Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome

Developmental Biology

Volumn 382, Issue 1, 2013, Pages 57-69

  Balow, Stephanie A ^a   Pierce, Lain X ^a   Zentner, Gabriel E ^a,c   Conrad, Patricia A ^a   Davis, Stephani ^d   Sabaawy, Hatem E ^d   McDermott, Brian M ^a,b   Scacheri, Peter C ^a,b  

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

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

^c Fred Hutchinson Cancer Research Center   (United States)

^d ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

Author keywords

Cell proliferation; CHARGE syndrome; Chd7; Fbxl10; RRNA; Zebrafish

Indexed keywords

BINDING PROTEIN; CHD7 PROTEIN; INK4AB PROTEIN; PROTEIN P15; PROTEIN P16; PROTEIN P21; PROTEIN P27; RIBOSOME RNA; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CARTILAGE; CELL PROLIFERATION; CHD7 GENE; CONTROLLED STUDY; CRANIOFACIAL DEVELOPMENT; DOSE RESPONSE; EMBRYO; EMBRYO DEATH; EMBRYO DEVELOPMENT; FBXL10 GENE; GENE SILENCING; KDM2BB GENE; NEURAL CREST; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REPRESSOR GENE; SYNDROME CHARGE; ZEBRA FISH;

DANIO RERIO;

EID: 84884418645     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2013.07.026     Document Type: Article

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