Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-124 |
Sentence |
denotes |
Production in yeast of alpha-galactosidase A, a lysosomal enzyme applicable to enzyme replacement therapy for Fabry disease. |
T1 |
0-124 |
Sentence |
denotes |
Production in yeast of alpha-galactosidase A, a lysosomal enzyme applicable to enzyme replacement therapy for Fabry disease. |
T1 |
0-124 |
Sentence |
denotes |
Production in yeast of alpha-galactosidase A, a lysosomal enzyme applicable to enzyme replacement therapy for Fabry disease. |
TextSentencer_T2 |
125-345 |
Sentence |
denotes |
A mammalian-like sugar moiety was created in glycoprotein by Saccharomyces cerevisiae in combination with bacterial alpha-mannosidase to produce a more economic enzyme replacement therapy for patients with Fabry disease. |
T2 |
125-345 |
Sentence |
denotes |
A mammalian-like sugar moiety was created in glycoprotein by Saccharomyces cerevisiae in combination with bacterial alpha-mannosidase to produce a more economic enzyme replacement therapy for patients with Fabry disease. |
T2 |
125-345 |
Sentence |
denotes |
A mammalian-like sugar moiety was created in glycoprotein by Saccharomyces cerevisiae in combination with bacterial alpha-mannosidase to produce a more economic enzyme replacement therapy for patients with Fabry disease. |
TextSentencer_T3 |
346-497 |
Sentence |
denotes |
We introduced the human alpha-galactosidase A (alpha-GalA) gene into an S. cerevisiae mutant that was deficient in the outer chains of N-linked mannan. |
T3 |
346-497 |
Sentence |
denotes |
We introduced the human alpha-galactosidase A (alpha-GalA) gene into an S. cerevisiae mutant that was deficient in the outer chains of N-linked mannan. |
T3 |
346-497 |
Sentence |
denotes |
We introduced the human alpha-galactosidase A (alpha-GalA) gene into an S. cerevisiae mutant that was deficient in the outer chains of N-linked mannan. |
TextSentencer_T4 |
498-620 |
Sentence |
denotes |
The recombinant alpha-GalA contained both neutral (Man(8)GlcNAc(2)) and acidic ([Man-P](1-2)Man(8)GlcNAc(2)) sugar chains. |
T4 |
498-620 |
Sentence |
denotes |
The recombinant alpha-GalA contained both neutral (Man(8)GlcNAc(2)) and acidic ([Man-P](1-2)Man(8)GlcNAc(2)) sugar chains. |
T4 |
498-620 |
Sentence |
denotes |
The recombinant alpha-GalA contained both neutral (Man(8)GlcNAc(2)) and acidic ([Man-P](1-2)Man(8)GlcNAc(2)) sugar chains. |
TextSentencer_T5 |
621-899 |
Sentence |
denotes |
Because an efficient incorporation of alpha-GalA into lysosomes of human cells requires mannose-6-phosphate (Man-6-P) residues that should be recognized by the specific receptor, we trimmed down the sugar chains of the alpha-GalA by a newly isolated bacterial alpha-mannosidase. |
T5 |
621-899 |
Sentence |
denotes |
Because an efficient incorporation of alpha-GalA into lysosomes of human cells requires mannose-6-phosphate (Man-6-P) residues that should be recognized by the specific receptor, we trimmed down the sugar chains of the alpha-GalA by a newly isolated bacterial alpha-mannosidase. |
T5 |
621-899 |
Sentence |
denotes |
Because an efficient incorporation of alpha-GalA into lysosomes of human cells requires mannose-6-phosphate (Man-6-P) residues that should be recognized by the specific receptor, we trimmed down the sugar chains of the alpha-GalA by a newly isolated bacterial alpha-mannosidase. |
TextSentencer_T6 |
900-1113 |
Sentence |
denotes |
Treatment of the alpha-GalA with the alpha-mannosidase resulted in the exposure of a Man-6-P residue on a nonreduced end of oligosaccharide chains after the removal of phosphodiester-linked nonreduced-end mannose. |
T6 |
900-1113 |
Sentence |
denotes |
Treatment of the alpha-GalA with the alpha-mannosidase resulted in the exposure of a Man-6-P residue on a nonreduced end of oligosaccharide chains after the removal of phosphodiester-linked nonreduced-end mannose. |
T6 |
900-1113 |
Sentence |
denotes |
Treatment of the alpha-GalA with the alpha-mannosidase resulted in the exposure of a Man-6-P residue on a nonreduced end of oligosaccharide chains after the removal of phosphodiester-linked nonreduced-end mannose. |
TextSentencer_T7 |
1114-1224 |
Sentence |
denotes |
The treated alpha-GalA was efficiently incorporated into fibroblasts derived from patients with Fabry disease. |
T7 |
1114-1224 |
Sentence |
denotes |
The treated alpha-GalA was efficiently incorporated into fibroblasts derived from patients with Fabry disease. |
T7 |
1114-1224 |
Sentence |
denotes |
The treated alpha-GalA was efficiently incorporated into fibroblasts derived from patients with Fabry disease. |
TextSentencer_T8 |
1225-1356 |
Sentence |
denotes |
The uptake was three to four times higher than that of the nontreated alpha-GalA and was inhibited by the addition of 5 mM Man-6-P. |
T8 |
1225-1356 |
Sentence |
denotes |
The uptake was three to four times higher than that of the nontreated alpha-GalA and was inhibited by the addition of 5 mM Man-6-P. |
T8 |
1225-1497 |
Sentence |
denotes |
The uptake was three to four times higher than that of the nontreated alpha-GalA and was inhibited by the addition of 5 mM Man-6-P. Incorporated alpha-GalA was targeted to the lysosome, and hydrolyzed ceramide trihexoside accumulated in the Fabry fibroblasts after 5 days. |
TextSentencer_T9 |
1357-1497 |
Sentence |
denotes |
Incorporated alpha-GalA was targeted to the lysosome, and hydrolyzed ceramide trihexoside accumulated in the Fabry fibroblasts after 5 days. |
T9 |
1357-1497 |
Sentence |
denotes |
Incorporated alpha-GalA was targeted to the lysosome, and hydrolyzed ceramide trihexoside accumulated in the Fabry fibroblasts after 5 days. |
TextSentencer_T10 |
1498-1607 |
Sentence |
denotes |
This method provides an effective and economic therapy for many lysosomal disorders, including Fabry disease. |
T9 |
1498-1607 |
Sentence |
denotes |
This method provides an effective and economic therapy for many lysosomal disorders, including Fabry disease. |
T10 |
1498-1607 |
Sentence |
denotes |
This method provides an effective and economic therapy for many lysosomal disorders, including Fabry disease. |