Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome

Human Molecular Genetics

Volumn 15, Issue 2, 2006, Pages 259-271

  Antonellis, Anthony ^a   Bennett, William R ^b   Menheniott, Trevelyan R ^b   Prasad, Arjun B ^a,c   Lee Lin, Shih Queen ^a   Green, Eric D ^a   Paisley, Derek ^b   Kelsh, Robert N ^b   Pavan, William J ^a   Ward, Andrew ^b  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b University of Bath   (United Kingdom)

^c GEORGE WASHINGTON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR SOX10;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; COMPUTER MODEL; COMPUTER PROGRAM; CONTROLLED STUDY; GENE DELETION; GENE MUTATION; GENE SEQUENCE; HIRSCHSPRUNG DISEASE; INTESTINE INNERVATION; MELANOCYTE; MOUSE; MOUSE STRAIN; NEURAL CREST; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEQUENCE ANALYSIS; SKIN PIGMENTATION; WAARDENBURG SHAH SYNDROME; WAARDENBURG SYNDROME;

ALGORITHMS; ANIMALS; BASE SEQUENCE; BLOTTING, SOUTHERN; CELLS, CULTURED; CONSERVED SEQUENCE; DNA MUTATIONAL ANALYSIS; EMBRYO; GENE COMPONENTS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HIGH MOBILITY GROUP PROTEINS; IN SITU HYBRIDIZATION; LUCIFERASES; MICE; MICE, TRANSGENIC; MOLECULAR SEQUENCE DATA; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; SPECIES SPECIFICITY; TRANSCRIPTION FACTORS; TRANSGENES; WAARDENBURG'S SYNDROME;

ANIMALIA;

EID: 31144459828     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddi442     Document Type: Article

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