Channel β2-4 subunits fail to substitute for β1 in sensitizing BK channels to lithocholate

Biochemical and Biophysical Research Communications

Volumn 390, Issue 3, 2009, Pages 995-1000

  Bukiya, Anna N ^a   Vaithianathan, Thirumalini ^a   Toro, Ligia ^b   Dopico, Alejandro M ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

BK channel; KCNMB1; Lithocholic acid; Smooth muscle; Steroids

Indexed keywords

GLUCOCORTICOID; LARGE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL BETA SUBUNIT; LARGE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL BETA1 SUBUNIT; LARGE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL BETA2 SUBUNIT; LARGE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL BETA3 SUBUNIT; LARGE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL BETA4 SUBUNIT; LITHOCHOLIC ACID; MINERALOCORTICOID; SEX HORMONE; STEROID; UNCLASSIFIED DRUG; KCNMB1 PROTEIN, RAT; RECOMBINANT PROTEIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BRAIN ARTERY; CONCENTRATION RESPONSE; CONTROLLED STUDY; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; RAT; SENSITIZATION; SKELETAL MUSCLE; SMOOTH MUSCLE FIBER; XENOPUS LAEVIS; ANIMAL; DRUG POTENTIATION; GENETICS; METABOLISM;

RATTUS; XENOPUS LAEVIS;

ANIMALS; LARGE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNEL BETA SUBUNITS; LITHOCHOLIC ACID; OOCYTES; RATS; RECOMBINANT PROTEINS; STEROIDS; XENOPUS LAEVIS;

EID: 70449716868     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.10.091     Document Type: Article

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