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Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscul...

Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscul...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_599aeb8b985249bcacd6dd2353dd68bb

Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy

About this item

Full title

Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy

Publisher

England: BioMed Central Ltd

Journal title

BMC medicine, 2012-03, Vol.10 (1), p.24-24, Article 24

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

Subjects

Subjects and topics

More information

Scope and Contents

Contents

Spinal muscular atrophy (SMA) is the leading genetic cause of infant death. It is caused by mutations/deletions of the survival motor neuron 1 (SMN1) gene and is typified by the loss of spinal cord motor neurons, muscular atrophy, and in severe cases, death. The SMN protein is ubiquitously expressed and various cellular- and tissue-specific functio...

Alternative Titles

Full title

Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_599aeb8b985249bcacd6dd2353dd68bb

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_599aeb8b985249bcacd6dd2353dd68bb

Other Identifiers

ISSN

1741-7015

E-ISSN

1741-7015

DOI

10.1186/1741-7015-10-24

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