Cargando…
A genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci
BACKGROUND: Chromatin structure at a given site can differ between chromosome copies in a cell, and such imbalances in chromatin structure have been shown to be important in understanding the molecular mechanisms controlling several disease loci. Human genetic variation, DNA methylation, and disease...
Autores principales: | Prendergast, James G D, Tong, Pin, Hay, David C, Farrington, Susan M, Semple, Colin A M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3438052/ https://www.ncbi.nlm.nih.gov/pubmed/22607690 http://dx.doi.org/10.1186/1756-8935-5-6 |
Ejemplares similares
-
Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci
por: DeVries, Amber A, et al.
Publicado: (2022) -
Histone modifications in neurodifferentiation of embryonic stem cells
por: Huang, Min, et al.
Publicado: (2021) -
Side Effects: Substantial Non-Neutral Evolution Flanking Regulatory Sites
por: Prendergast, James G. D., et al.
Publicado: (2013) -
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
por: Wood, Andrew R., et al.
Publicado: (2011) -
The known genetic loci for telomere length may be involved in the modification of telomeres length after birth
por: Weng, Qiao, et al.
Publicado: (2016)