Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers-Reference-Cited by-同舟云学术

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Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers

Published:2009-04-01 Issue:15 Volume:106 Page:6220-6225
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Arashiro P.,Eisenberg I.,Kho A. T.,Cerqueira A. M. P.,Canovas M.,Silva H. C. A.,Pavanello R. C. M.,Verjovski-Almeida S.,Kunkel L. M.,Zatz M.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference45 articles.

1. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4

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

3. On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy

4. Psychopathological and emotional deficits in myotonic dystrophy

5. Psychiatric disorders appear equally in patients with myotonic dystrophy, facioscapulohumeral dystrophy, and hereditary motor and sensory neuropathy type I

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1. Facioscapulohumeral Muscular Dystrophy is Associated With Altered Myoblast Proteome Dynamics;Molecular & Cellular Proteomics;2023-08

2. Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham’s razor to its various features;Journal of Neuromuscular Diseases;2023-05-02

3. Facioscapulohumeral muscular dystrophy is associated with altered myoblast proteome dynamics;2022-12-14

4. Comprehensive multi-cohort transcriptional meta-analysis of muscle diseases identifies a signature of disease severity;Scientific Reports;2022-07-04

5. Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals;Current Neuropharmacology;2021-12-13

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