Regulation of SMN protein stability (Q28304878)

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Eric Muñoz

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Deborah Y Kwon

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Charlotte J Sumner

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Kenneth H Fischbeck

Molecular and Cellular Biology

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language of work or name

English

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publication date

March 2009

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published in

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volume

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issue

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page(s)

1107-15

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describes a project that uses

ImageQuant

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2643817/fullTextXML

inferred from PubMed Central ID database lookup

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The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

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

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SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain

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12 December 2020

Salbutamol, a beta 2-adrenoceptor agonist, increases skeletal muscle strength in young men

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Clenbuterol mimics effects of innervation on myogenic regulatory factor expression

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12 December 2020

SMN oligomerization defect correlates with spinal muscular atrophy severity

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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

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A comprehensive interaction map of the human survival of motor neuron (SMN) complex

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An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN

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Identifiers

DOI

10.1128/MCB.01262-08

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PubMed publication ID

19103745

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