Wordt geladen...

Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy

Repression of repetitive elements is crucial to preserve genome integrity and has been traditionally ascribed to constitutive heterochromatin pathways. FacioScapuloHumeral Muscular Dystrophy (FSHD), one of the most common myopathies, is characterized by a complex interplay of genetic and epigenetic...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Gepubliceerd in:Hum Mol Genet
Hoofdauteurs: Casa, Valentina, Runfola, Valeria, Micheloni, Stefano, Aziz, Arif, Dilworth, F. Jeffrey, Gabellini, Davide
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2017
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5409123/
https://ncbi.nlm.nih.gov/pubmed/28040729
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw426
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!