Increase of nitric oxide synthases and nitrotyrosine in inclusion‐body myositis

No abstract is available for this paper.

• Publication year

  1996

• Venue

  NeuroReport

• Publication date

  1996-12-20

• Fields of study

  Medicine, Chemistry

• Identifiers
  DOI 10.1097/00001756-199612200-00031PMID 9051771
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Difference in Expression of Phosphorylated Tau Epitopes between Sporadic Inclusion‐body Myositis and Hereditary Inclusion‐body Myopathies

  1996cited by this paper
• Evidence of neuronal oxidative damage in Alzheimer's disease.

  1996cited by this paper
• Nitric oxide synthase and neuronal vulnerability in Parkinson's disease.

  1996cited by this paper
• Transfer of beta-amyloid precursor protein gene using adenovirus vector causes mitochondrial abnormalities in cultured normal human muscle.

  1996cited by this paper
• Use of anti‐neurofilament antibody to identify paired‐helical filaments in inclusion‐body myositis

  1996cited by this paper
• Mitochondrial DNA Deletions in Muscle Fibers in Inclusion Body Myositis

  1995cited by this paper
• Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy.

  1995cited by this paper
• New advances in the understanding of sporadic inclusion‐body myositis and hereditary inclusion‐body myopathies

  1995cited by this paper
• Induction of nitrotyrosine-like immunoreactivity in the lower motor neuron of amyotrophic lateral sclerosis.

  1995cited by this paper
• The role of peroxynitrite in nitric oxide-mediated toxicity.

  1995cited by this paper
• Nitric oxide regulates mitochondrial respiration and cell functions by inhibiting cytochrome oxidase

  1995cited by this paper
• Regulation of biosynthesis of nitric oxide.

  1994cited by this paper
• Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy.

  1994cited by this paper
• Nitric oxide synthase isozymes. Characterization, purification, molecular cloning, and functions.

  1994cited by this paper
• Gases as biological messengers: nitric oxide and carbon monoxide in the brain

  1994cited by this paper
• Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau.

  1994cited by this paper
• Reactions of nitric oxide, superoxide and peroxynitrite with superoxide dismutase in neurodegeneration.

  1994cited by this paper
• Prion protein is abnormally accumulated in inclusion‐body myositis

  1993cited by this paper
• beta-Amyloid 25-35 activates nitric oxide synthase in a neuronal clone.

  1993cited by this paper
• Cloned human brain nitric oxide synthase is highly expressed in skeletal muscle

  1993cited by this paper
• beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle.

  1993cited by this paper
• Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis.

  1992cited by this paper
• Muscle biopsies in neuromuscular diseases.

  1967cited by this paper

• Molecular Mechanisms and Therapeutic Potential of DJ‐1 in Skeletal Muscle Homeostasis and Disease

  2026cites this paper
• Sporadic Inclusion Body Myositis at the Crossroads between Muscle Degeneration, Inflammation, and Aging

  2024cites this paper
• Oxidative stress, mitochondrial dysfunction, and respiratory chain enzyme defects in inflammatory myopathies.

  2023cites this paper
• Melanomacrophage Centers in Nile Tilapia (Oreochromis niloticus L.) as Biomarker for Carbamate Exposure

  2021cites this paper
• Expression of DJ-1 in Neurodegenerative Disorders.

  2017cites this paper
• Immune and myodegenerative pathomechanisms in inclusion body myositis

  2017cites this paper
• Genetic Investigations of Sporadic Inclusion Body Myositis and Myopathies with Structural Abnormalities and Protein Aggregates in Muscle

  2016cites this paper
• Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy.

  2015cites this paper
• Sodium phenylbutyrate reverses lysosomal dysfunction and decreases amyloid-β42 in an in vitro-model of inclusion-body myositis.

  2014cites this paper
• Sporadic inclusion body myositis: the genetic contributions to the pathogenesis

  2014cites this paper
• Increased expression of manganese superoxide dismutase is associated with that of nitrotyrosine in myopathies with rimmed vacuoles

  2014influential citation
• 2 Sporadic inclusion-body myositis: A degenerative muscle disease 3 associated with aging, impaired muscle protein homeostasis and

  2014cites this paper
• Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms.

