A desensitization-inhibiting mutation in the glutamate binding site of rat α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor subunits is dominant in heteromultimeric complexes

Neuroscience Letters

Volumn 277, Issue 3, 1999, Pages 161-164

  Thalhammer, Agnes ^a   Morth, Tanja ^a   Strutz, Nathalie ^a   Hollmann, Michael ^a  

^a MAX PLANCK INSTITUTE OF EXPERIMENTAL MEDICINE   (Germany)

Author keywords

Amino 3 hydroxy 5 methyl 4 isoxazole propionic acid receptors; Cyclothiazide; Desensitization; RNA editing; Xenopus oocyte

Indexed keywords

AMPA RECEPTOR; CYCLOTHIAZIDE; GLUTAMATE RECEPTOR AGONIST; GLUTAMIC ACID; ION CHANNEL; KAINIC ACID; LEUCINE; RECEPTOR SUBUNIT; TYROSINE;

ANIMAL CELL; ARTICLE; BINDING SITE; CONTROLLED STUDY; DESENSITIZATION; GENE MUTATION; MEMBRANE CURRENT; NONHUMAN; OOCYTE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN DOMAIN; SITE DIRECTED MUTAGENESIS; XENOPUS;

AMINO ACID SEQUENCE; ANIMALS; BENZOTHIADIAZINES; BINDING SITES; FEMALE; GENES, DOMINANT; GLUTAMIC ACID; MUTATION; OOCYTES; PROTEIN ISOFORMS; RATS; RECEPTORS, AMPA; RNA EDITING; XENOPUS LAEVIS;

EID: 0032693071     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(99)00885-X     Document Type: Article

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