Molecular cause of the severe functional deficiency in osteoclasts by an arginine deletion in the basic domain of Mi transcription factor

Journal of Bone and Mineral Metabolism

Volumn 19, Issue 3, 2001, Pages 183-187

  Nomura, Shintaro ^a   Sakuma, Takahiko ^a   Higashibata, Yuji ^a   Oboki, Keisuke ^a   Sato, Motohiko ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

Mi; Osteoclast; Transcription factor

Indexed keywords

ARGININE; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR MI; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; BINDING AFFINITY; CELL DIFFERENTIATION; CELL PROLIFERATION; CONFERENCE PAPER; DNA BINDING; GENE MUTATION; MOUSE; NONHUMAN; OSTEOCLAST; OSTEOPOROSIS; PRIORITY JOURNAL;

ACTIVE TRANSPORT, CELL NUCLEUS; ALLELES; ANIMALS; ARGININE; CELL NUCLEUS; DNA-BINDING PROTEINS; GENE DELETION; HELIX-LOOP-HELIX MOTIFS; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MICE; MICE, MUTANT STRAINS; MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; OSTEOCLASTS; OSTEOPETROSIS; TRANSCRIPTION FACTORS;

EID: 0034987174     PISSN: 09148779     EISSN: None     Source Type: Journal    
DOI: 10.1007/s007740170040     Document Type: Article

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