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Volumn 32, Issue 1, 2002, Pages 116-127
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Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice
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Author keywords
[No Author keywords available]
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Indexed keywords
BINDING PROTEIN;
DYNACTIN;
PROTEIN;
PROTEIN CLIP 115;
PROTEIN CLIP 170;
PROTEIN CYLN2;
UNCLASSIFIED DRUG;
ALLELE;
ANIMAL BEHAVIOR;
ANIMAL CELL;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANIMAL TISSUE;
ARTICLE;
BRAIN DEVELOPMENT;
CHROMOSOME 7Q;
CONTROLLED STUDY;
DELETION MUTANT;
ELECTROPHYSIOLOGY;
GENE ACTIVITY;
GENE MUTATION;
GENE TARGETING;
GROWTH RETARDATION;
HEMIZYGOSITY;
HIPPOCAMPUS;
MICROTUBULE;
MOTOR COORDINATION;
MOUSE;
NERVE CELL DIFFERENTIATION;
NONHUMAN;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PRIORITY JOURNAL;
PROTEIN ANALYSIS;
RNA ANALYSIS;
WILLIAMS BEUREN SYNDROME;
ANIMALS;
BRAIN;
DYNEIN ATPASE;
GENE TARGETING;
HETEROZYGOTE;
MICE;
MICE, KNOCKOUT;
MICROTUBULE-ASSOCIATED PROTEINS;
MOTOR ACTIVITY;
MUTAGENESIS, SITE-DIRECTED;
NEOPLASM PROTEINS;
NERVE TISSUE PROTEINS;
PHENOTYPE;
WILLIAMS SYNDROME;
ANIMALIA;
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EID: 0036724985
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/ng954 Document Type: Article |
Times cited : (140)
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References (49)
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