Distinct global shifts in genomic binding profiles of limb malformation-Associated HOXD13 mutations

Genome Research

Volumn 23, Issue 12, 2013, Pages 2091-2102

  Ibrahim, Daniel M ^a,b   Hansen, Peter ^a   Rödelsperger, Christian ^a,d   Stiege, Asita C ^b   Doelken, Sandra C ^a   Horn, Denise ^a   Jäger, Marten ^a   Janetzki, Catrin ^a   Krawitz, Peter ^a   Leschik, Gundula ^a   Wagner, Florian ^c   Scheuer, Till ^a,b   Kegler, Mareen Schmidt Von ^a   Seemann, Petra ^a   Timmermann, Bernd ^b   Robinson, Peter N ^a,b   Mundlos, Stefan ^a,b   Hecht, Jochenl ^a,b  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^c ATLAS BIOLABS GMBH   (Germany)

^d MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMINE; HOMEOBOX PROTEIN D13; HOMEODOMAIN PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING SITE; BRACHYDACTYLY; CHROMATIN IMMUNOPRECIPITATION; CONTROLLED STUDY; DNA BINDING; EMBRYO; GENE EXPRESSION SYSTEM; GENE OVEREXPRESSION; HUMAN; LIMB DISEASE; LIMB MALFORMATION; MESENCHYMAL STEM CELL; MISSENSE MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; OLIGODACTYLIA; PRIORITY JOURNAL; SYNDACTYLY;

ANIMALS; BINDING SITES; CHICK EMBRYO; CHROMATIN IMMUNOPRECIPITATION; FEMALE; GENE EXPRESSION PROFILING; GENOME, HUMAN; GLUTAMINE; HOMEODOMAIN PROTEINS; HUMANS; LIMB DEFORMITIES, CONGENITAL; MESENCHYMAL STROMAL CELLS; MUTATION, MISSENSE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PAIRED BOX TRANSCRIPTION FACTORS; PHENOTYPE; RECEPTOR TYROSINE KINASE-LIKE ORPHAN RECEPTORS; TRANSCRIPTION FACTORS;

EID: 84890486930     PISSN: 10889051     EISSN: 15495469     Source Type: Journal    
DOI: 10.1101/gr.157610.113     Document Type: Article

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