Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy
Authors
Keywords
-
Journal
BMC Medicine
Volume 10, Issue 1, Pages -
Publisher
Springer Nature
Online
2012-03-07
DOI
10.1186/1741-7015-10-24
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Rho-kinase: important new therapeutic target in cardiovascular diseases
- (2011) Kimio Satoh et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Agrin triggers the clustering of raft-associated acetylcholine receptors through actin cytoskeleton reorganization
- (2011) Annie Cartaud et al. BIOLOGY OF THE CELL
- Reversible molecular pathology of skeletal muscle in spinal muscular atrophy
- (2011) Chantal A. Mutsaers et al. HUMAN MOLECULAR GENETICS
- Temporal requirement for high SMN expression in SMA mice
- (2011) T. T. Le et al. HUMAN MOLECULAR GENETICS
- The spinal muscular atrophy disease protein SMN is linked to the rho-kinase pathway via profilin
- (2011) Anna Nölle et al. HUMAN MOLECULAR GENETICS
- Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy
- (2011) K. K. Y. Ling et al. HUMAN MOLECULAR GENETICS
- A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology
- (2011) Mélissa Bowerman et al. NEUROMUSCULAR DISORDERS
- Prospects for the gene therapy of spinal muscular atrophy
- (2011) Marco A. Passini et al. TRENDS IN MOLECULAR MEDICINE
- Spinal Cord Injury: A Systematic Review of Current Treatment Options
- (2010) David W. Cadotte et al. CLINICAL ORTHOPAEDICS AND RELATED RESEARCH
- Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model
- (2010) Mélissa Bowerman et al. HUMAN MOLECULAR GENETICS
- Developing standard procedures for pre-clinical efficacy studies in mouse models of spinal muscular atrophy
- (2010) Raffaella Willmann et al. NEUROMUSCULAR DISORDERS
- Mouse Survival Motor Neuron Alleles That Mimic SMN2 Splicing and Are Inducible Rescue Embryonic Lethality Early in Development but Not Late
- (2010) Suzan M. Hammond et al. PLoS One
- Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy
- (2009) Lyndsay M. Murray et al. HUMAN MOLECULAR GENETICS
- The Developmental Pattern of Myotubes in Spinal Muscular Atrophy Indicates Prenatal Delay of Muscle Maturation
- (2009) Rebeca Martínez-Hernández et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- SMN, profilin IIa and plastin 3: A link between the deregulation of actin dynamics and SMA pathogenesis
- (2009) Mélissa Bowerman et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Multiple roles of HDAC inhibition in neurodegenerative conditions
- (2009) De-Maw Chuang et al. TRENDS IN NEUROSCIENCES
- Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy
- (2008) Shingo Kariya et al. HUMAN MOLECULAR GENETICS
- SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain
- (2008) Michael P. Walker et al. HUMAN MOLECULAR GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now