4.5 Article

Reversible molecular pathology of skeletal muscle in spinal muscular atrophy

Related references

Note: Only part of the references are listed.
Review Cell Biology

The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy

James N. Sleigh et al.

DISEASE MODELS & MECHANISMS (2011)

Article Biochemistry & Molecular Biology

ApoE isoform-specific regulation of regeneration in the peripheral nervous system

Laura H. Comley et al.

HUMAN MOLECULAR GENETICS (2011)

Article Biochemistry & Molecular Biology

Increased IGF-1 in muscle modulates the phenotype of severe SMA mice

Marta Bosch-Marce et al.

HUMAN MOLECULAR GENETICS (2011)

Article Cell Biology

Modeling spinal muscular atrophy in Drosophila links Smn to FGF signaling

Anindya Sen et al.

JOURNAL OF CELL BIOLOGY (2011)

Article Clinical Neurology

Defective Neuromuscular Junction Organization and Postnatal Myogenesis in Mice With Severe Spinal Muscular Atrophy

Elisabet Dachs et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2011)

Article Biochemistry & Molecular Biology

Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy

Lyndsay M. Murray et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy

Markus Riessland et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy

Thomas M. Wishart et al.

HUMAN MOLECULAR GENETICS (2010)

Review Biochemistry & Molecular Biology

Spinal muscular atrophy: mechanisms and therapeutic strategies

Christian L. Lorson et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

MST1 Promotes Apoptosis through Phosphorylation of Histone H2AX

Weihong Wen et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2010)

Article Clinical Neurology

Using mouse cranial muscles to investigate neuromuscular pathology in vivo

L. M. Murray et al.

NEUROMUSCULAR DISORDERS (2010)

Article Anatomy & Morphology

Increased expression of decorin during the regeneration stage of mdx mouse

Shinichi Abe et al.

ANATOMICAL SCIENCE INTERNATIONAL (2009)

Article Biochemistry & Molecular Biology

Differential Expression of Sarcoplasmic and Myofibrillar Proteins of Rat Soleus Muscle during Denervation Atrophy

Yusuke Sato et al.

BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY (2009)

Article Biochemistry & Molecular Biology

VDAC2 is required for truncated BID-induced mitochondrial apoptosis by recruiting BAK to the mitochondria

Soumya Sinha Roy et al.

EMBO REPORTS (2009)

Article Clinical Neurology

The Developmental Pattern of Myotubes in Spinal Muscular Atrophy Indicates Prenatal Delay of Muscle Maturation

Rebeca Martinez-Hernandez et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2009)

Review Neurosciences

Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?

Arthur H. M. Burghes et al.

NATURE REVIEWS NEUROSCIENCE (2009)

Article Biochemistry & Molecular Biology

Requirement of voltage-dependent anion channel 2 for pro-apoptotic activity of Bax

H. Yamagata et al.

ONCOGENE (2009)

Article Biochemical Research Methods

Proteomic DIGE analysis of the mitochondria-enriched fraction from aged rat skeletal muscle

Kathleen O'Connell et al.

PROTEOMICS (2009)

Article Biochemistry & Molecular Biology

Galectin-1 expression in innervated and denervated skeletal muscle

Anna Svensson et al.

CELLULAR & MOLECULAR BIOLOGY LETTERS (2009)

Article Cell Biology

Spinal muscular atrophy: DNA fragmentation and immaturity of muscle fibers

Demetrios Stathas et al.

ACTA HISTOCHEMICA (2008)

Review Biochemistry & Molecular Biology

SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain

Michael P. Walker et al.

HUMAN MOLECULAR GENETICS (2008)

Review Medicine, General & Internal

Spinal muscular atrophy

Mitchell R. Lunn et al.

LANCET (2008)

Editorial Material Clinical Neurology

Spinal muscular atrophy: Motoneurone or muscle disease?

Gerta Vrbova

NEUROMUSCULAR DISORDERS (2008)

Article Multidisciplinary Sciences

RAS-RAF-MEK-dependent oxidative cell death involving voltage-dependent anion channels

Nicholas Yagoda et al.

NATURE (2007)

Article Clinical Neurology

Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases

Itsuro Higuchi et al.

NEUROMUSCULAR DISORDERS (2007)

Article Medicine, Research & Experimental

Differential expression profiling between the relative normal and dystrophic muscle tissues from the same LGMD patient

Yong Zhang et al.

JOURNAL OF TRANSLATIONAL MEDICINE (2006)

Article Cell Biology

Investigation of differentially expressed proteins in rat gastrocnemius muscle during denervation-reinnervation

Hualin Sun et al.

JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY (2006)

Article Biochemical Research Methods

Proteomic analyses of rat laryngeal muscle following denervation

ZB Li et al.

PROTEOMICS (2005)

Article Clinical Neurology

Natural history of denervation in SMA:: Relation to age, SMN2 copy number, and function

KJ Swoboda et al.

ANNALS OF NEUROLOGY (2005)

Article Medicine, Research & Experimental

Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patients

AS Arnold et al.

LABORATORY INVESTIGATION (2004)

Article Multidisciplinary Sciences

VDAC2 inhibits BAK activation and mitochondrial apoptosis

EHY Cheng et al.

SCIENCE (2003)

Article Biochemistry & Molecular Biology

Neuromuscular defects in a Drosophila survival motor neuron gene mutant

YB Chan et al.

HUMAN MOLECULAR GENETICS (2003)

Article Multidisciplinary Sciences

Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease

E Hockly et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)

Article Biochemistry & Molecular Biology

New aspects of calcium signaling in skeletal muscle cells: implications in Duchenne muscular dystrophy

P Gailly

BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS (2002)

Article Cell Biology

Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy

C Cifuentes-Diaz et al.

JOURNAL OF CELL BIOLOGY (2001)