Dysfunctions in mice by NMDA receptor point mutations NR1(N598Q) and NR1(N598R)

Journal of Neuroscience

Volumn 20, Issue 7, 2000, Pages 2558-2566

  Single, Frank N ^a   Rozov, Andrei ^a   Burnashev, Nail ^a   Zimmermann, Frank ^b   Hanley, Daniel F ^c   Forrest, Douglas ^d   Curran, Tom ^e   Jensen, Vidar ^f   Hvalby, Øivind ^f   Sprengel, Rolf ^a   Seeburg, Peter H ^a  

^a MAX PLANCK INSTITUTE FOR MEDICAL RESEARCH   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^e ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^f UNIVERSITY OF OSLO   (Norway)

Author keywords

Barrel cortex; Ca2+ influx; Coincidence detection; Cre loxP; Gene targeting; LTP; Mg2+ block; NMDA receptor; Nurturing; Respiration

Indexed keywords

CALCIUM ION; COMPLEMENTARY DNA; MAGNESIUM ION; MESSENGER RNA; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; RECEPTOR SUBUNIT;

ALLELE; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN FUNCTION; CALCIUM TRANSPORT; CONTROLLED STUDY; GENE MUTATION; GENE TARGETING; GROWTH RETARDATION; LONG TERM POTENTIATION; MOUSE; NERVE CELL DIFFERENTIATION; NONHUMAN; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL;

EID: 17744418961     PISSN: 02706474     EISSN: None     Source Type: Journal    
DOI: 10.1523/jneurosci.20-07-02558.2000     Document Type: Article

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