Imprint switch mechanism indicated by mutations in prader-willi and angelman syndromes
Author:
Publisher
Wiley
Subject
General Biochemistry, Genetics and Molecular Biology
Reference29 articles.
1. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
2. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences
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1. Genes controlling the activation of natural killer lymphocytes are epigenetically remodeled in intestinal cells from germ‐free mice;The FASEB Journal;2018-10-10
2. Mapping of Imprinted Quantitative Trait Loci Using Immortalized F2 Populations;PLoS ONE;2014-03-27
3. Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells;Journal of Human Genetics;2005-03
4. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS;Human Molecular Genetics;2001-03-01
5. Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes;Human Molecular Genetics;2001-02-01
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