Cloning and functional characterization of two murine uridine nucleotide receptors reveal a potential target for correcting ion transport deficiency in cystic fibrosis gallbladder

Journal of Pharmacology and Experimental Therapeutics

Volumn 297, Issue 1, 2001, Pages 43-49

  Lazarowski, E R ^a   Rochelle, L G ^a   O'Neal, W K ^a   Ribeiro, C M P ^a   Grubb, B R ^a   Zhang, V ^a   Harden, T K ^a   Boucher, R C ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; CHLORIDE ION; INOSITOL PHOSPHATE; PURINE P2 RECEPTOR; URIDINE DIPHOSPHATE; URIDINE TRIPHOSPHATE;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CALCIUM MOBILIZATION; CHLORIDE TRANSPORT; CONTROLLED STUDY; CYSTIC FIBROSIS; DRUG RECEPTOR BINDING; GALLBLADDER EPITHELIUM; GENE DISRUPTION; ION TRANSPORT; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; STOMACH EPITHELIUM;

ADENOSINE TRIPHOSPHATE; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHLORIDE CHANNELS; CHLORIDES; CLONING, MOLECULAR; CYSTIC FIBROSIS; FEMALE; GALLBLADDER; MALE; MICE; MICE, INBRED DBA; MOLECULAR SEQUENCE DATA; RECEPTORS, PURINERGIC P2; RNA, MESSENGER;

EID: 0035087488     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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