Abnormal X chromosome inactivation and sex-specific gene dysregulation after ablation of FBXL10

Epigenetics and Chromatin

Volumn 9, Issue 1, 2016, Pages

  Boulard, Mathieu ^a   Edwards, John R ^b   Bestor, Timothy H ^a  

^a Columbia University ^*  (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

CpG rich promoters; FBXL11; Histone demethylase; Sexual dimorphism; X inactivation; Xist

Indexed keywords

CHROMOSOME PROTEIN; FBXL10 PROTEIN; RNA; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BINDING AFFINITY; BINDING SITE; CHROMOSOME ABERRATION; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; DISEASE ACTIVITY; DOWN REGULATION; EMBRYO; EMBRYOTOXICITY; FBXL10 1 GENE; FBXL10 2 GENE; FBXL10 GENE; FEMALE; GENE; GENE FUNCTION; MALE; MOLECULAR DYNAMICS; MOLECULAR PATHOLOGY; MOUSE; NEURAL TUBE DEFECT; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN FUNCTION; RNA BINDING; SEX DIFFERENCE; X CHROMOSOME INACTIVATION;

EID: 85007518901     PISSN: None     EISSN: 17568935     Source Type: Journal    
DOI: 10.1186/s13072-016-0069-1     Document Type: Article

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