Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy (Q42739866)

6 November 2017

Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy (English)

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Céline Boudreau-Larivière

6 November 2017

spinal muscular atrophy

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Rashmi Kothary

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object named as

Céline Boudreau-Larivière

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author name string

Justin G Boyer

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6 November 2017

Marc-Olivier Deguise

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6 November 2017

Lyndsay M Murray

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6 November 2017

Armin Yazdani

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6 November 2017

Yves De Repentigny

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6 November 2017

Céline Boudreau-Larivière

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6 November 2017

1 April 2014

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6 November 2017

Human Molecular Genetics

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6 November 2017

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6 November 2017

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6 November 2017

4249-4259

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describes a project that uses

6 November 2017

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4103674/fullTextXML

inferred from PubMed Central ID database lookup

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Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy

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Histone deacetylase inhibition suppresses myogenin-dependent atrogene activation in spinal muscular atrophy mice

27 May 2018

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Survival motor neuron protein in motor neurons determines synaptic integrity in spinal muscular atrophy

27 May 2018

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A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology.

27 May 2018

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Histone deacetylase inhibitor trichostatin A enhances myogenesis by coordinating muscle regulatory factors and myogenic repressors

27 May 2018

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Muscles in a mouse model of spinal muscular atrophy show profound defects in neuromuscular development even in the absence of failure in neuromuscular transmission or loss of motor neurons

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Hearts of dystonia musculorum mice display normal morphological and histological features but show signs of cardiac stress

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Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?

27 May 2018

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Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice

27 May 2018

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Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect

27 May 2018

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Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy

27 May 2018

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Pax-7 up-regulation inhibits myogenesis and cell cycle progression in satellite cells: a potential mechanism for self-renewal

27 May 2018

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

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SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens.

27 May 2018

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Pax7 is required for the specification of myogenic satellite cells

27 May 2018

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The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy

27 May 2018

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A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

27 May 2018

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Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

27 May 2018

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Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy

27 May 2018

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Identification and characterization of a spinal muscular atrophy-determining gene

27 May 2018

1 reference

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Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model.

27 May 2018

1 reference

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Defective Neuromuscular Junction Organization and Postnatal Myogenesis in Mice With Severe Spinal Muscular Atrophy

16 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDU142

SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN

21 January 2018

1 reference

12 December 2020

Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III

1 reference

12 December 2020

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals

1 reference

12 December 2020

Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology

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12 December 2020

Identifiers

DOI

10.1093/HMG/DDU142

1 reference

6 November 2017

1 reference

6 November 2017

PubMed publication ID

24691550

1 reference