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CYSTIC-FIBROSIS HETEROZYGOTE RESISTANCE TO CHOLERA-TOXIN IN THE CYSTIC-FIBROSIS MOUSE MODEL
Author(s): GABRIEL SE, BRIGMAN KN, KOLLER BH, BOUCHER RC, STUTTS MJ
Source: SCIENCE    Volume: 266    Issue: 5182    Pages: 107-109    Published: OCT 7 1994  
Times Cited: 226     References: 36     
Abstract: The effect of the number of cystic fibrosis (CF) alleles on cholera toxin (CT)-induced intestinal secretion was examined in the CF mouse model. CF mice that expressed no CF transmembrane conductance regulator (CFTR) protein did not secrete fluid in response to CT. Heterozygotes expressed 50 percent of the normal amount of CFTR protein in the intestinal epithelium and secreted 50 percent of the normal fluid and chloride ion in response to CT. This correlation between CFTR protein and CT-induced chloride ion and fluid secretion suggests that CF heterozygotes might possess a selective advantage of resistance to cholera.
Document Type: Article
Language: English
Reprint Address: GABRIEL, SE (reprint author), UNIV N CAROLINA, DEPT MED, CHAPEL HILL, NC 27599 USA
Publisher: AMER ASSOC ADVANCEMENT SCIENCE, 1200 NEW YORK AVE, NW, WASHINGTON, DC 20005
Subject Category: Multidisciplinary Sciences
IDS Number: PK582
ISSN: 0036-8075
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