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A Distinct DNA-Methylation Boundary in the 5′- Upstream Sequence of the FMR1 Promoter Binds Nuclear Proteins and Is Lost in Fragile X Syndrome

We have discovered a distinct DNA-methylation boundary at a site between 650 and 800 nucleotides upstream of the CGG repeat in the first exon of the human FMR1 gene. This boundary, identified by bisulfite sequencing, is present in all human cell lines and cell types, irrespective of age, gender, and...

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Bibliografski detalji
Glavni autori: Naumann, Anja, Hochstein, Norbert, Weber, Stefanie, Fanning, Ellen, Doerfler, Walter
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2775827/
https://ncbi.nlm.nih.gov/pubmed/19853235
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2009.09.018
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