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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2011, Volume 108, Issue 52, pp. 20881 - 20890
Amyotrophic lateral sclerosis (ALS) is a devastating and universally fatal neurodegenerative disease. Mutations in two related RNA-binding proteins, TDP-43 and... 
Aggregation | Proteins | Yeasts | Nervous system diseases | Neurodegenerative diseases | Neurons | Drosophila | Prions | Amyotrophic lateral sclerosis | Genetic mutation | WILD-TYPE | TDP-43 PROTEINOPATHY | DROSOPHILA MODEL | MULTIDISCIPLINARY SCIENCES | NEURODEGENERATION | AMYLOID PORES | TOXICITY | AMYOTROPHIC-LATERAL-SCLEROSIS | FUS MUTATIONS | FRONTOTEMPORAL LOBAR DEGENERATION | AGGREGATION | Immunohistochemistry | Protein Structure, Tertiary | RNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - metabolism | Saccharomyces cerevisiae - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Cells, Cultured | Computational Biology | Genetic Association Studies - methods | TATA-Binding Protein Associated Factors - genetics | Drosophila melanogaster - genetics | Mutation, Missense - genetics | Motor Neurons - metabolism | Animals | Spinal Cord - cytology | Yeast fungi | Gene mutations | Physiological aspects | Development and progression | Genetic aspects | Research | Binding proteins | Health aspects | Biological Sciences | amyotrophic-lateral-sclerosis; frontotemporal lobar degeneration; drosophila model; fus mutations; tdp-43 proteinopathy; amyloid pores; wild-type; toxicity; neurodegeneration; aggregation | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 4/2013, Volume 125, Issue 4, pp. 523 - 533
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2012, Volume 33, Issue 10, pp. 2527.e3 - 2527.e10
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 07/2012, Volume 21, Issue 13, pp. 2899 - 2911
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2011, Volume 108, Issue 52, p. 20881
Amyotrophic lateral sclerosis (ALS) is a devastating and universally fatal neurodegenerative disease. Mutations in two related RNA-binding proteins, TDP-43 and... 
Immunohistochemistry | Proteins | Yeast | Genes | Amyotrophic lateral sclerosis | Ribonucleic acid--RNA
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2012, Volume 33, Issue 1, pp. 210.e9 - 210.e10
Journal Article
Amyotrophic Lateral Sclerosis, ISSN 1748-2968, 09/2012, Volume 13, Issue 5, pp. 465 - 470
Journal Article
Journal Article