4.5 Article

Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondria! function

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。
Article Biochemistry & Molecular Biology

PGC-1α overexpression via local transfection attenuates mitophagy pathway in muscle disuse atrophy

Chounghun Kang et al.

FREE RADICAL BIOLOGY AND MEDICINE (2016)

Review Medical Laboratory Technology

Discovery of new biomarkers of idiopathic inflammatory myopathy

Xin Lu et al.

CLINICA CHIMICA ACTA (2015)

Article Biochemistry & Molecular Biology

Plectin isoform P1b and P1d deficiencies differentially affect mitochondrial morphology and function in skeletal muscle

Lilli Winter et al.

HUMAN MOLECULAR GENETICS (2015)

Letter Biotechnology & Applied Microbiology

ProteomeXchange provides globally coordinated proteomics data submission and dissemination

Juan A. Vizcaino et al.

NATURE BIOTECHNOLOGY (2014)

Article Pathology

Polymyositis with cytochrome C oxidase negative fibers-a pathological and clinical challenge

Timo Siepmann et al.

ANNALS OF DIAGNOSTIC PATHOLOGY (2013)

Article Neurosciences

GNE myopathy in India

Atchayaram Nalini et al.

NEUROLOGY INDIA (2013)

Review Clinical Neurology

Mitochondrial Dysfunction in Neuromuscular Disorders

Christos D. Katsetos et al.

SEMINARS IN PEDIATRIC NEUROLOGY (2013)

Article Cell Biology

Mitochondrial Dysfunction and Defective Autophagy in the Pathogenesis of Collagen VI Muscular Dystrophies

Paolo Bernardi et al.

COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2013)

Article Rheumatology

Autoantibodies in Polymyositis and Dermatomyositis

Anna Ghirardello et al.

CURRENT RHEUMATOLOGY REPORTS (2013)

Article Physiology

Measuring mitochondrial respiration in intact single muscle fibers

Rosemary A. Schuh et al.

AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY (2012)

Article Biochemical Research Methods

Features and development of Coot

P. Emsley et al.

ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY (2010)

Article Cell Biology

Ca2+ overload and mitochondrial permeability transition pore activation in living δ-sarcoglycan-deficient cardiomyocytes

Bodvael Fraysse et al.

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2010)

Review Biochemistry & Molecular Biology

Protein Carbonylation in Skeletal Muscles: Impact on Function

Esther Barreiro et al.

ANTIOXIDANTS & REDOX SIGNALING (2010)

Article Biochemistry & Molecular Biology

Oxidative stress by monoamine oxidases is causally involved in myofiber damage in muscular dystrophy

Sara Menazza et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle

Irina Kramerova et al.

HUMAN MOLECULAR GENETICS (2009)

Article Medicine, General & Internal

Inflammatory myopathies: diagnosis and classifications

Dalia Dimitri

PRESSE MEDICALE (2009)

Article Biochemistry & Molecular Biology

Mitochondrial processes are impaired in hereditary inclusion body myopathy

Iris Eisenberg et al.

HUMAN MOLECULAR GENETICS (2008)

Article Biochemistry & Molecular Biology

Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy

Douglas P. Millay et al.

NATURE MEDICINE (2008)

Article Biochemistry & Molecular Biology

EXOG, a novel paralog of Endonuclease G in higher eukaryotes

Iwona A. Cymerman et al.

NUCLEIC ACIDS RESEARCH (2008)

Article Multidisciplinary Sciences

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)

Article Cell Biology

Activation of caspase 3, 9, 12, and Bax in masseter muscle of mdx mice during necrosis

A. Honda et al.

JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY (2007)

Article Physiology

Dynamic responses of the glutathione system to acute oxidative stress in dystrophic mouse (mdx) muscles

Roy W. R. Dudley et al.

AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY (2006)

Article Clinical Neurology

Mitochondrial abnormalities in inclusion-body myositis

A Oldfors et al.

NEUROLOGY (2006)

Article Clinical Neurology

Mitochondrial respiratory chain dysfunction in various neuromuscular diseases

S Jongpiputvanich et al.

JOURNAL OF CLINICAL NEUROSCIENCE (2005)

Article Biochemistry & Molecular Biology

Oxidative post-translational modification of tryptophan residues in cardiac mitochondrial proteins

SW Taylor et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2003)

Article Biotechnology & Applied Microbiology

A systematic approach to modeling, capturing, and disseminating proteomics experimental data

CF Taylor et al.

NATURE BIOTECHNOLOGY (2003)

Article Biology

Induction of oxidative stress in Rana ridibunda during recovery from winter hibernation

TV Bagnyukova et al.

JOURNAL OF THERMAL BIOLOGY (2003)

Review Clinical Neurology

Apoptosis and muscle fibre loss in neuromuscular disorders

DS Tews

NEUROMUSCULAR DISORDERS (2002)

Article Cardiac & Cardiovascular Systems

Reverse flux through cardiac NADP+-isocitrate dehydrogenase under normoxia and ischemia

B Comte et al.

AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2002)

Article Rheumatology

Mitochondrial disease mimicking polymyositis: A case report

A Corrado et al.

CLINICAL RHEUMATOLOGY (2002)

Review Respiratory System

Sleep and breathing in neuromuscular disease

SC Bourke et al.

EUROPEAN RESPIRATORY JOURNAL (2002)

Review Medicine, General & Internal

The muscular dystrophies

AEH Emery

LANCET (2002)

Review Biochemistry & Molecular Biology

Mitochondria-dependent apoptosis and cellular pH regulation

S Matsuyama et al.

CELL DEATH AND DIFFERENTIATION (2000)