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Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres

Neuropathology and applied neurobiology, 2013-12, Vol.39 (7), p.750-761

2013

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In sporadic inclusion body myositis muscle fibres TDP-43-positive inclusions are less frequent and robust than p62 inclusions, and are not associated with paired helical filaments

Neuropathology and applied neurobiology, 2011-04, Vol.37 (3), p.315-320

2011

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Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers

Neurology, 2004-09, Vol.63 (6), p.1114-1117

2004

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Transfer of β -Amyloid Precursor Protein Gene Using Adenovirus Vector Causes Mitochondrial Abnormalities in Cultured Normal Human Muscle

Proceedings of the National Academy of Sciences - PNAS, 1996-02, Vol.93 (3), p.1314-1319

1996

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New developments in hereditary inclusion body myopathies

Annals of neurology, 1997-04, Vol.41 (4), p.421-422

Askanas, Valerie

1997

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

Journal of neuropathology and experimental neurology, 2012-08, Vol.71 (8), p.680-693

2012

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Does Overexpression of βAPP in Aging Muscle Have a Pathogenic Role and a Relevance to Alzheimer's Disease?: Clues from Inclusion Body Myositis, Cultured Human Muscle, and Transgenic Mice

The American journal of pathology, 1998-12, Vol.153 (6), p.1673-1677

1998

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Myostatin precursor protein is increased and associates with amyloid-β precursor protein in inclusion-body myositis culture model

Neuropathology and applied neurobiology, 2007-04, Vol.33 (2), p.238-242

2007

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β-Amyloid precursor epitopes in muscle fibers of inclusion body myositis

Annals of neurology, 1993-10, Vol.34 (4), p.551-560

1993

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G.P.3.16 In skeletal muscle of patients with type-II fiber atrophy, myostatin (MSTN) and myostatin precursor protein (MSTN-PP) are both increased

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.787-787

2007

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G.P.13.15 In sporadic inclusion-body myositis muscle-fiber (s-IBM) cytoplasm, cytochrome C aggregates with α-synuclein and amyloid-β precursor protein (AβPP), but does not activate caspase-3

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.853-853

2007

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Myostatin and its precursor protein are increased in the skeletal muscle of patients with Type-II muscle fibre atrophy

Folia morphologica, 2008-02, Vol.67 (1), p.6-12

2008

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New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies

Current opinion in rheumatology, 1995-11, Vol.7 (6), p.486-496

1995

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Association of Active Extracellular Signal-Regulated Protein Kinase with Paired Helical Filaments of Inclusion-Body Myositis Muscle Suggests Its Role in Inclusion-Body Myositis Tau Phosphorylation

The American journal of pathology, 2000-06, Vol.156 (6), p.1835-1840

2000

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Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle

Neurology, 2002-02, Vol.58 (3), p.438-445

2002

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G.O.2 In sporadic inclusion-body myositis (s-IBM) muscle fibers, Parkinson-disease-associated DJ-1 is oxidized and might play a novel pathogenic role

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.766-767

2007

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Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis

The American journal of pathology, 1992-07, Vol.141 (1), p.31-36

1992

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Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau

The American journal of pathology, 1994-01, Vol.144 (1), p.177-187

1994

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Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy

The American journal of pathology, 1998-04, Vol.152 (4), p.889-895

1998

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Muscle-Specific Mutations Accumulate with Aging in Critical Human mtDNA Control Sites for Replication

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (7), p.4022-4027

2001

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Paired Helical Filaments of Inclusion-Body Myositis Muscle Contain RNA and Survival Motor Neuron Protein

The American journal of pathology, 2000-04, Vol.156 (4), p.1151-1155

2000

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Novel cytoplasmic immunolocalization of RNA polymerase II in inclusion-body myositis muscle

Neuroreport, 2001-07, Vol.12 (9), p.1809-1814

2001

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Inclusion-Body Myositis: Newest Concepts of Pathogenesis and Relation to Aging and Alzheimer Disease

Journal of neuropathology and experimental neurology, 2001-01, Vol.60 (1), p.1-14

2001

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New advances in inclusion-body myositis

Current opinion in rheumatology, 1993-11, Vol.5 (6), p.732-741

1993

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Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion- body myopathy

The American journal of pathology, 1994-12, Vol.145 (6), p.1280-1284

1994

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Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres

In sporadic inclusion body myositis muscle fibres TDP-43-positive inclusions are less frequent and robust than p62 inclusions, and are not associated with paired helical filaments

Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers

Transfer of β -Amyloid Precursor Protein Gene Using Adenovirus Vector Causes Mitochondrial Abnormalities in Cultured Normal Human Muscle

New developments in hereditary inclusion body myopathies

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

Does Overexpression of βAPP in Aging Muscle Have a Pathogenic Role and a Relevance to Alzheimer's Disease?: Clues from Inclusion Body Myositis, Cultured Human Muscle, and Transgenic Mice

Myostatin precursor protein is increased and associates with amyloid-β precursor protein in inclusion-body myositis culture model

β-Amyloid precursor epitopes in muscle fibers of inclusion body myositis

G.P.3.16 In skeletal muscle of patients with type-II fiber atrophy, myostatin (MSTN) and myostatin precursor protein (MSTN-PP) are both increased

G.P.13.15 In sporadic inclusion-body myositis muscle-fiber (s-IBM) cytoplasm, cytochrome C aggregates with α-synuclein and amyloid-β precursor protein (AβPP), but does not activate caspase-3

Myostatin and its precursor protein are increased in the skeletal muscle of patients with Type-II muscle fibre atrophy

New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies

Association of Active Extracellular Signal-Regulated Protein Kinase with Paired Helical Filaments of Inclusion-Body Myositis Muscle Suggests Its Role in Inclusion-Body Myositis Tau Phosphorylation

Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle

G.O.2 In sporadic inclusion-body myositis (s-IBM) muscle fibers, Parkinson-disease-associated DJ-1 is oxidized and might play a novel pathogenic role

Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis

Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau

Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy

Muscle-Specific Mutations Accumulate with Aging in Critical Human mtDNA Control Sites for Replication

Paired Helical Filaments of Inclusion-Body Myositis Muscle Contain RNA and Survival Motor Neuron Protein

Novel cytoplasmic immunolocalization of RNA polymerase II in inclusion-body myositis muscle

Inclusion-Body Myositis: Newest Concepts of Pathogenesis and Relation to Aging and Alzheimer Disease

New advances in inclusion-body myositis

Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion- body myopathy

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