Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases. (Q37838730)

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22 January 2020

review article

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title

Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases (English)

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22 January 2020

3

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22 January 2020

Chiara Mozzetta

5

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22 January 2020

Pier Lorenzo Puri

6

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22 January 2020

author name string

Silvia Consalvi

1

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22 January 2020

Valentina Saccone

2

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22 January 2020

Giulia Minetti

4

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language of work or name

English

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publication date

7 February 2011

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22 January 2020

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22 January 2020

volume

17

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issue

5-6

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22 January 2020

page(s)

457-465

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HDAC inhibition in rheumatoid arthritis and juvenile idiopathic arthritis

22 January 2020

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HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment

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Long-term enhancement of skeletal muscle mass and strength by single gene administration of myostatin inhibitors

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An intragenic MEF2-dependent enhancer directs muscle-specific expression of microRNAs 1 and 133

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Regulation of skeletal myogenesis by association of the MEF2 transcription factor with class II histone deacetylases

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Acetylation of MyoD directed by PCAF is necessary for the execution of the muscle program

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28 September 2017

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Deacetylase inhibitors increase muscle cell size by promoting myoblast recruitment and fusion through induction of follistatin

23 June 2018

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Selective control of Pax7 expression by TNF-activated p38α/polycomb repressive complex 2 (PRC2) signaling during muscle satellite cell differentiation.

23 June 2018

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1 September 2018

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Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle

1 September 2018

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Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis

1 September 2018

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Histone deacetylase inhibition accelerates the early events of stem cell differentiation: transcriptomic and epigenetic analysis

1 September 2018

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1 September 2018

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Functional improvement of dystrophic muscle by myostatin blockade.

1 September 2018

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1 September 2018

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The meso-angioblast: a multipotent, self-renewing cell that originates from the dorsal aorta and differentiates into most mesodermal tissues.

1 September 2018

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Dystrophin expression in the mdx mouse restored by stem cell transplantation.

1 September 2018

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Muscle regeneration by bone marrow-derived myogenic progenitors

1 September 2018

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Human reserve pluripotent mesenchymal stem cells are present in the connective tissues of skeletal muscle and dermis derived from fetal, adult, and geriatric donors

1 September 2018

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Identification and characterization of a non-satellite cell muscle resident progenitor during postnatal development

31 March 2020

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Tipping the scale: muscle versus fat

31 March 2020

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Myostatin propeptide-mediated amelioration of dystrophic pathophysiology

31 March 2020

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MicroRNAs Involved in Molecular Circuitries Relevant for the Duchenne Muscular Dystrophy Pathogenesis Are Controlled by the Dystrophin/nNOS Pathway

31 March 2020

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Sizing up muscular dystrophy

31 March 2020

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https://api.crossref.org/works/10.2119%2FMOLMED.2011.00049

Nanog and Oct4 associate with unique transcriptional repression complexes in embryonic stem cells

31 March 2020

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10.2119/MOLMED.2011.00049

31 March 2020

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21308150%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

22 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21308150%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

PubMed publication ID

21308150

1 reference