| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-122 |
Sentence |
denotes |
Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts. |
| T1 |
0-122 |
Sentence |
denotes |
Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts. |
| T1 |
0-122 |
Sentence |
denotes |
Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts. |
| TextSentencer_T2 |
123-242 |
Sentence |
denotes |
Patients with Type I congenital disorders of glycosylation (CDG-I) make incomplete lipid-linked oligosaccharides (LLO). |
| T2 |
123-242 |
Sentence |
denotes |
Patients with Type I congenital disorders of glycosylation (CDG-I) make incomplete lipid-linked oligosaccharides (LLO). |
| T2 |
123-242 |
Sentence |
denotes |
Patients with Type I congenital disorders of glycosylation (CDG-I) make incomplete lipid-linked oligosaccharides (LLO). |
| TextSentencer_T3 |
243-338 |
Sentence |
denotes |
These glycans are poorly transferred to proteins resulting in unoccupied glycosylation sequons. |
| T3 |
243-338 |
Sentence |
denotes |
These glycans are poorly transferred to proteins resulting in unoccupied glycosylation sequons. |
| T3 |
243-338 |
Sentence |
denotes |
These glycans are poorly transferred to proteins resulting in unoccupied glycosylation sequons. |
| TextSentencer_T4 |
339-496 |
Sentence |
denotes |
Mutations in phosphomannomutase (PMM2) cause CDG-Ia by reducing the activity of PMM, which converts mannose (Man)-6-P to Man-1-P before formation of GDP-Man. |
| T4 |
339-496 |
Sentence |
denotes |
Mutations in phosphomannomutase (PMM2) cause CDG-Ia by reducing the activity of PMM, which converts mannose (Man)-6-P to Man-1-P before formation of GDP-Man. |
| T4 |
339-777 |
Sentence |
denotes |
Mutations in phosphomannomutase (PMM2) cause CDG-Ia by reducing the activity of PMM, which converts mannose (Man)-6-P to Man-1-P before formation of GDP-Man. These patients have reduced Man-1-P and GDP-Man. To replenish intracellular Man-1-P pools in CDG-Ia cells, we synthesized two hydrophobic, membrane permeable acylated versions of Man-1-P and determined their ability to normalize LLO size and N-glycosylation in CDG-Ia fibroblasts. |
| TextSentencer_T5 |
497-545 |
Sentence |
denotes |
These patients have reduced Man-1-P and GDP-Man. |
| T5 |
497-545 |
Sentence |
denotes |
These patients have reduced Man-1-P and GDP-Man. |
| TextSentencer_T6 |
546-777 |
Sentence |
denotes |
To replenish intracellular Man-1-P pools in CDG-Ia cells, we synthesized two hydrophobic, membrane permeable acylated versions of Man-1-P and determined their ability to normalize LLO size and N-glycosylation in CDG-Ia fibroblasts. |
| T6 |
546-777 |
Sentence |
denotes |
To replenish intracellular Man-1-P pools in CDG-Ia cells, we synthesized two hydrophobic, membrane permeable acylated versions of Man-1-P and determined their ability to normalize LLO size and N-glycosylation in CDG-Ia fibroblasts. |
| TextSentencer_T7 |
778-1059 |
Sentence |
denotes |
Both compounds, compound I (diacetoxymethyl 2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl phosphate) (C-I) and compound II (diacetoxymethyl 2,3,4,6-tetra-O-ethyloxycarbonyl-alpha-D-mannopyranosyl phosphate) (C-II), contain two acetoxymethyl (CH2OAc) groups O-linked to phosphorous. |
| T5 |
778-1059 |
Sentence |
denotes |
Both compounds, compound I (diacetoxymethyl 2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl phosphate) (C-I) and compound II (diacetoxymethyl 2,3,4,6-tetra-O-ethyloxycarbonyl-alpha-D-mannopyranosyl phosphate) (C-II), contain two acetoxymethyl (CH2OAc) groups O-linked to phosphorous. |
| T7 |
778-1059 |
Sentence |
denotes |
