Abnormal skeletal patterning in embryos lacking a single Cbp allele: A partial similarity with Rubinstein-Taybi syndrome

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

Volumn 94, Issue 19, 1997, Pages 10215-10220

  Tanaka, Yasunori ^a,d   Naruse, Ichiro ^b   Maekawa, Toshio ^a   Masuya, Hiroshi ^c   Shiroishi, Toshihiko ^c   Ishii, Shunsuke ^a  

^a RIKEN TSUKUBA INSTITUTE   (Japan)

^b KYOTO UNIVERSITY   (Japan)

^c NATIONAL INSTITUTE OF GENETICS   (Japan)

^d UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

Bone morphogenetic protein; Coactivator; Haploinsufficiency; Pattern formation

Indexed keywords

BONE MORPHOGENETIC PROTEIN; DNA; RNA; TRANSCRIPTION FACTOR;

ALLELE; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; EMBRYO; EMBRYO PATTERN FORMATION; FETUS; GENE; GENE MUTATION; GENOTYPE; IN SITU HYBRIDIZATION; MOUSE; NONHUMAN; NORTHERN BLOTTING; PHENOTYPE; PRIORITY JOURNAL; RUBINSTEIN SYNDROME; SKELETON;

ANIMALS; BODY PATTERNING; BONE AND BONES; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; CELLS, CULTURED; FEMALE; HETEROZYGOTE; MALE; MICE; MICE, MUTANT STRAINS; MUTATION; PHENOTYPE; SYNDROME; TRANSFORMING GROWTH FACTOR BETA;

ANIMALIA; ERINACEIDAE; HEXAPODA; MAMMALIA;

EID: 0030923585     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.19.10215     Document Type: Article

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