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Neuron, ISSN 0896-6273, 01/2019, Volume 101, Issue 2, pp. 204 - 206
Journal Article
Nature Neuroscience, ISSN 1097-6256, 02/2018, Volume 21, Issue 2, pp. 228 - 239
The cytoplasmic mislocalization and aggregation of TAR DNA-binding protein-43 (TDP-43) is a common histopathological hallmark of the amyotrophic lateral... 
A315T MUTATION | REPEAT EXPANSION | MESSENGER-RNA | DROSOPHILA MODEL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | MOTOR-NEURON DISEASE | FRONTOTEMPORAL LOBAR DEGENERATION | EXPRESSION | NEUROSCIENCES | RNA-BINDING PROTEIN | C9orf72 Protein - genetics | Active Transport, Cell Nucleus - physiology | Humans | Nuclear Envelope - ultrastructure | Male | Drosophila Proteins - metabolism | Cerebral Cortex - cytology | DNA-Binding Proteins - metabolism | Frontotemporal Dementia - metabolism | Protein Aggregation, Pathological - pathology | Female | C9orf72 Protein - metabolism | Active Transport, Cell Nucleus - genetics | Neuroblastoma - pathology | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Animals, Genetically Modified | Amyotrophic Lateral Sclerosis - genetics | Drosophila | Mice, Inbred C57BL | Cells, Cultured | Nuclear Pore - genetics | DNA-Binding Proteins - genetics | Nuclear Pore - metabolism | DNA-Binding Proteins - ultrastructure | Amyotrophic Lateral Sclerosis - pathology | Animals | Larva | Amyotrophic Lateral Sclerosis - metabolism | C9orf72 Protein - ultrastructure | Embryo, Nonmammalian | Mice | Drosophila Proteins - genetics | Nuclear Envelope - pathology | Protein Aggregation, Pathological - metabolism | Fibroblasts | Amyotrophic lateral sclerosis | Research | Protein binding | Brain | Neurons | Cortex | Biotin | Ribonucleic acid--RNA | Pathology | DNA-binding protein | Nucleoporins | RNA transport | Aggregates | Stem cells | Dementia disorders | Mutation | Transport | Protein transport | Frontotemporal dementia | Pluripotency | Deoxyribonucleic acid--DNA
Journal Article
Nature, ISSN 0028-0836, 08/2012, Volume 488, Issue 7412, pp. 499 - 503
Journal Article
Science, ISSN 0036-8075, 4/2008, Volume 320, Issue 5875, pp. 524 - 527
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 11/2003, Volume 163, Issue 4, pp. 801 - 812
Spinal muscular atrophy (SMA), a common autosomal recessive form of motoneuron disease in infants and young adults, is caused by mutations in the survival... 
Growth cones | Axons | Neurites | Messenger RNA | Neurons | Heterogeneous nuclear ribonucleoproteins | Cell lines | Actins | Antibodies | PC12 cells | β-actin | RNA transport | SMN | HnRNP R | SMA | SURVIVAL | GRY-RBP | hnRNP R | PROGRESSIVE-MOTOR-NEURONOPATHY | CYTOPLASMIC LOCALIZATION | beta-actin | BINDING PROTEIN | SNRNP BIOGENESIS | SINGLE NUCLEOTIDE | CELL-DEATH | CELL BIOLOGY | MOUSE MODEL | MISSENSE MUTATION | Spinal Cord - metabolism | Spinal Cord - growth & development | Nerve Tissue Proteins - deficiency | 3' Untranslated Regions - genetics | Cell Survival - genetics | Axons - physiology | RNA-Binding Proteins | RNA, Messenger - metabolism | PC12 Cells | Actins - genetics | Cell Differentiation - genetics | Motor Neurons - cytology | Spinal Cord - cytology | Cyclic AMP Response Element-Binding Protein | Disease Models, Animal | Nerve Tissue Proteins - physiology | Survival of Motor Neuron 1 Protein | Heterogeneous-Nuclear Ribonucleoproteins - metabolism | Rats | Mice, Transgenic | SMN Complex Proteins | Nerve Tissue Proteins - genetics | Heterogeneous-Nuclear Ribonucleoproteins - genetics | Motor Neurons - metabolism | Animals | Growth Cones - metabolism | Growth Cones - ultrastructure | Mice | SMN1 gene | spinal muscular atrophy | Smn protein | Heterogeneous-nuclear ribonucleoprotein R | SMA; SMN; RNA transport; β-actin; hnRNP R
Journal Article
Molecular Neurodegeneration, ISSN 1750-1326, 2010, Volume 5, Issue 1, pp. 17 - 17
Journal Article