Additional disruption of the ClC-2 Cl- channel does not exacerbate the cystic fibrosis phenotype of cystic fibrosis transmembrane conductance regulator mouse models

Journal of Biological Chemistry

Volumn 279, Issue 21, 2004, Pages 22276-22283

  Zdebik, Anselm A ^a   Cuffe, John E ^b   Bertog, Marko ^b,c   Korbmacher, Christoph ^b,c   Jentsch, Thomas J ^a  

^a Zentrum Molec Neurobiologie Hamburg   (Germany)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c Inst Zellulare und Molec Physiol   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GASTROENTEROLOGY; GENES; MUTAGENESIS; RESPIRATORY SYSTEM; TISSUE;

CYSTIC FIBROSIS; PHENOTYES;

BIOLOGICAL MEMBRANES;

CHLORIDE CHANNEL; CYCLIC AMP; PHENYLALANINE; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ANIMAL TISSUE; ARTICLE; BASOLATERAL MEMBRANE; CHLORIDE CHANNEL CLC 2; CHLORIDE TRANSPORT; COLON MUCOSA; CONTROLLED STUDY; CYSTIC FIBROSIS; EPITHELIUM CELL; GENE DELETION; GENE DISRUPTION; INTESTINE; LUNG; MOUSE; MUTATION; NONHUMAN; PANCREAS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SURVIVAL;

ANIMALIA;

EID: 2542466643     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M309899200     Document Type: Article

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