Is CFTR Dysfunction in Cystic Fibrosis Compensated by MRPs?

Pediatric Research

Volumn 54, Issue 5, 2003, Pages 625-626

  Ito, Shinya ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; MULTIDRUG RESISTANCE PROTEIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

CHROMOSOME 7; CLINICAL GENETICS; CYSTIC FIBROSIS; GENE EXPRESSION; GENE MUTATION; HUMAN; NOTE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN FUNCTION;

CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EPITHELIAL CELLS; HUMANS; MUTATION; P-GLYCOPROTEINS;

EID: 0142148082     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/01.PDR.0000090925.31015.44     Document Type: Note

References (19)

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