(Q48766406)

15 February 2018

title

Correction of the FSHD myoblast differentiation defect by fusion with healthy myoblasts (English)

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9

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author name string

Carla Dib

1

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Yara Bou Saada

2

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Petr Dmitriev

3

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Catherine Richon

4

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Philippe Dessen

5

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Dalila Laoudj-Chenivesse

6

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Gilles Carnac

7

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Marc Lipinski

8

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publication date

27 July 2015

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Journal of Cellular Physiology

published in

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volume

231

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issue

1

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page(s)

62-71

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

cites work

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Satellite cell therapy - from mice to men

21 January 2018

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Myoblasts from affected and non-affected FSHD muscles exhibit morphological differentiation defects

21 January 2018

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A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy

21 January 2018

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Population-based incidence and prevalence of facioscapulohumeral dystrophy

21 January 2018

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The Krüppel-like factor 15 as a molecular link between myogenic factors and a chromosome 4q transcriptional enhancer implicated in facioscapulohumeral dystrophy

21 January 2018

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Simultaneous miRNA and mRNA transcriptome profiling of human myoblasts reveals a novel set of myogenic differentiation-associated miRNAs and their target genes

21 January 2018

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21 January 2018

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Inappropriate Gene Activation in FSHD

21 January 2018

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DUX4 activates germline genes, retroelements, and immune mediators: implications for facioscapulohumeral dystrophy.

21 January 2018

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The p38 MAPK signaling pathway: a major regulator of skeletal muscle development

21 January 2018

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DNA polymorphism and epigenetic marks modulate the affinity of a scaffold/matrix attachment region to the nuclear matrix

21 January 2018

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The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein

21 January 2018

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Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.

21 January 2018

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Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts

21 January 2018

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A nuclear matrix attachment site in the 4q35 locus has an enhancer-blocking activity in vivo: implications for the facio-scapulo-humeral dystrophy

21 January 2018

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Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers.

21 January 2018

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FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients

21 January 2018

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Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene

21 January 2018

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FSHD myotubes with different phenotypes exhibit distinct proteomes

21 January 2018

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DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?

21 January 2018

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Facioscapulohumeral dystrophy: the path to consensus on pathophysiology

21 January 2018

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DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy

21 January 2018

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Gene expression during normal and FSHD myogenesis

21 January 2018

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Functional muscle impairment in facioscapulohumeral muscular dystrophy is correlated with oxidative stress and mitochondrial dysfunction

21 January 2018

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Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

21 January 2018

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Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization

21 January 2018

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Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.

21 January 2018

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Increasing D4Z4 repeat copy number compromises C2C12 myoblast differentiation

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/JCP.25110

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15 February 2018

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15 February 2018