Inclusion-body myositis and myopathies: different etiologies, possibly similar pathogenic mechanisms

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2002 • 2,424 citations

Cellular Defenses against Unfolded Proteins

2001 • 979 citations

Intraneuronal Aβ42 Accumulation in Human Brain

2000 • 955 citations

The cell biology of β-amyloid precursor protein and presenilin in Alzheimer's disease

1998 • 845 citations

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

2001 • 507 citations

The Unfolding Tale of the Unfolded Protein Response

2001 • 398 citations

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1999 • 362 citations

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1999 • 326 citations

UDP-GlcNAc 2-Epimerase: A Regulator of Cell Surface Sialylation

1999 • 313 citations

Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication

2001 • 273 citations

Modulation of β-Amyloid Precursor Protein Processing by the Low Density Lipoprotein Receptor-related Protein (LRP)

2000 • 256 citations

Specificity in intracellular protein aggregation and inclusion body formation

2001 • 230 citations

Inclusion body myositis

2011 • 220 citations

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1997 • 218 citations

A Bifunctional Enzyme Catalyzes the First Two Steps inN-Acetylneuraminic Acid Biosynthesis of Rat Liver

1997 • 215 citations

Inflammation in dysferlin myopathy: Immunohistochemical characterization of 13 patients

2001 • 198 citations

Lipid Binding to Amyloid β‐Peptide Aggregates: Preferential Binding of Cholesterol as Compared with Phosphatidylcholine and Fatty Acids

1997 • 178 citations

Key Factors in Alzheimer's Disease: β‐amyloid Precursor Protein Processing, Metabolism and Intraneuronal Transport

2001 • 176 citations

Autosomal dominant myopathy: Missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene

2000 • 154 citations

Transfer of beta-amyloid precursor protein gene using adenovirus vector causes mitochondrial abnormalities in cultured normal human muscle.

1996 • 142 citations

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

2001 • 141 citations

Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE)

2002 • 114 citations

Inclusion body myositis-like phenotype induced by transgenic overexpression of βAPP in skeletal muscle

2002 • 103 citations

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

1995 • 98 citations

Amyloid-β Deposition in Skeletal Muscle of Transgenic Mice

1998 • 88 citations

New advances in inclusion-body myositis

1993 • 80 citations

Metabolic selection of glycosylation defects in human cells

2001 • 70 citations

Transgenic Mice Over-Expressing the C-99 Fragment of βPP with an α-Secretase Site Mutation Develop a Myopathy Similar to Human Inclusion Body Myositis

1998 • 66 citations

Analysis of N‐glycans of pathological tau: possible occurrence of aberrant processing of tau in Alzheimer's disease

2001 • 66 citations

Primary structure and expression analysis of humanUDP‐N‐acetyl‐glucosamine‐2‐epimerase/N‐acetylmannosamine kinase,the bifunctional enzyme in neuraminic acid biosynthesis¹

1999 • 64 citations

Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age

2002 • 63 citations

βAPP gene transfer into cultured human muscle induces inclusion-body myositis aspects

1997 • 60 citations

Inflammatory muscle diseases

2001 • 58 citations

Familial inclusion body myositis

1992 • 57 citations

The molecular and cellular pathology of inflammatory muscle diseases

2001 • 51 citations

Facioscapulohumeral muscular dystrophy

1999 • 50 citations

Impaired innervation of cultured human muscle overexpressing βAPP experimentally and genetically

1998 • 48 citations

Apolipoprotein E and apolipoprotein E messenger RNA in muscle of inclusion body myositis and myopathies

1996 • 44 citations

Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle

2002 • 41 citations

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

2000 • 40 citations

Partial laminin ?2 chain deficiency in a patient with myopathy resembling inclusion body myositis

2000 • 30 citations

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

2000 • 29 citations

Inclusion body myositis: genetic factors, aberrant protein expression, and autoimmunity

2001 • 23 citations

Cyclin-dependent kinase 5 colocalizes with phosphorylated tau in human inclusion-body myositis paired-helical filaments and may play a role in tau phosphorylation

2000 • 22 citations

Hereditary inclusion body myopathies

1998 • 14 citations

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

2001 • 6 citations