Related references
Note: Only part of the references are listed.Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue
D. Hicks et al.
BRAIN (2009)
Bax-inhibiting peptide protects glutamate-induced cerebellar granule cell death by blocking Bax translocation
Takayuki Iriyama et al.
NEUROSCIENCE LETTERS (2009)
LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients
J. Oliveira et al.
CLINICAL GENETICS (2008)
Drug-induced readthrough of premature stop codons leads to the stabilization of laminin α2 chain mRNA in CMD myotubes
Valerie Allamand et al.
JOURNAL OF GENE MEDICINE (2008)
SIRT3 is a stress-responsive deacetylase in cardiomyocytes that protects cells from stress-mediated cell death by deacetylation of Ku70
Nagalingam R. Sundaresan et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy
Douglas P. Millay et al.
NATURE MEDICINE (2008)
Regulation of the proapoptotic factor Bax by Ku70-dependent deubiquitylation
Avigail D. Amsel et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation
Y. Li et al.
CELL DEATH AND DIFFERENTIATION (2007)
Bax-inhibiting peptides derived from Ku70 and cell-penetrating pentapeptides
J. A. Gomez et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2007)
Interaction of a cyclin E fragment with Ku70 regulates Bax-mediated apoptosis
Suparna Mazumder et al.
MOLECULAR AND CELLULAR BIOLOGY (2007)
SIRT1 promotes DNA repair activity and deacetylation of Ku70
Jaemin Jeong et al.
EXPERIMENTAL AND MOLECULAR MEDICINE (2007)
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
Alessia Angelin et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Abolishing Bax-dependent apoptosis shows beneficial effects on spinal muscular atrophy model mice
Ming S. Tsai et al.
MOLECULAR THERAPY (2006)
The role of apoptosis in neuromuscular diseases and prospects for anti-apoptosis therapy
Jeffrey B. Miller et al.
TRENDS IN MOLECULAR MEDICINE (2006)
Doxycycline attenuates and delays toxicity of the oculopharyngeal muscular dystrophy mutation in transgenic mice
JE Davies et al.
NATURE MEDICINE (2005)
Muscle-specific BCL2 expression ameliorates muscle disease in laminin α2-deficient, but not in dystrophin-deficient, mice
JA Dominov et al.
HUMAN MOLECULAR GENETICS (2005)
Acetylation of the C terminus of Ku70 by CBP and PCAF controls Bax-mediated apoptosis
HY Cohen et al.
MOLECULAR CELL (2004)
Immortalization of mouse myogenic cells can occur without loss of p16INK4a, p19ARF, or p53 and is accelerated by inactivation of Bax -: art. no. 1
JA Nowak et al.
BMC CELL BIOLOGY (2004)
Calorie restriction promotes mammalian cell survival by inducing the SIRT1 deacetylase
HY Cohen et al.
SCIENCE (2004)
Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy
M Girgenrath et al.
JOURNAL OF CLINICAL INVESTIGATION (2004)
The role of Bax-inhibiting peptide in retinal ganglion cell apoptosis after optic nerve transection
Q Qin et al.
NEUROSCIENCE LETTERS (2004)
Minocycline up-regulates Bcl-2 and protects against cell death in mitochondria
JZ Wang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
WA Irwin et al.
NATURE GENETICS (2003)
Merosin (laminin-2/4)-driven survival signaling:: Complex modulations of Bcl-2 homologs
P Laprise et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2003)
Caspase 3 activity is required for skeletal muscle differentiation
P Fernando et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Merosin-Integrin promotion of skeletal myofiber cell survival:: Differentiation state-distinct involvement of p60Fyn tyrosine kinase and p38α stress-activated MAP kinase
P Laprise et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2002)
Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for α2 chain of laminin)
V Allamand et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2002)
Unusual laminin α2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophy
G Lattanzi et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)
Share Paper
