Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex

Human Molecular Genetics

Volumn 17, Issue 8, 2008, Pages 1175-1183

  Verstappen, Griet ^a,b   Van Grunsven, Leo A ^a,b   Michiels, Christine ^a,b   Van de Putte, Tom ^a,b   Souopgui, Jacob ^c   Van Damme, Jozef ^d,e   Bellefroid, Eric ^c   Vandekerckhove, Joël ^d,e   Huylebroeck, Danny ^a,b  

^a Lab of Devt Physiol/Molec Biol   (Belgium)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

^d Department of Medical Protein Research ^*  (Belgium)

^e GHENT UNIVERSITY   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; NUCLEOSOME REMODELING AND HISTONE DEACETYLATION COMPLEX PROTEIN; PROTEIN SUBUNIT; REPRESSOR PROTEIN; SMAD INTERACTING PROTEIN 1; UNCLASSIFIED DRUG; UVOMORULIN; ZINC FINGER PROTEIN;

AMINO TERMINAL SEQUENCE; ARTICLE; CELL STRAIN HEK293; CONTROLLED STUDY; EMBRYO; GENE MUTATION; GENE SEQUENCE; GENE TARGETING; GENETIC ASSOCIATION; HUMAN; HUMAN CELL; MALFORMATION SYNDROME; MASS SPECTROMETRY; MOLECULAR MECHANICS; MOWAT WILSON SYNDROME; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN ANALYSIS; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN MOTIF; PROTEIN PROTEIN INTERACTION; TRANSCRIPTION TERMINATION; XENOPUS;

ABNORMALITIES, MULTIPLE; ADENOSINE TRIPHOSPHATASES; ANIMALS; AUTOANTIGENS; CADHERINS; CELL LINE; DNA HELICASES; EMBRYO, NONMAMMALIAN; HISTONE DEACETYLASES; HUMANS; MENTAL RETARDATION; NERVE TISSUE PROTEINS; PROTEIN STRUCTURE, TERTIARY; RNA-BINDING PROTEINS; SYNDROME; XENOPUS;

ANIMALIA;

EID: 41849121175     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddn007     Document Type: Article

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