  2013cites this paper
• Chaperone‐mediated autophagy components are upregulated in sporadic inclusion‐body myositis muscle fibres

  2013cites this paper
• Muscle Aging, Inclusion-Body Myositis and Myopathies: Askanas/Muscle Aging, Inclusion-Body Myositis and Myopathies

  2012cites this paper
• Localization of O-GlcNAc-modified proteins in neuromuscular diseases

  2012cites this paper
• Activation of the γ-secretase complex and presence of γ-secretase-activating protein may contribute to Aβ42 production in sporadic inclusion-body myositis muscle fibers.

  2012cites this paper
• Pathogenic Considerations in Sporadic Inclusion-Body Myositis, a Degenerative Muscle Disease Associated With Aging and Abnormalities of Myoproteostasis

  2012cites this paper
• Sporadic inclusion-body myositis: conformational multifactorial ageing-related degenerative muscle disease associated with proteasomal and lysosomal inhibition, endoplasmic reticulum stress, and accumulation of amyloid-β42 oligomers and phosphorylated tau.

  2011cites this paper
• Myonuclear breakdown in sporadic inclusion body myositis is accompanied by DNA double strand breaks.

  2011cites this paper
• Pathogenesis of Sporadic Inclusion‐Body Myositis: Role of Aging and Muscle‐Fiber Degeneration, and Accumulation of the Same Proteins as in Alzheimer and Parkinson Brains

  2011cites this paper
• Decreased SIRT1 deacetylase activity in sporadic inclusion-body myositis muscle fibers.

  2010cites this paper
• Increased BACE1 mRNA and noncoding BACE1-antisense transcript in sporadic inclusion-body myositis muscle fibers--possibly caused by endoplasmic reticulum stress.

  2010cites this paper
• Theories of the Pathogenesis of Inclusion Body Myositis

  2010cites this paper
• Impaired autophagy in sporadic inclusion-body myositis and in endoplasmic reticulum stress-provoked cultured human muscle fibers.

  2010cites this paper
• Patologia molecular de les miopaties miofibril·lars

  2010cites this paper
• Inclusion Body Myositis: A Degenerative Muscle Disease Associated with Intra‐Muscle Fiber Multi‐Protein Aggregates, Proteasome Inhibition, Endoplasmic Reticulum Stress and Decreased Lysosomal Degradation

  2009cites this paper
• How citation distortions create unfounded authority : analysis of a citation network

  2009cites this paper
• p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis

  2009cites this paper
• Hereditary inclusion‐body myopathy: Clues on pathogenesis and possible therapy

  2009cites this paper
• Inclusion body myositis: old and new concepts

  2009cites this paper
• How citation distortions create unfounded authority: analysis of a citation network

  2009cites this paper
• In inclusion-body myositis muscle fibers Parkinson-associated DJ-1 is increased and oxidized.

  2008cites this paper
• Review Sporadic inclusion body myositis: a continuing puzzle

  2008cites this paper
• Possible role for nitric oxide dysregulation in critical illness myopathy

  2008cites this paper
• Sporadic inclusion body myositis: a continuing puzzle.

  2008cites this paper
• Two-dimensional gel electrophoresis in inclusion body myositis.

  2008cites this paper
• Inclusion-body myositis, a multifactorial muscle disease associated with aging: current concepts of pathogenesis

  2007cites this paper
• Oxidative Stress in Desminopathies and Myotilinopathies: A Link between Oxidative Damage and Abnormal Protein Aggregation

  2007cites this paper
• Desmin Is Oxidized and Nitrated in Affected Muscles in Myotilinopathies and Desminopathies

  2007cites this paper
• Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches.

