| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-65 |
Sentence |
denotes |
Genomic organization and promoter activity of glucosidase I gene. |
| T1 |
0-65 |
Sentence |
denotes |
Genomic organization and promoter activity of glucosidase I gene. |
| T1 |
0-65 |
Sentence |
denotes |
Genomic organization and promoter activity of glucosidase I gene. |
| TextSentencer_T2 |
66-250 |
Sentence |
denotes |
Glucosidase I initiates the processing of asparagine (N-) linked glycoproteins by removing the distal alpha1,2-linked glucosyl residue of the tetradecasaccharide Glc(3)Man(9)GlcNAc(2). |
| T2 |
66-250 |
Sentence |
denotes |
Glucosidase I initiates the processing of asparagine (N-) linked glycoproteins by removing the distal alpha1,2-linked glucosyl residue of the tetradecasaccharide Glc(3)Man(9)GlcNAc(2). |
| T2 |
66-250 |
Sentence |
denotes |
Glucosidase I initiates the processing of asparagine (N-) linked glycoproteins by removing the distal alpha1,2-linked glucosyl residue of the tetradecasaccharide Glc(3)Man(9)GlcNAc(2). |
| TextSentencer_T3 |
251-359 |
Sentence |
denotes |
The gene encoding this enzyme was isolated and its structural organization and promoter activity determined. |
| T3 |
251-359 |
Sentence |
denotes |
The gene encoding this enzyme was isolated and its structural organization and promoter activity determined. |
| T3 |
251-359 |
Sentence |
denotes |
The gene encoding this enzyme was isolated and its structural organization and promoter activity determined. |
| TextSentencer_T4 |
360-570 |
Sentence |
denotes |
The major transcript for glucosidase I on northern blot appeared to be 3.1 kb; Southern blotting and DNA sequencing indicated the size of the gene to be 6.8 kb, comprising four exons separated by three introns. |
| T4 |
360-570 |
Sentence |
denotes |
The major transcript for glucosidase I on northern blot appeared to be 3.1 kb; Southern blotting and DNA sequencing indicated the size of the gene to be 6.8 kb, comprising four exons separated by three introns. |
| T4 |
360-570 |
Sentence |
denotes |
The major transcript for glucosidase I on northern blot appeared to be 3.1 kb; Southern blotting and DNA sequencing indicated the size of the gene to be 6.8 kb, comprising four exons separated by three introns. |
| TextSentencer_T5 |
571-704 |
Sentence |
denotes |
The first exon encodes the cytoplasmic tail and transmembrane domain; the fourth encodes the putative catalytic domain of the enzyme. |
| T5 |
571-704 |
Sentence |
denotes |
The first exon encodes the cytoplasmic tail and transmembrane domain; the fourth encodes the putative catalytic domain of the enzyme. |
| T5 |
571-704 |
Sentence |
denotes |
The first exon encodes the cytoplasmic tail and transmembrane domain; the fourth encodes the putative catalytic domain of the enzyme. |
| TextSentencer_T6 |
705-788 |
Sentence |
denotes |
Exon-intron junctions are flanked by consensus splice donor and acceptor sequences. |
| T6 |
705-788 |
Sentence |
denotes |
Exon-intron junctions are flanked by consensus splice donor and acceptor sequences. |
| T6 |
705-788 |
Sentence |
denotes |
Exon-intron junctions are flanked by consensus splice donor and acceptor sequences. |
| TextSentencer_T7 |
789-903 |
Sentence |
denotes |
Transcription initiation sites were mapped by primer extension, ribonuclease protection assay and RT-PCR analysis. |
| T7 |
789-903 |
Sentence |
denotes |
Transcription initiation sites were mapped by primer extension, ribonuclease protection assay and RT-PCR analysis. |
| T7 |
789-903 |
Sentence |
denotes |
Transcription initiation sites were mapped by primer extension, ribonuclease protection assay and RT-PCR analysis. |
| TextSentencer_T8 |
904-1038 |
Sentence |
denotes |
Primer extension results showed multiple initiation sites at -150, -156, and -272 bp relative to the translation initiation codon ATG. |
| T8 |
904-1038 |
Sentence |
denotes |
Primer extension results showed multiple initiation sites at -150, -156, and -272 bp relative to the translation initiation codon ATG. |
| T8 |
904-1038 |
Sentence |
denotes |
Primer extension results showed multiple initiation sites at -150, -156, and -272 bp relative to the translation initiation codon ATG. |
| TextSentencer_T9 |
1039-1196 |
Sentence |
denotes |
Sequence analysis of 5' flanking region showed no canonical TATA box, a high GC content, Sp1 and ETF binding sites (typical of a housekeeping gene promoter). |
| T9 |
1039-1196 |
Sentence |
denotes |
Sequence analysis of 5' flanking region showed no canonical TATA box, a high GC content, Sp1 and ETF binding sites (typical of a housekeeping gene promoter). |
| T9 |
1039-1196 |
Sentence |
denotes |
Sequence analysis of 5' flanking region showed no canonical TATA box, a high GC content, Sp1 and ETF binding sites (typical of a housekeeping gene promoter). |
| TextSentencer_T10 |
1197-1339 |
Sentence |
denotes |
Also noteworthy, the promoter region contains several generic STAT factor binding sites, one nearly perfect, and two half GR binding elements. |
| T10 |
1197-1339 |
Sentence |
denotes |
Also noteworthy, the promoter region contains several generic STAT factor binding sites, one nearly perfect, and two half GR binding elements. |
| T10 |
1197-1339 |
Sentence |
denotes |
Also noteworthy, the promoter region contains several generic STAT factor binding sites, one nearly perfect, and two half GR binding elements. |
| TextSentencer_T11 |
1340-1528 |
Sentence |
denotes |
Other cis- acting elements recognized by transcription factors such as AP-2, NF-kappaB, estrogen receptor, and progesterone receptor (PR) were also present in the putative promoter region. |
| T11 |
1340-1528 |
Sentence |
denotes |
Other cis- acting elements recognized by transcription factors such as AP-2, NF-kappaB, estrogen receptor, and progesterone receptor (PR) were also present in the putative promoter region. |
| T11 |
1340-1528 |
Sentence |
denotes |
Other cis- acting elements recognized by transcription factors such as AP-2, NF-kappaB, estrogen receptor, and progesterone receptor (PR) were also present in the putative promoter region. |
| TextSentencer_T12 |
1529-1770 |
Sentence |
denotes |
To determine the promoter activity, a construct encompassing the region between -2114 to -5 bp of the putative promoter was ligated to the chloramphenicol acetyltransferase (CAT) reporter plasmid and transiently transfected into COS 7 cells. |
| T12 |
1529-1770 |
Sentence |
denotes |
To determine the promoter activity, a construct encompassing the region between -2114 to -5 bp of the putative promoter was ligated to the chloramphenicol acetyltransferase (CAT) reporter plasmid and transiently transfected into COS 7 cells. |
| T12 |
1529-1770 |
Sentence |
denotes |
To determine the promoter activity, a construct encompassing the region between -2114 to -5 bp of the putative promoter was ligated to the chloramphenicol acetyltransferase (CAT) reporter plasmid and transiently transfected into COS 7 cells. |
| TextSentencer_T13 |
1771-1843 |
Sentence |
denotes |
CAT assay results clearly show transcriptional activity of the promoter. |
| T13 |
1771-1843 |
Sentence |
denotes |
CAT assay results clearly show transcriptional activity of the promoter. |
| T13 |
1771-1843 |
Sentence |
denotes |
CAT assay results clearly show transcriptional activity of the promoter. |