Molecular mechanisms and animal models of spinal muscular atrophy-Reference-Cited by-同舟云学术

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Molecular mechanisms and animal models of spinal muscular atrophy

Published:2015-04 Issue:4 Volume:1852 Page:685-692
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Edens Brittany M.,Ajroud-Driss Senda,Ma Long,Ma Yong-Chao

Funder

Schweppe Foundation, Whitehall Foundation, Families of SMA and NIH

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference100 articles.

1. Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficits;Akten;Proc. Natl. Acad. Sci. U. S. A.,2011

2. Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophy;Andreassi;Eur. J. Hum. Genet.,2004

3. Neuropathological analysis in spinal muscular atrophy type II;Araki;Acta Neuropathol.,2003

4. Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy;Avila;J. Clin. Invest.,2007

5. Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy;Baumer;PLoS Genet.,2009

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