Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis. - Wikidata - wikimedia - TriplyDB

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

http://www.wikidata.org/entity/Q37366124

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The proteomic profile of hereditary inclusion body myopathy Interferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy.Activation of the ubiquitin proteasome pathway in a mouse model of inflammatory myopathy: a potential therapeutic target Expression of human amyloid precursor protein in the skeletal muscles of Drosophila results in age- and activity-dependent muscle weakness.Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics.Comparative Transcriptomic Study of Muscle Provides New Insights into the Growth Superiority of a Novel Grouper Hybrid.Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis.The molecular basis of skeletal muscle weakness in a mouse model of inflammatory myopathy Calcium dysregulation, functional calpainopathy, and endoplasmic reticulum stress in sporadic inclusion body myositis.Proteomics of skeletal muscle differentiation, neuromuscular disorders and fiber aging.Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkers Effects of type 1 diabetes mellitus on skeletal muscle: clinical observations and physiological mechanisms.Proteomic identification of biomarkers of skeletal muscle disorders.Proteomic profiling of the contractile apparatus from skeletal muscle.Amyloid deposits and inflammatory infiltrates in sporadic inclusion body myositis: the inflammatory egg comes before the degenerative chicken.Pyruvate kinase M2 and the mitochondrial ATPase Inhibitory Factor 1 provide novel biomarkers of dermatomyositis: a metabolic link to oncogenesis.Graphical modelling of molecular networks underlying sporadic inclusion body myositis.Intracellular β-amyloid accumulation leads to age-dependent progression of Ca2+ dysregulation in skeletal muscle.Proteomic profiling of muscle fibre type shifting in neuromuscular diseases.

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Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

http://www.wikidata.org/entity/Q37366124

description

article científic

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article scientifique

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artigo científico

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bilimsel makale

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scientific article published on June 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

@en

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

@nl

type

label

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

@en

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

@nl

prefLabel

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

@en

Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.

@nl

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Muscle and Nerve

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Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis

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Anthony A Amato

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Bch

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Behzad Moghadaszadeh

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Bryan Krastins

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David A Sarracino

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Jack L Pinkus

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Mohammad Salajegheh

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Remedios Nazareno

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Ronan J Walsh

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Steven A Greenberg

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P2860

Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle

Discrete nuclear structures in actively growing neuroblastoma cells are revealed by antibodies raised against phosphorylated neurofilament proteins

Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis

Human skeletal muscle-specific alpha-actinin-2 and -3 isoforms form homodimers and heterodimers in vitro and in vivo

Exponentially modified protein abundance index (emPAI) for estimation of absolute protein amount in proteomics by the number of sequenced peptides per protein

A controlled study of intravenous immunoglobulin combined with prednisone in the treatment of IBM.

Depth of proteome issues: a yeast isotope-coded affinity tag reagent study.

A local antigen-driven humoral response is present in the inflammatory myopathies.

Inclusion body myositis and myopathies.

Recognition of Alzheimer paired helical filaments by monoclonal neurofilament antibodies is due to crossreaction with tau protein

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739-753

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scholarly article

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10.1002/MUS.21230

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6

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39

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Kenneth C. Parker

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2009-06-01T00:00:00Z

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24206068

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