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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2012, Volume 109, Issue 15, pp. 5803 - 5808
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
Cerebral Cortex, ISSN 1047-3211, 07/2017, Volume 27, Issue 7, pp. 3630 - 3647
Journal Article
Biochemical Journal, ISSN 0264-6021, 04/2017, Volume 474, Issue 8, pp. 1417 - 1438
Approximately 70 human RNA-binding proteins (RBPs) contain a prion-like domain (PrLD). PrLDs are low-complexity domains that possess a similar amino acid... 
EUKARYOTIC STRESS GRANULES | MUTANT FUS PROTEINS | MULTISYSTEM PROTEINOPATHY | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHASE-TRANSITION | TARDBP MUTATIONS | HNRNP A1 | AMYOTROPHIC-LATERAL-SCLEROSIS | FRONTOTEMPORAL LOBAR DEGENERATION | HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEINS | NEURODEGENERATIVE DISEASES | Proteostasis Deficiencies - metabolism | RNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - metabolism | Humans | Prion Proteins - metabolism | DNA-Binding Proteins - metabolism | Frontotemporal Dementia - metabolism | RNA-Binding Protein FUS - chemistry | TDP-43 Proteinopathies - genetics | Protein Domains | TDP-43 Proteinopathies - pathology | Prion Proteins - chemistry | Prion Proteins - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - genetics | Frontotemporal Dementia - pathology | Calmodulin-Binding Proteins - genetics | Frontotemporal Dementia - genetics | Cytoplasmic Granules | Neurodegenerative Diseases - pathology | Amyotrophic Lateral Sclerosis - genetics | RNA-Binding Proteins - chemistry | TDP-43 Proteinopathies - metabolism | Proteostasis Deficiencies - pathology | RNA-Binding Protein FUS - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Neurodegenerative Diseases - genetics | Calmodulin-Binding Proteins - chemistry | Calmodulin-Binding Proteins - metabolism | RNA-Binding Protein FUS - metabolism | Neurodegenerative Diseases - metabolism | TATA-Binding Protein Associated Factors - chemistry | DNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - genetics | DNA-Binding Proteins - chemistry | Heterogeneous Nuclear Ribonucleoprotein A1 | Proteostasis Deficiencies - genetics | Amyotrophic Lateral Sclerosis - pathology | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - chemistry | Amyotrophic Lateral Sclerosis - metabolism | Mutation | RNA-Binding Proteins - metabolism | RNA-Binding Protein EWS
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2013, Volume 74, Issue 1, pp. 20 - 38
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2017, Volume 54, pp. 71 - 83
Journal Article
Journal Article
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 07/2016, Volume 36, Issue 29, pp. 7707 - 7717
Journal Article
Journal Article