Correction of Lethal Intestinal Defect in a Mouse Model of Cystic Fibrosis by Human CFTR
Author:
Affiliation:
1. Children's Hospital Medical Center, Division of Pulmonary Biology, Cincinnati, OH 45229-3039, USA.
2. Department of Physiology and Biophysics, University of Alabama at Birmingham, Birmingham, AL 35294-0005, USA.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference9 articles.
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3. COHN, S.M., USE OF TRANSGENIC MICE TO MAP CIS-ACTING ELEMENTS IN THE INTESTINAL FATTY-ACID BINDING-PROTEIN GENE (FABPI) THAT CONTROL ITS CELL LINEAGE-SPECIFIC AND REGIONAL PATTERNS OF EXPRESSION ALONG THE DUODENAL COLONIC AND CRYPT VILLUS AXES OF THE GUT EPITHELIUM, JOURNAL OF CELL BIOLOGY 119: 27 (1992).
4. SIEMER, C, PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY 424: 321 (1993).
5. An Animal Model for Cystic Fibrosis Made by Gene Targeting
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