The Krüppel-like Factor 15 as a Molecular Link between Myogenic Factors and a Chromosome 4q Transcriptional Enhancer Implicated in Facioscapulohumeral Dystrophy-Reference-Cited by-同舟云学术

The Krüppel-like Factor 15 as a Molecular Link between Myogenic Factors and a Chromosome 4q Transcriptional Enhancer Implicated in Facioscapulohumeral Dystrophy

Published:2011-12 Issue:52 Volume:286 Page:44620-44631
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Dmitriev Petr,Petrov Andrei,Ansseau Eugenie,Stankevicins Luiza,Charron Sébastien,Kim Elena,Bos Tomas Jan,Robert Thomas,Turki Ahmed,Coppée Frédérique,Belayew Alexandra,Lazar Vladimir,Carnac Gilles,Laoudj Dalila,Lipinski Marc,Vassetzky Yegor S.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference57 articles.

1. Genetic counselling in facioscapulohumeral muscular dystrophy.

2. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

3. Specific Sequence Variations within the 4q35 Region Are Associated with Facioscapulohumeral Muscular Dystrophy

4. Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle

5. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy

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