ManNProp. |
| TextSentencer_T7 |
800-846 |
Sentence |
denotes |
In addition, the N-glycan profile was altered. |
| T7 |
800-846 |
Sentence |
denotes |
In addition, the N-glycan profile was altered. |
| T7 |
800-846 |
Sentence |
denotes |
In addition, the N-glycan profile was altered. |
| TextSentencer_T8 |
847-941 |
Sentence |
denotes |
ManNProp-supplemented cells had more multiply fucosylated N-glycan species than control cells. |
| T8 |
847-941 |
Sentence |
denotes |
ManNProp-supplemented cells had more multiply fucosylated N-glycan species than control cells. |
| T8 |
847-941 |
Sentence |
denotes |
ManNProp-supplemented cells had more multiply fucosylated N-glycan species than control cells. |
| TextSentencer_T9 |
942-1087 |
Sentence |
denotes |
The fucosylated epitopes were shown in tandem mass spectrometric analysis to be Lewis x or blood group H epitopes, but not sialyl Lewis x (sLex). |
| T9 |
942-1087 |
Sentence |
denotes |
The fucosylated epitopes were shown in tandem mass spectrometric analysis to be Lewis x or blood group H epitopes, but not sialyl Lewis x (sLex). |
| T9 |
942-1087 |
Sentence |
denotes |
The fucosylated epitopes were shown in tandem mass spectrometric analysis to be Lewis x or blood group H epitopes, but not sialyl Lewis x (sLex). |
| TextSentencer_T10 |
1088-1212 |
Sentence |
denotes |
The amounts of tri- and tetra-antennary and polylactosamine-containing N-glycans also increased in ManNProp supplementation. |
| T10 |
1088-1212 |
Sentence |
denotes |
The amounts of tri- and tetra-antennary and polylactosamine-containing N-glycans also increased in ManNProp supplementation. |
| T10 |
1088-1212 |
Sentence |
denotes |
The amounts of tri- and tetra-antennary and polylactosamine-containing N-glycans also increased in ManNProp supplementation. |
| TextSentencer_T11 |
1213-1376 |
Sentence |
denotes |
In accordance with previous studies of other cell types, increased expression of the sLex epitope in ManNProp-supplemented MSCs was demonstrated by flow cytometry. |
| T11 |
1213-1376 |
Sentence |
denotes |
In accordance with previous studies of other cell types, increased expression of the sLex epitope in ManNProp-supplemented MSCs was demonstrated by flow cytometry. |
| T11 |
1213-1376 |
Sentence |
denotes |
In accordance with previous studies of other cell types, increased expression of the sLex epitope in ManNProp-supplemented MSCs was demonstrated by flow cytometry. |
| TextSentencer_T12 |
1377-1599 |
Sentence |
denotes |
In light of the N-glycan analysis, the sLex epitope in these cells is likely to be carried by O-glycans or glycolipids. sLex has been shown to target MSCs to bone marrow, which may be desirable in therapeutic applications. |
| T12 |
1377-1599 |
Sentence |
denotes |
In light of the N-glycan analysis, the sLex epitope in these cells is likely to be carried by O-glycans or glycolipids. sLex has been shown to target MSCs to bone marrow, which may be desirable in therapeutic applications. |
| T12 |
1377-1599 |
Sentence |
denotes |
In light of the N-glycan analysis, the sLex epitope in these cells is likely to be carried by O-glycans or glycolipids. sLex has been shown to target MSCs to bone marrow, which may be desirable in therapeutic applications. |
| TextSentencer_T13 |
1600-1843 |
Sentence |
denotes |
The present results represent the first structural analysis of an N-glycome of ManNProp-supplemented cells and demonstrate the feasibility of modifying cell surface glycosylation of therapeutic cells by this type of metabolic glycoengineering. |
| T13 |
1600-1843 |
Sentence |
denotes |
The present results represent the first structural analysis of an N-glycome of ManNProp-supplemented cells and demonstrate the feasibility of modifying cell surface glycosylation of therapeutic cells by this type of metabolic glycoengineering. |
| T13 |
1600-1843 |
Sentence |
denotes |
The present results represent the first structural analysis of an N-glycome of ManNProp-supplemented cells and demonstrate the feasibility of modifying cell surface glycosylation of therapeutic cells by this type of metabolic glycoengineering. |