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Autophagy, ISSN 1554-8635, 2014, Volume 6, Issue 3, pp. 330 - 344
Journal Article
Neuron (Cambridge, Mass.), 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. VCP mutations are the cause of inclusion body myopathy... 
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 | Report
Journal Article
Nature (London), ISSN 1476-4687, 2018, Volume 557, Issue 7706, pp. 558 - 563
Journal Article
Journal Article
Journal of cell science, ISSN 1477-9137, 2008, Volume 121, Issue 16, pp. 2731 - 2743
PML nuclear bodies (NBs) are involved in the regulation of key nuclear pathways but their biochemical function in nuclear metabolism is unknown... 
Promyelocytic leukemia | SP100 | SUMO | Nuclear body | FCS | RARα | Kineticss modeling | FRAP | Assembly | DNA-DAMAGE | PHOTOBLEACHING RECOVERY | RAR-ALPHA | CELL BIOLOGY | nuclear body | kinetics modeling | ANOMALOUS DIFFUSION | GREEN FLUORESCENT PROTEIN | promyelocytic leukemia | assembly | SITES | RAR alpha | CELL-CYCLE | HIGH-MOBILITY | P53 ACTIVITY | BODY | Oncogene Proteins, Fusion - metabolism | Autoantigens - metabolism | Transcription Factors - chemistry | Antigens, Nuclear - metabolism | Humans | Substrate Specificity | Protein Transport - physiology | Green Fluorescent Proteins - genetics | Recombinant Fusion Proteins - metabolism | Cell Nucleus - metabolism | Protein Isoforms - metabolism | Tumor Suppressor Proteins - chemistry | Tumor Suppressor Proteins - genetics | Diffusion | Nuclear Proteins - genetics | Green Fluorescent Proteins - metabolism | Tumor Suppressor Proteins - metabolism | Cells, Cultured | Nuclear Proteins - metabolism | Transcription Factors - genetics | Nuclear Proteins - chemistry | Protein Processing, Post-Translational - physiology | Transcription Factors - metabolism | Models, Biological | Protein Binding | Recombinant Fusion Proteins - genetics | SUMO-1 Protein - metabolism | HeLa Cells | Kinetics | Intranuclear Inclusion Bodies - metabolism | Promyelocytic Leukemia Protein | Protein Structure, Tertiary - physiology
Journal Article
Molecular biology of the cell, ISSN 1939-4586, 2001, Volume 12, Issue 5, pp. 1393 - 1407
.... Inclusion bodies with truncated huntingtin protein are formed at centrosomes and are surrounded by vimentin filaments... 
NEURONAL INTRANUCLEAR INCLUSIONS | IN-VITRO | POLYGLUTAMINE | CAG REPEATS | AMYLOID-LIKE FIBRILS | 14-3-3 PROTEINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE MODEL | GLUTAMINE REPEATS | MAMMALIAN-CELLS | NEURODEGENERATIVE DISEASES | CELL BIOLOGY
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 5/2017, Volume 114, Issue 20, pp. E3935 - E3943
Journal Article
Journal of Virology, ISSN 0022-538X, 08/2012, Volume 86, Issue 15, pp. 8245 - 8258
Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
VIROLOGY | RNA | RECOGNITION | MATRIX PROTEIN | CYTOPLASMIC INCLUSIONS | RIG-I | INFECTED-CELLS | IDENTIFICATION | NF-KAPPA-B | NONSTRUCTURAL PROTEINS | PROXIMITY LIGATION | Respiratory Syncytial Virus, Human - metabolism | Genome, Viral - genetics | Humans | Newcastle Disease - immunology | Respiratory Syncytial Virus Infections - metabolism | RNA, Messenger - metabolism | Viral Proteins - metabolism | Interferon-Induced Helicase, IFIH1 | Respiratory Syncytial Virus, Human - genetics | Adaptor Proteins, Signal Transducing - immunology | Interferon-beta - genetics | Newcastle disease virus - immunology | Vero Cells | DEAD Box Protein 58 | Intranuclear Inclusion Bodies - genetics | Viral Proteins - genetics | Nucleoproteins - metabolism | Respiratory Syncytial Virus, Human - immunology | Cell Line, Tumor | DEAD-box RNA Helicases - immunology | Respiratory Syncytial Virus Infections - pathology | Intranuclear Inclusion Bodies - metabolism | Newcastle Disease - genetics | RNA, Messenger - immunology | Interferon-beta - immunology | Nucleoproteins - genetics | Viral Proteins - immunology | Cercopithecus aethiops | Respiratory Syncytial Virus Infections - immunology | Newcastle Disease - metabolism | Intranuclear Inclusion Bodies - immunology | RNA, Viral - genetics | Genome, Viral - immunology | RNA, Viral - metabolism | DEAD-box RNA Helicases - metabolism | Newcastle Disease - pathology | Nucleoproteins - immunology | Intranuclear Inclusion Bodies - virology | RNA, Messenger - genetics | Newcastle disease virus - metabolism | Interferon-beta - biosynthesis | Respiratory Syncytial Virus Infections - genetics | Birds | Immunity, Innate | Intranuclear Inclusion Bodies - pathology | DEAD-box RNA Helicases - genetics | Animals | Newcastle disease virus - genetics | Adaptor Proteins, Signal Transducing - genetics | RNA, Viral - immunology | Adaptor Proteins, Signal Transducing - metabolism | Virus-Cell Interactions
Journal Article
Nature (London), ISSN 1476-4687, 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
Journal Article