Related references
Note: Only part of the references are listed.Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy
Justin G. Boyer et al.
HUMAN MOLECULAR GENETICS (2014)
Dissection of the Transversus Abdominis Muscle for Whole-mount Neuromuscular Junction Analysis
Lyndsay Murray et al.
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS (2014)
Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy
Justin G. Boyer et al.
SKELETAL MUSCLE (2013)
A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology
Melissa Bowerman et al.
NEUROMUSCULAR DISORDERS (2012)
Overexpression of inducible 70-kDa heat shock protein in mouse improves structural and functional recovery of skeletal muscles from atrophy
Elen H. Miyabara et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2012)
Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid
Sanne Piepers et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model
Melissa Bowerman et al.
HUMAN MOLECULAR GENETICS (2010)
Neurodevelopmental Consequences of Smn Depletion in a Mouse Model of Spinal Muscular Atrophy
Hong Liu et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2010)
Mouse Survival Motor Neuron Alleles That Mimic SMN2 Splicing and Are Inducible Rescue Embryonic Lethality Early in Development but Not Late
Suzan M. Hammond et al.
PLOS ONE (2010)
Valproic acid blocks excitability in SMA type I mouse motor neurons
Kristen Rak et al.
NEUROBIOLOGY OF DISEASE (2009)
Sustained Improvement of Spinal Muscular Atrophy Mice Treated with Trichostatin A Plus Nutrition
Heather L. Narver et al.
ANNALS OF NEUROLOGY (2008)
Histone deacetylase inhibitors up-regulate astrocyte GDNF and BDNF gene transcription and protect dopaminergic neurons
Xuefei Wu et al.
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY (2008)
Histone deacetylase inhibitors exhibit anti-inflammatory and neuroprotective effects in a rat permanent ischemic model of stroke: Multiple mechanisms of action
Hyeon Ju Kim et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2007)
Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy
Amy M. Avila et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cells
Markus Riessland et al.
HUMAN GENETICS (2006)
Endogenous α-synuclein is induced by valproic acid through histone deacetylase inhibition and participates in neuroprotection against glutamate-induced excitotoxicity
Yan Leng et al.
JOURNAL OF NEUROSCIENCE (2006)
In vitro and ex vivo evaluation of second-generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy
E Hahnen et al.
JOURNAL OF NEUROCHEMISTRY (2006)
The role of histone acetylation in SMN gene expression
LE Kernochan et al.
HUMAN MOLECULAR GENETICS (2005)
SMNΔ7, 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
TT Le et al.
HUMAN MOLECULAR GENETICS (2005)
Valproic acid increases the SMN2 protein level: a well-known drug as a potential therapy for spinal muscular atrophy
L Brichta et al.
HUMAN MOLECULAR GENETICS (2003)
Downregulation of Bcl-2 proteins in type I spinal muscular atrophy motor neurons during fetal development
C Soler-Botija et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2003)
Oxidative stress and disturbed glutamate transport in spinal muscular atrophy
M Hayashi et al.
BRAIN & DEVELOPMENT (2002)
Quantitative analyses of SMN1 and SMN2 based on real-time LightCycler PCR:: Fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy
M Feldkötter et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
The SMN genes are subject to transcriptional regulation during cellular differentiation
D Germain-Desprez et al.
GENE (2001)
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn-/- mice and results in a mouse with spinal muscular atrophy
UR Monani et al.
HUMAN MOLECULAR GENETICS (2000)
Share Paper
