相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Effects of overexpression of Huntingtin proteins on mitochondrial integrity
Hongmin Wang et al.
HUMAN MOLECULAR GENETICS (2009)
Investigation of Debio 025, a cyclophilin inhibitor, in the dystrophic mdx mouse, a model for Duchenne muscular dystrophy
J. Reutenauer et al.
BRITISH JOURNAL OF PHARMACOLOGY (2008)
NF-κB-dependent expression of the antiapoptotic factor c-FLIP is regulated by calpain 3, the protein involved in limb-girdle muscular dystrophy type 2A
Beatrice Benayoun et al.
FASEB JOURNAL (2008)
Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle
Yanchao Huang et al.
HUMAN MOLECULAR GENETICS (2008)
Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle
Irina Kramerova et al.
HUMAN MOLECULAR GENETICS (2008)
Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy
Douglas P. Millay et al.
NATURE MEDICINE (2008)
Alterations in inorganic phosphate in mouse hindlimb muscles during limb disuse
Neeti Pathare et al.
NMR IN BIOMEDICINE (2008)
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
Luciano Merlini et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A
Emma J. Groen et al.
BRAIN (2007)
The mitochondrial permeability transition pore and its involvement in cell death and in disease pathogenesis
Andrea Rasola et al.
APOPTOSIS (2007)
A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay
Astrid Milic et al.
NEUROMUSCULAR DISORDERS (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)
A quantitative study of bioenergetics in skeletal muscle lacking carbonic anhydrase III using 31P magnetic resonance spectroscopy
M. Liu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Pathophysiology of duchenne muscular dystrophy: Current hypotheses
Nicolas Deconinck et al.
PEDIATRIC NEUROLOGY (2007)
Regulation of the M-cadherin-β-catenin complex by calpain 3 during terminal stages of myogenic differentiation
Irina Kramerova et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Identification of putative in vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice
Niaz Cohen et al.
PROTEOMICS (2006)
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
Michael T. Lin et al.
NATURE (2006)
Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients
M Hermanová et al.
MUSCLE & NERVE (2006)
Mitochondrial localization of μ-calpain
M Garcia et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway
I Kramerova et al.
HUMAN MOLECULAR GENETICS (2005)
Inhibition of very long chain acyl-CoA dehydrogenase during cardiac ischemia
KE Mason et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2005)
LGMD2A:: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene
A Sáenz et al.
BRAIN (2005)
Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death
CP Baines et al.
NATURE (2005)
The frequency of limb girdle muscular dystrophy 2A in northeastern Italy
M Fanin et al.
NEUROMUSCULAR DISORDERS (2005)
Mitochondrial inhibition and oxidative stress: Reciprocating players in neurodegeneration
GD Zeevalk et al.
ANTIOXIDANTS & REDOX SIGNALING (2005)
Limb-girdle muscular dystrophies - from genetics to molecular pathology
SH Laval et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2004)
The nonimmunosuppressive cyclosporin analogs NIM811 and UNIL025 display nanomolar potencies on permeability transition in brain-derived mitochondria
MJ Hansson et al.
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2004)
Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro
I Kramerova et al.
HUMAN MOLECULAR GENETICS (2004)
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
WA Irwin et al.
NATURE GENETICS (2003)
Mechanisms of disease: Mitochondrial respiratory-chain diseases
S DiMauro et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)
Calpain 3 is activated through autolysis within the active site and lyses sarcomeric and sarcolemmal components
M Taveau et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
Stable expression of calpain 3 from a muscle transgene in vivo:: Immature muscle in transgenic mice suggests a role for calpain 3 in muscle maturation
MJ Spencer et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy
J Chae et al.
NEUROMUSCULAR DISORDERS (2001)
Protein ligands to HuR modulate its interaction with target mRNAs in vivo
CM Brennan et al.
JOURNAL OF CELL BIOLOGY (2000)