The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans

Development

Volumn 130, Issue 20, 2003, Pages 5043-5052

  Piotrowski, Tatjana ^a,b   Ahn, Dae Gwon ^c   Schilling, Thomas F ^d   Nair, Sreelaja ^d   Ruvinsky, Ilya ^e   Geisler, Robert ^f   Rauch, Gerd Jörg ^f   Haffter, Pascal ^f   Zon, Leonard I ^g   Zhou, Yi ^g   Foott, Helen ^g   Dawid, Igor B ^a   Ho, Robert K ^c  

^a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e PRINCETON UNIVERSITY   (United States)

^f MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

^g BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

Aortic arches; DiGeorge syndrome; Endodermal pouches; Endothelin1; Pharyngeal arch development; tbx1; van gogh (vgo); Zebrafish

Indexed keywords

T BOX TRANSCRIPTION FACTOR;

ANIMAL CELL; ARTICLE; CELL TRANSPLANTATION; CLINICAL FEATURE; CONTROLLED STUDY; DIGEORGE SYNDROME; DNA LIBRARY; EMBRYO; EMBRYO DEVELOPMENT; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; HUMAN; IN SITU HYBRIDIZATION; LINKAGE ANALYSIS; MICROANGIOGRAPHY; MOLECULAR CLONING; NEURAL CREST CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PHARYNX; PHENOTYPE; PRIORITY JOURNAL; REGULATORY MECHANISM; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; ZEBRA FISH;

ANIMALIA; DANIO RERIO; VERTEBRATA;

EID: 0142149329     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.00704     Document Type: Article

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