Both compounds, compound I (diacetoxymethyl 2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl phosphate) (C-I) and compound II (diacetoxymethyl 2,3,4,6-tetra-O-ethyloxycarbonyl-alpha-D-mannopyranosyl phosphate) (C-II), contain two acetoxymethyl (CH2OAc) groups O-linked to phosphorous. |
| TextSentencer_T8 |
1060-1154 |
Sentence |
denotes |
C-I contains acetyl esters and C-II contains ethylcarbonate (CO2Et) esters on the Man residue. |
| T6 |
1060-1154 |
Sentence |
denotes |
C-I contains acetyl esters and C-II contains ethylcarbonate (CO2Et) esters on the Man residue. |
| T8 |
1060-1154 |
Sentence |
denotes |
C-I contains acetyl esters and C-II contains ethylcarbonate (CO2Et) esters on the Man residue. |
| TextSentencer_T9 |
1155-1249 |
Sentence |
denotes |
Both C-I and C-II normalized truncated LLO, but C-II was about 2-fold more efficient than C-I. |
| T9 |
1155-1249 |
Sentence |
denotes |
Both C-I and C-II normalized truncated LLO, but C-II was about 2-fold more efficient than C-I. |
| T7 |
1155-1409 |
Sentence |
denotes |
Both C-I and C-II normalized truncated LLO, but C-II was about 2-fold more efficient than C-I. C-II replenished the GDP-Man pool in CDG-Ia cells and was more efficiently incorporated into glycoproteins than exogenous Man at low concentrations (25-75 mM). |
| TextSentencer_T10 |
1250-1409 |
Sentence |
denotes |
C-II replenished the GDP-Man pool in CDG-Ia cells and was more efficiently incorporated into glycoproteins than exogenous Man at low concentrations (25-75 mM). |
| T10 |
1250-1409 |
Sentence |
denotes |
C-II replenished the GDP-Man pool in CDG-Ia cells and was more efficiently incorporated into glycoproteins than exogenous Man at low concentrations (25-75 mM). |
| TextSentencer_T11 |
1410-1513 |
Sentence |
denotes |
In a glycosylation assay of DNaseI in CDG-Ia cells, C-II restored glycosylation to control cell levels. |
| T8 |
1410-1513 |
Sentence |
denotes |
In a glycosylation assay of DNaseI in CDG-Ia cells, C-II restored glycosylation to control cell levels. |
| T11 |
1410-1513 |
Sentence |
denotes |
In a glycosylation assay of DNaseI in CDG-Ia cells, C-II restored glycosylation to control cell levels. |
| TextSentencer_T12 |
1514-1841 |
Sentence |
denotes |
C-II also corrected impaired LLO biosynthesis in cells from a Dolichol (Dol)-P-Man deficient patient (CDG-Ie) and partially corrected LLO in cells from an ALG12 mannosyltransferase-deficient patient (CDG-Ig), whereas cells from an ALG3-deficient patient (CDG-Id) and from an MPDU1-deficient patient (CDG-If) were not corrected. |
| T9 |
1514-1841 |
Sentence |
denotes |
C-II also corrected impaired LLO biosynthesis in cells from a Dolichol (Dol)-P-Man deficient patient (CDG-Ie) and partially corrected LLO in cells from an ALG12 mannosyltransferase-deficient patient (CDG-Ig), whereas cells from an ALG3-deficient patient (CDG-Id) and from an MPDU1-deficient patient (CDG-If) were not corrected. |
| T12 |
1514-1841 |
Sentence |
denotes |
C-II also corrected impaired LLO biosynthesis in cells from a Dolichol (Dol)-P-Man deficient patient (CDG-Ie) and partially corrected LLO in cells from an ALG12 mannosyltransferase-deficient patient (CDG-Ig), whereas cells from an ALG3-deficient patient (CDG-Id) and from an MPDU1-deficient patient (CDG-If) were not corrected. |
| TextSentencer_T13 |
1842-1962 |
Sentence |
denotes |
These results validate the general concept of using pro-Man-1-P substrates as potential therapeutics for CDG-I patients. |
| T10 |
1842-1962 |
Sentence |
denotes |
These results validate the general concept of using pro-Man-1-P substrates as potential therapeutics for CDG-I patients. |
| T13 |
1842-1962 |
Sentence |
denotes |
These results validate the general concept of using pro-Man-1-P substrates as potential therapeutics for CDG-I patients. |