  2007cites this paper
• Generation of Nitric Oxide in the Opossum Lower Esophageal Sphincter during Physiological Experimentation

  2006cites this paper
• Muscle‐fiber apoptosis in neuromuscular diseases

  2005cites this paper
• Molecular pathology and pathogenesis of inclusion‐body myositis

  2005influential citation
• Messenger RNA degradation may be inhibited in sporadic inclusion body myositis

  2005cites this paper
• Wtrętowe zapalenie mięśni: objawy kliniczne, diagnostyczne parametry biopsji mięśniowej i rozważania patogenetyczne

  2005cites this paper
• Apolipoprotein E and Alpha-1-Antichymotrypsin Polymorphisms in Sporadic Inclusion Body Myositis

  2004cites this paper
• Insulin‐like Growth Factor I in Inclusion‐Body Myositis and Human Muscle Cultures

  2004cites this paper
• Role of Apoptosis in Myopathies

  2003cites this paper
• Apoptosis and muscle fibre loss in neuromuscular disorders.

  2002cites this paper
• Sporadic inclusion body myositis and hereditary inclusion body myopathy.

  2002cites this paper
• Inclusion body myositis.

  2002cites this paper
• Increased Expression of the Normal Cellular Isoform of Prion Protein in Inclusion‐Body Myositis, Inflammatory Myopathies and Denervation Atrophy

  2001cites this paper
• In vivo and in vitro apoptosis of human thymocytes are associated with nitrotyrosine formation.

  2001cites this paper
• Oxides and apoptosis in inflammatory myopathies

  2001cites this paper
• Production of IL-6 by human myoblasts stimulated with Abeta: relevance in the pathogenesis of IBM.

  2001cites this paper
• Neurodegeneration-associated proteins and inflammation in sporadic inclusion-body myositis.

  2001cites this paper
• Production of IL-6 by human myoblasts stimulated with A Relevance in the pathogenesis of IBM

  2001influential citation
• Tyrosine nitration: Localisation, quantification, consequences for protein function and signal transduction

  2001cites this paper
• Is nitrotyrosine generated in human erythrocytes in circulation?

  2000cites this paper
• Paired helical filaments of inclusion-body myositis muscle contain RNA and survival motor neuron protein.

  2000cites this paper
• Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cells.

  2000cites this paper
• AlphaB-crystallin immunolocalization yields new insights into inclusion body myositis.

  2000cites this paper
• Redox factor-1 in muscle biopsies of patients with inclusion-body myositis.

  2000cites this paper
• Implications of Inducible Nitric Oxide Synthase Expression and Enzyme Activity

  2000cites this paper
• &agr;B‐Crystallin immunolocalization yields new insights into inclusion body myositis

  2000cites this paper
• Nitric oxide production is increased in patients with inflammatory myositis.

  1999cites this paper
• Inclusion body myositis.

  1999cites this paper
• Biological tyrosine nitration: a pathophysiological function of nitric oxide and reactive oxygen species.

  1998cites this paper
• Sporadic inclusion-body myositis and its similarities to Alzheimer disease brain. Recent approaches to diagnosis and pathogenesis, and relation to aging.

  1998cites this paper
• Immunolocalization of transcription factor NF-kappaB in inclusion-body myositis muscle and at normal human neuromuscular junctions.

  1998cites this paper
• Nitric oxide-induced oxidative stress in autosomal recessive and dominant inclusion-body myopathies.

  1998cites this paper
• Inducible nitric oxide synthase in human diseases

  1998cites this paper
• Cell death and oxidative damage in inflammatory myopathies.

  1998cites this paper
• Fourteen Newly Recognized Proteins at the Human Neuromuscular Junctions‐and Their Nonjunctional Accumulation in Inclusion‐Body Myositisa a

  1998cites this paper
• Immunolocalization of transcription factor NF-κB in inclusion-body myositis muscle and at normal human neuromuscular junctions

  1998cites this paper
• Immunohistochemical detection of nitrotyrosine in postischemic cerebral cortex in gerbil.

  1997cites this paper
• Immunolocalization of nitric oxide synthases at the postsynaptic domain of human and rat neuromuscular junctions--light and electron microscopic studies.

  1997cites this paper
• What nitrates tyrosine? Is nitrotyrosine specific as a biomarker of peroxynitrite formation in vivo?

  1997cites this paper
• Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms

  year unknowncites this paper