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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2010, Volume 107, Issue 7, pp. 3169 - 3174
Journal Article
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 09/2010, Volume 69, Issue 9, pp. 918 - 929
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
Journal Article
Molecular and Cellular Neuroscience, ISSN 1044-7431, 10/2019, Volume 100, p. 103396
Genetic mutations in TAR DNA-binding protein 43 (TDP-43) cause amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Importantly, TDP-43... 
Mitochondria | Neurodegenerative diseases | Neurodegeneration | TDP-43 | Amyotrophic lateral sclerosis | Frontotemporal dementia | TDP-43 proteinopathy | Alzheimer's disease
Journal Article
Neurology, ISSN 0028-3878, 08/2015, Volume 85, Issue 8, pp. 658 - 660
Multisystem proteinopathy (MSP) is an inherited pleiotropic degenerative disorder that can affect muscle, bone, and the nervous system and was first reported... 
DISTAL MYOPATHY | INCLUSION-BODY MYOPATHY | TDP-43 | FRONTOTEMPORAL DEMENTIA | GIRDLE MUSCULAR-DYSTROPHY | OPTINEURIN | AUTOPHAGY | GRANULES | PAGET-DISEASE | CLINICAL NEUROLOGY | SQSTM1 MUTATIONS | Male | Distal Myopathies - genetics | Vacuoles - pathology | Humans | Adaptor Proteins, Signal Transducing - genetics
Journal Article
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 9/2007, Volume 114, Issue 3, pp. 221 - 229
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 03/2018, Volume 128, Issue 3, pp. 1164 - 1177
Journal Article