Subunit composition and pharmacological characterization of γ-aminobutyric acid type A receptors in frog pituitary melanotrophs

Endocrinology

Volumn 141, Issue 3, 2000, Pages 1083-1092

  Louiset, Estelle ^a   Mckernan, Ruth ^b   Sieghart, Werner ^c   Vaudry, Hubert ^a  

^a UNIVERSITÉ DE ROUEN   (France)

^b Merck Sharp & Dohme Limited   (United Kingdom)

^c MEDICAL UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID A RECEPTOR; 4' CHLORODIAZEPAM; 8 AZIDO 5,6 DIHYDRO 5 METHYL 6 OXO 4H IMIDAZO[1,5 A][1,4]BENZODIAZEPINE 3 CARBOXYLIC ACID ETHYL ESTER; BENZODIAZEPINE; BETA CARBOLINE 3 CARBAMIC ACID METHYL ESTER; CLONAZEPAM; DIAZEPAM; ETOMIDATE; FUROSEMIDE; MONOCLONAL ANTIBODY; N SEC BUTYL 1 (2 CHLOROPHENYL) N METHYL 3 ISOQUINOLINECARBOXAMIDE; RECEPTOR SUBUNIT; RO 54864; ZINC CHLORIDE; ZOLPIDEM;

ALLOSTERISM; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CHLORIDE CURRENT; CONTROLLED STUDY; DOSE RESPONSE; DRUG BINDING SITE; DRUG POTENCY; DRUG RECEPTOR BINDING; ENDOCRINE CELL; FROG; GABAERGIC SYSTEM; HYPOPHYSIS INTERMEDIATE LOBE; IMMUNOHISTOCHEMISTRY; MALE; NONHUMAN; PRIORITY JOURNAL;

EID: 0034465007     PISSN: 00137227     EISSN: None     Source Type: Journal    
DOI: 10.1210/endo.141.3.7397     Document Type: Article

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