Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes-Reference-Cited by-同舟云学术

Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes

Published:2006-10 Issue:19 Volume:6 Page:5303-5321
ISSN:1615-9853
Container-title:PROTEOMICS
language:en
Short-container-title:Proteomics

Author:

Celegato Barbara,Capitanio Daniele,Pescatori Mario,Romualdi Chiara,Pacchioni Beniamina,Cagnin Stefano,Viganò Agnese,Colantoni Luca,Begum Shajna,Ricci Enzo,Wait Robin,Lanfranchi Gerolamo,Gelfi Cecilia

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Reference89 articles.

1. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

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

3. Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

4. Evidence for anticipation and association of deletion size with severity in facioscapulohumerd muscular dystrophy

5. Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

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