Gene expression during normal and FSHD myogenesis (Q34032716)

30 July 2017

title

Gene expression during normal and FSHD myogenesis (English)

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30 July 2017

Gregory E Crawford

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30 July 2017

Rabi Tawil

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30 July 2017

Koji Tsumagari

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30 July 2017

Shao-Chi Chang

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30 July 2017

Michelle Lacey

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30 July 2017

Carl Baribault

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30 July 2017

Sridar V Chittur

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30 July 2017

Janet Sowden

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30 July 2017

Melanie Ehrlich

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30 July 2017

publication date

27 September 2011

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30 July 2017

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30 July 2017

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30 July 2017

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describes a project that uses

30 July 2017

limma

object named as

limma

2 references

22 June 2022

https://europepmc.org/article/PMC/3204225

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

cites work

Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns

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DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo

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Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt?

5 July 2018

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Testing the effects of FSHD candidate gene expression in vertebrate muscle development

5 July 2018

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5 July 2018

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5 July 2018

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DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2

5 July 2018

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Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level

5 July 2018

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Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD.

5 July 2018

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Klhl31 is associated with skeletal myogenesis and its expression is regulated by myogenic signals and Myf-5.

5 July 2018

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Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).

5 July 2018

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RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

5 July 2018

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Gene expression profiling in limb-girdle muscular dystrophy 2A

5 July 2018

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An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies

5 July 2018

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DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation

5 July 2018

1 reference

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

5 July 2018

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Retinoblastoma tumor suppressor protein-dependent methylation of histone H3 lysine 27 is associated with irreversible cell cycle exit

5 July 2018

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mTOR controls mitochondrial oxidative function through a YY1-PGC-1alpha transcriptional complex

5 July 2018

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DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Distinctive patterns of microRNA expression in primary muscular disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

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

5 July 2018

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Control of MyoD function during initiation of muscle differentiation by an autocrine signaling pathway activated by insulin-like growth factor-II.

5 July 2018

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Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1

5 July 2018

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MyoD and the transcriptional control of myogenesis

5 July 2018

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Mechanisms underlying the transcriptional regulation of skeletal myogenesis.

5 July 2018

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The Rho family of small GTPases: crucial regulators of skeletal myogenesis

5 July 2018

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Large-scale gene expression analysis of human skeletal myoblast differentiation.

5 July 2018

1 reference

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Gene expression profiling of human satellite cells during muscular aging using cDNA arrays

5 July 2018

1 reference

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Glucocorticoids regulate mRNA levels for subunits of the 19 S regulatory complex of the 26 S proteasome in fast-twitch skeletal muscles.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Transcriptional profiling and regulation of the extracellular matrix during muscle regeneration

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Induction of epithelial cell death including apoptosis by enteropathogenic Escherichia coli expressing bundle-forming pili

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facioscapulo human muscular dystrophy. A potential target for pharmacological treatment?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Among translational effectors, p70S6k is uniquely sensitive to inhibition by glucocorticoids

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Glucocorticoids and muscle catabolism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Specific increase in p85alpha expression in response to dexamethasone is associated with inhibition of insulin-like growth factor-I stimulated phosphatidylinositol 3-kinase activity in cultured muscle cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

MyoD1 promoter autoregulation is mediated by two proximal E-boxes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204225

Embryonic vs. adult myogenesis: challenging the 'regeneration recapitulates development' paradigm.

5 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Gene expression profiling highlights defective myogenesis in DMD patients and a possible role for bone morphogenetic protein 4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Transforming growth factor-β enhances matrix metalloproteinase-2 expression and activity through AKT in fibroblasts derived from angiofibromas in patients with tuberous sclerosis complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-67

Sarcolemmal reorganization in facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

12 December 2020

RAGE-NF-kappaB pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

Facioscapulohumeral muscular dystrophy

1 reference

12 December 2020

Dexamethasone effects on myoblast proliferation and differentiation

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1186/1755-8794-4-67

1 reference

Dimensions Publication ID

30 July 2017

0 references

1 reference

30 July 2017

1 reference