A RUNX2/PEBP2αA/CBFA1 mutation in cleidocranial dysplasia revealing the link between the gene and Smad

Journal of Bone and Mineral Metabolism

Volumn 19, Issue 3, 2001, Pages 188-194

  Ito, Yoshiaki ^a   Zhang, Yu Wen ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

C2C12; RUNX2; Smad1

Indexed keywords

BONE MORPHOGENETIC PROTEIN; SMAD PROTEIN; TRANSFORMING GROWTH FACTOR BETA; DNA BINDING PROTEIN; SMAD3 PROTEIN; SMAD3 PROTEIN, HUMAN; SMAD3 PROTEIN, MOUSE; TRANSACTIVATOR PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX2; TUMOR PROTEIN;

CLEIDOCRANIAL DYSPLASIA; CONFERENCE PAPER; GENE MUTATION; GENETIC LINKAGE; HUMAN; PATHOGENESIS; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; TRANSACTIVATION; AMINO ACID SEQUENCE; ANIMAL; ARTICLE; BONE DEVELOPMENT; CELL STRAIN 3T3; CELL STRAIN COS1; CERCOPITHECUS; GENETICS; METABOLISM; MOLECULAR GENETICS; MOUSE; MUTATION;

3T3 CELLS; AMINO ACID SEQUENCE; ANIMALS; BONE MORPHOGENETIC PROTEINS; CERCOPITHECUS AETHIOPS; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; COS CELLS; DNA-BINDING PROTEINS; HUMANS; LINKAGE (GENETICS); MICE; MOLECULAR SEQUENCE DATA; MUTATION; NEOPLASM PROTEINS; OSTEOGENESIS; SMAD3 PROTEIN; TRANS-ACTIVATION (GENETICS); TRANS-ACTIVATORS; TRANSCRIPTION FACTORS;

EID: 0034743732     PISSN: 09148779     EISSN: None     Source Type: Journal    
DOI: 10.1007/s007740170041     Document Type: Conference Paper

References (37)

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