Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology (Q81340087)

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7 January 2020

title

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

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7 January 2020

3

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7 January 2020

author name string

Dina Shafey

series ordinal

1

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7 January 2020

Patrice D Côté

series ordinal

2

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7 January 2020

language of work or name

English

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publication date

10 October 2005

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Experimental Cell Research

7 January 2020

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16219305 AND SRC:MED&resulttype=core&format=json

7 January 2020

volume

311

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7 January 2020

issue

1

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7 January 2020

page(s)

49-61

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Classification of spinal muscular atrophies

7 January 2020

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Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patients.

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Constitutive muscular abnormalities in culture in spinal muscular atrophy

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Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy

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Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene

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Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding.

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A novel nuclear structure containing the survival of motor neurons protein

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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

7 January 2021

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Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model

7 January 2021

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A mouse model for spinal muscular atrophy

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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

7 January 2021

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A cell system with targeted disruption of the SMN gene: functional conservation of the SMN protein and dependence of Gemin2 on SMN.

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Muscle could be the therapeutic target in SMA treatment

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Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy

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The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

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A functional interaction between the survival motor neuron complex and RNA polymerase II

7 January 2021

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A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing

7 January 2021

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SMN tudor domain structure and its interaction with the Sm proteins

7 January 2021

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Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein

7 January 2021

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A role for polyproline motifs in the spinal muscular atrophy protein SMN. Profilins bind to and colocalize with smn in nuclear gems

7 January 2021

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Synergistic anti-apoptotic activity between Bcl-2 and SMN implicated in spinal muscular atrophy

7 January 2021

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The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1

7 January 2021

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7 January 2021

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Alternative splicing, expression, and genomic structure of the 3' region of the gene encoding the sarcolemmal-associated proteins (SLAPs) defines a novel class of coiled-coil tail-anchored membrane proteins

7 January 2021

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Regulated expression and temporal induction of the tail-anchored sarcolemmal-membrane-associated protein is critical for myoblast fusion

7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16219305 AND SRC:MED&resulttype=core&format=json

7 January 2020

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