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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
Journal Article
The EMBO Journal, ISSN 0261-4189, 07/2010, Volume 29, Issue 13, pp. 2217 - 2229
Journal Article
Neuron, ISSN 0896-6273, 12/2010, Volume 68, Issue 5, pp. 857 - 864
Journal Article
Journal Article
Nature Chemical Biology, ISSN 1552-4450, 2019, Volume 15, Issue 5, pp. 444 - 444
Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 01/2018, Volume 93, Issue 1, pp. 119 - 125
Journal Article
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 06/2010, Volume 30, Issue 22, pp. 7729 - 7739
Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is a dominantly inherited degenerative disorder caused by... 
VALOSIN-CONTAINING PROTEIN | UBIQUITIN-PROTEASOME SYSTEM | INCLUSION-BODY MYOPATHY | MESSENGER-RNA | FRONTOTEMPORAL DEMENTIA | TARDBP MUTATIONS | AMYOTROPHIC-LATERAL-SCLEROSIS | BINDING PROTEIN | NEUROSCIENCES | PAGET-DISEASE | VCP DISEASE | Index Medicus
Journal Article
Autophagy, ISSN 1554-8627, 02/2010, Volume 6, Issue 2, pp. 217 - 227
VCP (VCP/p97) is a ubiquitously expressed member of the AAA + -ATPase family of chaperone-like proteins that regulates numerous cellular processes including... 
Binding | Proteins | Landes | Calcium | Bioscience | Biology | Cell | Cycle | Cancer | Organogenesis | ERAD | Ubiquitin | IBMPFD | VCP | Autophagy | p97 | CLEARANCE | COMPLEX | autophagy | ENDOPLASMIC-RETICULUM STRESS | MYOPATHY | ubiquitin | PAGET-DISEASE | HDAC6 | CELL BIOLOGY | AAA-ATPASE | DEGRADATION | PROTEASOME SYSTEM
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 06/2018, Volume 28, Issue 6, pp. 491 - 501
Over fifty missense mutations in the gene coding for valosin-containing protein (VCP) are associated with a unique autosomal dominant adult-onset progressive... 
VCP | Inclusion body myopathy | Parkinson's disease | Novel VCP mutations | p97 | Paget's disease of bone | GENE-MUTATIONS | ATPASE ACTIVITY | DEMENTIA | AMYOTROPHIC-LATERAL-SCLEROSIS | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | PAGET-DISEASE | CLINICAL NEUROLOGY | INCLUSION-BODY MYOPATHY | VCP MUTATIONS | N-DOMAIN | ENDOPLASMIC-RETICULUM
Journal Article
Brain, ISSN 0006-8950, 02/2007, Volume 130, Issue 2, pp. 381 - 393
Journal Article