Transcriptional profiling of differentially vulnerable motor neurons at pre-symptomatic stage in the Smn 2b/- mouse model of spinal muscular atrophy-Reference-Cited by-同舟云学术

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Transcriptional profiling of differentially vulnerable motor neurons at pre-symptomatic stage in the Smn 2b/- mouse model of spinal muscular atrophy

Published:2015-09-15 Issue:1 Volume:3 Page:
ISSN:2051-5960
Container-title:Acta Neuropathologica Communications
language:en
Short-container-title:acta neuropathol commun

Author:

Murray Lyndsay M.,Beauvais Ariane,Gibeault Sabrina,Courtney Natalie L.,Kothary Rashmi

Funder

Cure SMA (US)

Cure SMA Canada

Muscular Dystrophy Association (US)

Canadian Institutes of Health Research (CA)

Gwendolyn Strong Foundation

Fight SMA

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1186/s40478-015-0231-1

Reference60 articles.

1. Andrus BM, Blizinsky K, Vedell PT, Dennis K, Shukla PK, Schaffer DJ, Radulovic J, Churchill GA, Redei EE (2012) Gene expression patterns in the hippocampus and amygdala of endogenous depression and chronic stress models. Mol Psychiatry 17:49–61. doi: 10.1038/mp.2010.119

2. Ascenzi P, Gustincich S, Marino M (2014) Mammalian nerve globins in search of functions. IUBMB Life 66:268–276. doi: 10.1002/iub.1267

3. Baumer D, Lee S, Nicholson G, Davies JL, Parkinson NJ, Murray LM, Gillingwater TH, Ansorge O, Davies KE, Talbot K (2009) Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. PLoS Genet 5, e1000773. doi: 10.1371/journal.pgen.1000773

4. Bosch-Marce M, Wee CD, Martinez TL, Lipkes CE, Choe DW, Kong L, Van Meerbeke JP, Musaro A, Sumner CJ (2011) Increased IGF-1 in muscle modulates the phenotype of severe SMA mice. Hum Mol Genet 20:1844–1853. doi: 10.1093/hmg/ddr067

5. Bowerman M. MLM, Beauvais A., Pinheiro B., Kothary R. (2011) A critical Smn threshold in mice dictates onset of an intermediate Spinal Muscular Atrophy phenotype associated with a distinct neuromuscular junction pathology. Neuromuscul Disord. In Press

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