Suppressive interactions between mutations located in the two nucleotide binding domains of CFTR

FEBS Letters

Volumn 473, Issue 2, 2000, Pages 149-153

  Wei, Lin ^a   Vankeerberghen, Anne ^a   Jaspers, Martine ^a   Cassiman, Jean Jacques ^a   Nilius, Bernd ^a   Cuppens, Harry ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

CFTR; Cystic fibrosis; Mutation; Polymorphism; Suppressive

Indexed keywords

CHLORIDE CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ANIMAL CELL; ARTICLE; BINDING SITE; CHLORIDE CURRENT; CYSTIC FIBROSIS; DNA POLYMORPHISM; GENE LOCUS; GENE MUTATION; HAPLOTYPE; IMMUNOPRECIPITATION; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; XENOPUS LAEVIS;

ALLELES; ANIMALS; BINDING SITES; COS CELLS; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; ELECTROPHYSIOLOGY; FEMALE; GENE FREQUENCY; GREEN FLUORESCENT PROTEINS; HAPLOTYPES; HUMANS; LUMINESCENT PROTEINS; MALE; MUTAGENESIS, SITE-DIRECTED; MUTATION; OOCYTES; RECOMBINANT FUSION PROTEINS; RNA, COMPLEMENTARY; SUPPRESSION, GENETIC; XENOPUS LAEVIS;

AMPHIBIA; ANIMALIA; REPTILIA; XENOPUS LAEVIS;

EID: 0034640496     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(00)01519-2     Document Type: Article

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