A role for CFTR in human autosomal dominant polycystic kidney disease

American Journal of Physiology - Cell Physiology

Volumn 270, Issue 1 39-1, 1996, Pages

  Hanaoka, Kazushige ^a   Devuyst, Olivier ^a   Schwiebert, Erik M ^a   Wilson, Patricia D ^a   Guggino, William B ^a,b  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

autosomal dominant polycystic kidney disease; chloride channels; cystic fibrosis transmembrane conductance regulator

Indexed keywords

CHLORIDE CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR;

APICAL MEMBRANE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CONTROLLED STUDY; ELECTROPHYSIOLOGY; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; KIDNEY POLYCYSTIC DISEASE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS;

EID: 0030065759     PISSN: 03636143     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpcell.1996.270.1.c389     Document Type: Article

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