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Neurobiology of Aging, ISSN 0197-4580, 09/2018, Volume 69, pp. 293.e9 - 293.e11
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 | Sclerosis | 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 | Index Medicus | T-cell-restricted intracellular antigen-1
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 04/2018, Volume 64, pp. 160.e9 - 160.e12
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the progressive loss of motor neurons in the brain and spinal cord.... 
Frontotemporal dementia | Amyotrophic lateral sclerosis | TIA1 | CRITERIA | MAMMALIAN STRESS GRANULES | ALS | C9ORF72 | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | REGULATOR | DISTAL MYOPATHY | MESSENGER-RNA | EXPANSION | FTD | HEXANUCLEOTIDE REPEAT | Index Medicus
Journal Article
Autophagy, ISSN 1554-8627, 06/2014, Volume 10, Issue 6, pp. 957 - 971
Journal Article
Journal Article
Journal Article
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 01/2018, Volume 19, Issue 1-2, pp. 1 - 3
Journal Article
neurogenetics, ISSN 1364-6745, 5/2014, Volume 15, Issue 2, pp. 135 - 144
Journal Article
RNA Biology, ISSN 1547-6286, 07/2011, Volume 8, Issue 4, pp. 600 - 606
Humans have two nearly identical copies of the Survival Motor Neuron (SMN) gene: SMN1 and SMN2. The two SMN genes code for identical proteins; however, SMN2... 
Proteins | Binding | Landes | Calcium | Biology | Bioscience | Cell | Cycle | Organogenesis | Cancer | TIA1 | Splicing | SMA | SMN2 | hnRNPA1 | SMN1 | ISS-N1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-PROTEIN | SURVIVAL-MOTOR-NEURON | CRITICAL EXON | SINGLE NUCLEOTIDE | PRE-MESSENGER-RNA | MOUSE MODEL | DETERMINING GENE | EMBRYONIC LETHALITY | ANIMAL-MODEL | ANTISENSE OLIGONUCLEOTIDES | Alternative Splicing