Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski−/− mice

Nature Genetics

Volumn 30, Issue 1, 2002, Pages 106-109

  Colmenares, Clemencia ^a   Heilstedt, Heidi A ^b   Shaffer, Lisa G ^b   Schwartz, Stuart ^c   Berk, Michael ^a   Murray, Jeffrey C ^d   Stavnezer, Ed ^e  

^a LERNER RESEARCH INSTITUTE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c CASE WESTERN RESERVE UNIVERSITY   (United States)

^d UNIVERSITY OF IOWA   (United States)

^e CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 1P; EXENCEPHALY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOSS; GENE OVEREXPRESSION; INCIDENCE; MONOSOMY; MOUSE; MUTATION; NEURAL TUBE DEFECT; NONHUMAN; PENETRANCE; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; PROTO ONCOGENE; SKI GENE; SYNDROME;

ABNORMALITIES, MULTIPLE; ANIMALS; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CHROMOSOMES, HUMAN, PAIR 1; DNA-BINDING PROTEINS; EMBRYONIC AND FETAL DEVELOPMENT; FACE; FETAL PROTEINS; GENE DELETION; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MODELS, GENETIC; MONOSOMY; NEURAL TUBE DEFECTS; PHENOTYPE; PROTO-ONCOGENE PROTEINS; PROTO-ONCOGENES; SPECIES SPECIFICITY; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0036334452     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng770     Document Type: Article

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