A genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci

Epigenetics and Chromatin

Volumn 5, Issue 1, 2012, Pages

  Prendergast, James G D ^a   Tong, Pin ^b   Hay, David C ^c   Farrington, Susan M ^a   Semple, Colin A M ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b UNIVERSITY COLLEGE DUBLIN   (Ireland)

^c UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HISTONE;

ALLELE; ALLELE SPECIFIC HISTONE MODIFICATION; ARTICLE; CELLULAR DISTRIBUTION; DEVELOPMENTAL DISORDER; DNA METHYLATION; EMBRYO; EMBRYONIC STEM CELL; GENE DELETION; GENE EXPRESSION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SCREENING; GENOME IMPRINTING; HETEROZYGOTE; HISTONE MODIFICATION; HUMAN; HUMAN CELL; MARKER GENE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84861117171     PISSN: None     EISSN: 17568935     Source Type: Journal    
DOI: 10.1186/1756-8935-5-6     Document Type: Article

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