| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-91 |
Sentence |
denotes |
Functional insertion of the SV40 large T oncogene in cystic fibrosis intestinal epithelium. |
| T1 |
0-91 |
Sentence |
denotes |
Functional insertion of the SV40 large T oncogene in cystic fibrosis intestinal epithelium. |
| T2 |
92-124 |
Sentence |
denotes |
Characterization of CFI-3 cells. |
| T2 |
92-124 |
Sentence |
denotes |
Characterization of CFI-3 cells. |
| T3 |
125-284 |
Sentence |
denotes |
Intestinal epithelial cells were isolated from a fetus with cystic fibrosis (CF) and transfected with a plasmid vector recombined with the ori- mutant of SV40. |
| T3 |
125-284 |
Sentence |
denotes |
Intestinal epithelial cells were isolated from a fetus with cystic fibrosis (CF) and transfected with a plasmid vector recombined with the ori- mutant of SV40. |
| T4 |
285-364 |
Sentence |
denotes |
A population of proliferative cells was then subcloned and designated as CFI-3. |
| T4 |
285-364 |
Sentence |
denotes |
A population of proliferative cells was then subcloned and designated as CFI-3. |
| T5 |
365-458 |
Sentence |
denotes |
These cells had a doubling time of 24 h and were maintained in culture for up to 25 passages. |
| T5 |
365-458 |
Sentence |
denotes |
These cells had a doubling time of 24 h and were maintained in culture for up to 25 passages. |
| T6 |
459-525 |
Sentence |
denotes |
At passage 8, CFI-3 cells did not produce any tumors in nude mice. |
| T6 |
459-525 |
Sentence |
denotes |
At passage 8, CFI-3 cells did not produce any tumors in nude mice. |
| T7 |
526-663 |
Sentence |
denotes |
Northern blot and immunofluorescence studies indicated that the extended lifespan of CFI-3 cells results in genomic insertion of SV40 LT. |
| T7 |
526-663 |
Sentence |
denotes |
Northern blot and immunofluorescence studies indicated that the extended lifespan of CFI-3 cells results in genomic insertion of SV40 LT. |
| T8 |
664-832 |
Sentence |
denotes |
Intestinal CFI-3 cells are epithelial, according to the expression of the human cytokeratin 18 gene and poorly differentiated by phase-contrast and electron microscopy. |
| T8 |
664-832 |
Sentence |
denotes |
Intestinal CFI-3 cells are epithelial, according to the expression of the human cytokeratin 18 gene and poorly differentiated by phase-contrast and electron microscopy. |
| T9 |
833-1040 |
Sentence |
denotes |
Functional membrane receptors activated by vasoactive intestinal peptide (VIP), its natural analogue pituitary adenylate cyclase activating peptide (PACAP-38), and isoproterenol were observed in CFI-3 cells. |
| T9 |
833-1040 |
Sentence |
denotes |
Functional membrane receptors activated by vasoactive intestinal peptide (VIP), its natural analogue pituitary adenylate cyclase activating peptide (PACAP-38), and isoproterenol were observed in CFI-3 cells. |
| T10 |
1041-1198 |
Sentence |
denotes |
Restriction fragment length polymorphism analysis of the PstI KM19 site revealed that the cftr locus was identical in the chorionic villi and in CFI-3 cells. |
| T10 |
1041-1198 |
Sentence |
denotes |
Restriction fragment length polymorphism analysis of the PstI KM19 site revealed that the cftr locus was identical in the chorionic villi and in CFI-3 cells. |
| T11 |
1199-1362 |
Sentence |
denotes |
The manifestation of CF in this family was not related to the common mutation delta F508, since this fetus was heterozygous for the substitutions S549N and N1303K. |
| T11 |
1199-1362 |
Sentence |
denotes |
The manifestation of CF in this family was not related to the common mutation delta F508, since this fetus was heterozygous for the substitutions S549N and N1303K. |
| T12 |
1363-1622 |
Sentence |
denotes |
Chloride transport, assessed by the 125I efflux, was induced in CFI-3 cells by the calcium inophore ionomycin, but not by the adenylate cyclase activator forskolin, and was inhibited by the chloride channel blocker 5-nitro-2-(3-phenylpropylamino)benzoic acid. |
| T12 |
1363-1622 |
Sentence |
denotes |
Chloride transport, assessed by the 125I efflux, was induced in CFI-3 cells by the calcium inophore ionomycin, but not by the adenylate cyclase activator forskolin, and was inhibited by the chloride channel blocker 5-nitro-2-(3-phenylpropylamino)benzoic acid. |
| T13 |
1623-1810 |
Sentence |
denotes |
These results were confirmed in patch clamp studies in which the cpt cAMP analogue failed to stimulate membrane currents, while the calcium ionophore ionomycin stimulated inward currents. |
| T13 |
1623-1810 |
Sentence |
denotes |
These results were confirmed in patch clamp studies in which the cpt cAMP analogue failed to stimulate membrane currents, while the calcium ionophore ionomycin stimulated inward currents. |
| T14 |
1811-2124 |
Sentence |
denotes |
We conclude that intestinal CFI-3 cells retain the CF phenotype relating to defective regulation of Cl- channels, and therefore constitute a suitable model, 1) for elucidating the function of CFTR protein, 2) developing new therapeutic agents, and 3) correcting the CF defect by gene replacement therapy in vitro. |
| T14 |
1811-2124 |
Sentence |
denotes |
We conclude that intestinal CFI-3 cells retain the CF phenotype relating to defective regulation of Cl- channels, and therefore constitute a suitable model, 1) for elucidating the function of CFTR protein, 2) developing new therapeutic agents, and 3) correcting the CF defect by gene replacement therapy in vitro. |