Interaction of the Ras-related protein associated with diabetes Rad and the putative tumor metastasis suppressor NM23 provides a novel mechanism of GTPase regulation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 26, 1999, Pages 14911-14918

  Zhu, Jianhua ^a   Tseng, Yu Hua ^a   Kantor, Jason D ^b   Rhodes, Christopher J ^a,c   Zetter, Bruce R ^b   Moyers, Julie S ^a   Kann, C Ronald ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c PACIFIC NORTHWEST RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; GUANOSINE TRIPHOSPHATASE; RAS PROTEIN;

ARTICLE; AUTOPHOSPHORYLATION; DIABETES MELLITUS; DNA SYNTHESIS; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME MECHANISM; ENZYME REGULATION; GENE CONTROL; GENE MUTATION; GLUCOSE METABOLISM; METASTASIS; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; TUMOR SUPPRESSOR GENE;

ANIMALS; DIABETES MELLITUS; DNA; ENZYME ACTIVATION; GENES, TUMOR SUPPRESSOR; GLUCOSE; GTP PHOSPHOHYDROLASES; GUANOSINE TRIPHOSPHATE; HUMANS; IMMEDIATE-EARLY PROTEINS; MODELS, BIOLOGICAL; MONOMERIC GTP-BINDING PROTEINS; NEOPLASM METASTASIS; NUCLEOSIDE-DIPHOSPHATE KINASE; PROTEIN BINDING; RAS PROTEINS; RATS; RATS, SPRAGUE-DAWLEY; TRANSCRIPTION FACTORS;

HEXAPODA;

EID: 0033592951     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.26.14911     Document Type: Article

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