(Q33939411)

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

30 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Beatrice Bodega

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Beatrice Bodega

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Elena Tenedini

5

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Francesco Ferrari

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Francesco Ferrari

4

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Sergio Ferrari

7

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author name string

Stefania Cheli

1

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Europe PubMed Central

PubMed publication ID

30 July 2017

Stephanie François

2

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Europe PubMed Central

PubMed publication ID

30 July 2017

Enrica Roncaglia

6

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Europe PubMed Central

PubMed publication ID

30 July 2017

Enrico Ginelli

8

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Europe PubMed Central

PubMed publication ID

30 July 2017

Raffaella Meneveri

9

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Europe PubMed Central

PubMed publication ID

30 July 2017

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publication date

13 June 2011

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Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

6

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Europe PubMed Central

PubMed publication ID

30 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

e20966

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Europe PubMed Central

PubMed publication ID

30 July 2017

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Creative Commons Attribution 4.0 International

13 June 2011

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April 2022 Public Data File from Crossref

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describes a project that uses

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limma

2 references

Europe PubMed Central

22 June 2022

https://europepmc.org/article/PMC/3113851

based on heuristic

inferred from PubMed Central ID database lookup

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

Clinical features of facioscapulohumeral muscular dystrophy 2.

1 reference

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5 July 2018

A unifying genetic model for facioscapulohumeral muscular dystrophy

1 reference

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5 July 2018

Proteome profile in Myotonic Dystrophy type 2 myotubes reveals dysfunction in protein processing and mitochondrial pathways

1 reference

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5 July 2018

Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats.

1 reference

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5 July 2018

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

1 reference

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5 July 2018

Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation

1 reference

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5 July 2018

Reduction of the rate of protein translation in patients with myotonic dystrophy 2

1 reference

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5 July 2018

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

1 reference

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5 July 2018

Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patients

1 reference

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5 July 2018

Caveolinopathies: from the biology of caveolin-3 to human diseases

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5 July 2018

Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113851

5 July 2018

Integrated functions of Pax3 and Pax7 in the regulation of proliferation, cell size and myogenic differentiation

1 reference

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5 July 2018

GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists

1 reference

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5 July 2018

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

1 reference

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5 July 2018

Epigenetic mechanisms of facioscapulohumeral muscular dystrophy

1 reference

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

Distinctive patterns of microRNA expression in primary muscular disorders

1 reference

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5 July 2018

Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy

1 reference

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5 July 2018

The oncogenic fusion protein Pax3-FKHR has a greater post-translational stability relative to Pax3 during early myogenesis

1 reference

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The dual effects of Cdh1/APC in myogenesis

1 reference

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Quantitative real-time RT-PCR data analysis: current concepts and the novel "gene expression's CT difference" formula

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pRb: master of differentiation. Coupling irreversible cell cycle withdrawal with induction of muscle-specific transcription.

1 reference

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The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation

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Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113851

5 July 2018

Modulation of Myoblast Fusion by Caveolin-3 in Dystrophic Skeletal Muscle Cells: Implications for Duchenne Muscular Dystrophy and Limb-Girdle Muscular Dystrophy-1C

1 reference

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5 July 2018

DAVID: Database for Annotation, Visualization, and Integrated Discovery

1 reference

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5 July 2018

Inappropriate Gene Activation in FSHD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113851

5 July 2018

HMG1 and 2: architectural DNA-binding proteins

1 reference

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How cells handle cholesterol.

1 reference

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5 July 2018

Ectopic Pax-3 activates MyoD and Myf-5 expression in embryonic mesoderm and neural tissue

1 reference

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5 July 2018

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)

1 reference

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5 July 2018

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

1 reference

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High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families

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Pax3 inhibits myogenic differentiation of cultured myoblast cells

1 reference

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

1 reference

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Pax3 is essential for skeletal myogenesis and the expression of Six1 and Eya2.

1 reference

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Diagnostic criteria for facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21695143

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Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21695143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facioscapulohumeral muscular dystrophy in the Dutch population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21695143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21695143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21695143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0020966

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

2011PLoSO...620966C

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

ResearchGate publication ID

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