Multiple Protein Domains Contribute to Nuclear Import and Cell Toxicity of DUX4, a Candidate Pathogenic Protein for Facioscapulohumeral Muscular Dystrophy
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference44 articles.
1. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy;JE Hewitt;Hum Mol Genet,1994
2. Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element;J Gabriels;Gene,1999
3. The FSHD associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subset of which are clustered on the short arms of the acrocentric chromosomes;R Lyle;Genomics,1995
4. Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy;J Clapp;Am J Hum Genet,2007
5. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit;JC van Deutekom;Hum Mol Genet,1993
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1. MATR3 is an endogenous inhibitor of DUX4 in FSHD muscular dystrophy;Cell Reports;2023-09
2. Influence of DUX4 Expression in Facioscapulohumeral Muscular Dystrophy and Possible Treatments;International Journal of Molecular Sciences;2023-05-30
3. Post‐Translational Modifications of the DUX4 Protein Impact Toxic Function in FSHD Cell Models;Annals of Neurology;2023-05-19
4. WDR5 is required for DUX4 expression and its pathological effects in FSHD muscular dystrophy;Nucleic Acids Research;2023-04-06
5. Posttranslational modifications of the DUX4 protein impact toxic function;2022-07-22
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