Pharmacology of recombinant γ-aminobutyric acida receptors rendered diazepam-insensitive by point-mutated α-subunits

FEBS Letters

Volumn 431, Issue 3, 1998, Pages 400-404

  Benson, Jack A ^a   Löw, Karin ^a   Keist, Ruth ^a   Mohler, Hanns ^a   Rudolph, Uwe ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

Aminobutyric acid; Benzodiazepine; Central nervous system; Neurotransmitter; Receptor; Recombinant

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; DIAZEPAM; HISTIDINE; RECOMBINANT PROTEIN;

ANIMAL TISSUE; ARTICLE; BINDING SITE; CELL LINE; CODON; CONTROLLED STUDY; DRUG RECEPTOR BINDING; DRUG SENSITIVITY; HUMAN; HUMAN CELL; IN VITRO STUDY; KIDNEY CELL; NEUROTRANSMISSION; NONHUMAN; POINT MUTATION; PRIORITY JOURNAL; RAT;

AMINO ACID SEQUENCE; ANIMALS; AZIDES; BASE SEQUENCE; BENZODIAZEPINES; BENZODIAZEPINONES; CELL LINE; DIAZEPAM; HUMANS; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; OLIGODEOXYRIBONUCLEOTIDES; PATCH-CLAMP TECHNIQUES; RATS; RECEPTORS, GABA-A; RECOMBINANT PROTEINS;

ANIMALIA;

EID: 0345215147     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(98)00803-5     Document Type: Article

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