d4z4

نتایج جستجو برای: d4z4

تعداد نتایج: 154 فیلتر نتایج به سال:

Mechanism and Timing of Mitotic Rearrangements in the Subtelomeric D4Z4 Repeat Involved in Facioscapulohumeral Muscular Dystrophy

Journal: :The American Journal of Human Genetics 2004

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Evolutionary Conservation of a Coding Function for D4Z4, the Tandem DNA Repeat Mutated in Facioscapulohumeral Muscular Dystrophy

Journal: :The American Journal of Human Genetics 2007

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NuRD and CAF-1-mediated silencing of the D4Z4 array is modulated by DUX4-induced MBD3L proteins

Journal: :eLife 2018

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FRG1P is localised in the nucleolus, Cajal bodies, and speckles.

Journal: :Journal of medical genetics 2004

S van Koningsbruggen R W Dirks A M Mommaas J J Onderwater G Deidda G W Padberg R R Frants S M van der Maarel

T he highly conserved facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) was initially cloned as candidate gene of unknown function for FSHD. To explore the biological function of the FRG1 protein (FRG1P), we studied its cellular localisation in untransfected and FRG1 transfected cell lines. In interphase cells, FRG1P is localised in the dense structures of the nucleolus, in Caj...

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