A conserved region of the R domain of cystic fibrosis transmembrane conductance regulator is important in processing and function

Journal of Biological Chemistry

Volumn 273, Issue 48, 1999, Pages 31759-31764

  Pasyk, Eva A ^b   Morin, Xenia K ^a   Zeman, Peter ^a   Garami, Elizabeth ^a   Galley, Kevin ^a   Huan, Ling Jun ^a   Wang, Yanchun ^a   Bear, Christine E ^a,b  

^a HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL; GLYCOPROTEIN P; NUCLEOTIDE BINDING PROTEIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL SURFACE; GENE MUTATION; IMMUNOFLUORESCENCE; MAMMAL; MEMBRANE CONDUCTANCE; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; SITE DIRECTED MUTAGENESIS; WESTERN BLOTTING; XENOPUS;

AMINO ACID SEQUENCE; ANIMALS; CELL LINE; CELL MEMBRANE; CONSERVED SEQUENCE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; HUMANS; ION CHANNEL GATING; KIDNEY; MEMBRANE POTENTIALS; MICE; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; OOCYTES; P-GLYCOPROTEIN; PHOSPHORYLATION; POINT MUTATION; RECOMBINANT PROTEINS; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; SERINE; TRANSFECTION; XENOPUS LAEVIS;

MAMMALIA;

EID: 0033610809     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.48.31759     Document Type: Article

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