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Neurology, ISSN 0028-3878, 10/2015, Volume 85, Issue 15, pp. 1354 - 1355
Journal Article
Neuron, ISSN 0896-6273, 10/2011, Volume 72, Issue 2, pp. 245 - 256
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2012, Volume 44, Issue 2, pp. 200 - 205
Journal Article
Neuron, ISSN 0896-6273, 08/2017, Volume 95, Issue 4, pp. 808 - 816.e9
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are age-related neurodegenerative disorders with shared genetic etiologies and... 
low-complexity domain | liquid-liquid phase separation | TDP-43 | T cell-restricted intracellular antigen-1 | stress granules | frontotemporal dementia | amyotrophic lateral sclerosis | membrane-less organelle | frontotemporal lobar degeneration | MULTISYSTEM PROTEINOPATHY | DISTAL MYOPATHY | MESSENGER-RNA | LIQUID DROPLETS | SEQUENCING DATA | HEXANUCLEOTIDE REPEAT | DOMAINS | C9ORF72 | NEUROSCIENCES | FAMILIAL ALS | Humans | Middle Aged | Family Health | Male | Green Fluorescent Proteins - genetics | DNA-Binding Proteins - metabolism | Transfection | Time Factors | Adult | Female | T-Cell Intracellular Antigen-1 | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Stress, Physiological - physiology | Green Fluorescent Proteins - metabolism | Poly(A)-Binding Proteins - genetics | Amyotrophic Lateral Sclerosis - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | RNA-Binding Protein FUS - metabolism | Mutation - genetics | Heterogeneous Nuclear Ribonucleoprotein A1 | Microscopy, Confocal | Amyotrophic Lateral Sclerosis - pathology | Aged | HeLa Cells | Nervous system diseases | RNA | Analysis | Genetic research | Development and progression | Amyotrophic lateral sclerosis | Genetic aspects | T cells | Binding proteins | Protein binding | Dementia | Disease | Pathogenesis | Genes | Disorders | Lymphocytes T | Phase transitions | Proteins | Consortia | DNA-binding protein | Etiology | Dementia disorders | Age | Deoxyribonucleic acid--DNA | Phase transformations | Neurodegenerative diseases | Metabolism | Ribonucleic acid--RNA | Pathology | Phase separation | Mutation | Frontotemporal dementia | Dismantling | Phase transition | T-cell-restricted intracellular antigen-1
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2015, Volume 130, Issue 1, pp. 77 - 92
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 3/2014, Volume 127, Issue 3, pp. 397 - 406
Journal Article
Neurology, ISSN 0028-3878, 10/2015, Volume 85, Issue 15, pp. 1354 - 1355
Journal Article
Neurology, ISSN 0028-3878, 10/2015, Volume 85, Issue 15, pp. 1354 - 1355
Yu et al.1 investigated the association of TMEM106B variants with TAR-DNA binding protein 43 (TDP-43) pathology in elderly individuals without frontotemporal... 
CLINICAL NEUROLOGY | TDP-43 Proteinopathies - genetics | Aging - genetics | Membrane Proteins - genetics | Frontotemporal Lobar Degeneration | Humans | Genetic Loci - genetics | Female | Male | Nerve Tissue Proteins - genetics | WriteClick® Editor's Choice
Journal Article
Nature Communications, ISSN 2041-1723, 06/2016, Volume 7, Issue 1, p. 11992
Journal Article