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Neurology, ISSN 0028-3878, 12/2014, Volume 83, Issue 24, pp. 2239 - 2246
Journal Article
Nature, ISSN 0028-0836, 03/2013, Volume 495, Issue 7442, pp. 467 - 473
Algorithms designed to identify canonical yeast prions predict that around 250 human proteins, including several RNA-binding proteins associated with... 
RNA-BINDING PROTEINS | DROSOPHILA MODEL | TDP-43 | MULTIDISCIPLINARY SCIENCES | FRONTOTEMPORAL DEMENTIA | VCP MUTATIONS | DISEASE | AMYOTROPHIC-LATERAL-SCLEROSIS | SACCHAROMYCES-CEREVISIAE | STRESS GRANULES | MULTIPLE ALIGNMENT | Prions - genetics | Humans | Molecular Sequence Data | Osteitis Deformans - metabolism | Male | Drosophila melanogaster - genetics | Osteitis Deformans - genetics | Drosophila melanogaster - metabolism | Frontotemporal Dementia - metabolism | Muscular Dystrophies, Limb-Girdle - genetics | Myositis, Inclusion Body - pathology | Female | Inclusion Bodies - metabolism | Muscular Dystrophies, Limb-Girdle - pathology | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - genetics | Frontotemporal Dementia - pathology | RNA - metabolism | Frontotemporal Dementia - genetics | Amino Acid Sequence | Prions - metabolism | Peptide Termination Factors - genetics | Amyotrophic Lateral Sclerosis - genetics | Drosophila melanogaster - cytology | Mutant Proteins - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Mutant Proteins - metabolism | Protein Structure, Tertiary - genetics | Prions - chemistry | Saccharomyces cerevisiae Proteins - genetics | Mutation - genetics | Myositis, Inclusion Body - genetics | Peptide Termination Factors - metabolism | Amyotrophic Lateral Sclerosis - pathology | Inclusion Bodies - genetics | Osteitis Deformans - pathology | Animals | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - chemistry | Muscular Dystrophies, Limb-Girdle - metabolism | Mutant Proteins - chemistry | Amyotrophic Lateral Sclerosis - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Inclusion Bodies - pathology | Myositis, Inclusion Body - metabolism | Mice | Peptide Termination Factors - chemistry | HeLa Cells | Saccharomyces cerevisiae Proteins - chemistry | Pathology | Insects | Genomics | Genetics | Software | Genomes | Mutation | Genetic testing | Patients | Index Medicus
Journal Article
Science Translational Medicine, ISSN 1946-6234, 03/2016, Volume 8, Issue 331, pp. 331ra41 - 331ra41
Journal Article
Journal Article
Neuron, ISSN 0896-6273, 04/2013, Volume 78, Issue 1, pp. 57 - 64
Valosin-containing protein (VCP) is a highly expressed member of the type II AAA+ ATPase family. mutations are the cause of inclusion body myopathy, Paget’s... 
LIPID-PEROXIDATION | SPINAL-CORD PATHOLOGY | MOUSE MODEL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | DYSFUNCTION | BONE | NEUROSCIENCES | PAGET-DISEASE | TRANSGENIC MICE | REVEALS | RNA, Small Interfering - genetics | Humans | Middle Aged | Male | Frontotemporal Dementia - metabolism | Neurons - ultrastructure | Muscular Dystrophies, Limb-Girdle - genetics | Adenosine Triphosphate - metabolism | Membrane Potential, Mitochondrial - genetics | Muscular Dystrophies, Limb-Girdle - pathology | NAD - metabolism | Fibroblasts - metabolism | Animals, Newborn | Frontotemporal Dementia - genetics | Magnesium - metabolism | Mitochondria - pathology | Fibroblasts - pathology | Mutation - genetics | Myositis, Inclusion Body - genetics | Osteitis Deformans - pathology | Muscular Dystrophies, Limb-Girdle - metabolism | Analysis of Variance | Luminescent Proteins - genetics | Adenosine Triphosphatases - genetics | Mice | Lipid Peroxidation - genetics | RNA, Small Interfering - metabolism | Valosin Containing Protein | Osteitis Deformans - metabolism | Family Health | Cerebral Cortex - cytology | Case-Control Studies | Osteitis Deformans - genetics | Transfection | Mitochondria - genetics | Cell Cycle Proteins - genetics | Myositis, Inclusion Body - pathology | Adult | Female | Neuroblastoma - pathology | Frontotemporal Dementia - pathology | Adenosine Triphosphatases - deficiency | Mice, Inbred C57BL | Cells, Cultured | Cell Cycle Proteins - deficiency | Mitochondria - metabolism | Animals | Oxygen Consumption - genetics | Myositis, Inclusion Body - metabolism | Aged | Nervous system diseases | Neurosciences | Genes | Amyotrophic lateral sclerosis | Genetic aspects | Adenosine triphosphatase | Dementia | Proteins | Medical research | Phosphorylation | Biomedical research | Disease | Rodents | Respiration | Experiments | Patients | Index Medicus | Report
Journal Article
Journal Article
Annals of Neurology, ISSN 0364-5134, 02/2017, Volume 81, Issue 2, pp. 227 - 239
Journal Article
Brain, ISSN 0006-8950, 2012, Volume 135, Issue 4, pp. 1102 - 1114
Sporadic inclusion body myositis is a severely disabling myopathy. The design of effective treatment strategies is hampered by insufficient understanding of... 
nitric oxide | IL-1β | neuroinflammation | myositis | β-amyloid | APOPTOSIS | OXIDATIVE STRESS | ACTIVATION | PROTEIN | IDIOPATHIC INFLAMMATORY MYOPATHIES | IL-1 beta | ENDOPLASMIC-RETICULUM STRESS | NEUROSCIENCES | CLINICAL NEUROLOGY | beta-amyloid | SKELETAL-MUSCLE | DISEASE | IL-1-BETA | EXPRESSION | Interleukin-1beta - pharmacology | Humans | Muscle Cells - drug effects | Cells, Cultured | Enzyme Inhibitors - pharmacology | Muscle Cells - metabolism | Gene Expression Regulation - physiology | RNA, Messenger - metabolism | Tyrosine - analogs & derivatives | Gene Expression Regulation - drug effects | Tyrosine - metabolism | Drug Interactions | Flow Cytometry | Nitric Oxide Synthase Type II - genetics | Dactinomycin - analogs & derivatives | Amyloid beta-Peptides - metabolism | Amyloid beta-Protein Precursor - metabolism | Myositis, Inclusion Body - pathology | Myositis, Inclusion Body - metabolism | Cell Death - drug effects | Interferon-gamma - pharmacology | Nitric Oxide Synthase Type II - metabolism | Index Medicus | Abridged Index Medicus | Immunohistochemistry | Cell culture | Flow cytometry | beta -Amyloid | mRNA | Muscular dystrophy | Inclusion bodies | Interleukin 1 | Dementia disorders | Alzheimer's disease | Tyrosine | Nitration | Myotubes | Neurodegenerative diseases | Dermatomyositis | Data processing | Amyloid precursor protein | Desmin | Nitric-oxide synthase | Skeletal muscle | Stress | Myoblasts | Polymerase chain reaction | Polymyositis | Cell death | Nitric oxide | gamma -Interferon | Myositis | nitrotyrosine | Myopathy
Journal Article
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 02/2007, Volume 66, Issue 2, pp. 152 - 157
Journal Article