| scholarly article | Q13442814 |
| P2093 | author name string | Hitoshi Takahashi | |
| Yasuko Toyoshima | |||
| P2860 | cites work | Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS | Q24297462 |
| Conjoint pathologic cascades mediated by ALS/FTLD-U linked RNA-binding proteins TDP-43 and FUS | Q24634807 | ||
| TDP-43 aggregation in neurodegeneration: are stress granules the key? | Q27692111 | ||
| Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis | Q28131672 | ||
| TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis | Q28270779 | ||
| TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis | Q29615597 | ||
| Ubiquitinated filamentous inclusions in cerebellar dentate nucleus neurons in dentatorubral-pallidoluysian atrophy contain expanded polyglutamine stretches | Q33906927 | ||
| Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy | Q33984304 | ||
| Pathology of CAG repeat diseases | Q34158005 | ||
| The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease. | Q34263380 | ||
| Roles of ataxin-2 in pathological cascades mediated by TAR DNA-binding protein 43 (TDP-43) and Fused in Sarcoma (FUS) | Q34304833 | ||
| Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease | Q36115656 | ||
| Distinct TDP-43 pathology in ALS patients with ataxin 2 intermediate-length polyQ expansions | Q36528554 | ||
| Coexistence of Huntington's disease and amyotrophic lateral sclerosis: a clinicopathologic study | Q36534978 | ||
| Concomitant TAR-DNA-binding protein 43 pathology is present in Alzheimer disease and corticobasal degeneration but not in other tauopathies | Q36860214 | ||
| TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease | Q37179756 | ||
| Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype. | Q37425165 | ||
| Colocalization of transactivation-responsive DNA-binding protein 43 and huntingtin in inclusions of Huntington disease | Q45291590 | ||
| The RNA-binding protein FUS/TLS is a common aggregate-interacting protein in polyglutamine diseases | Q45295489 | ||
| Concurrence of TDP-43, tau and alpha-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies | Q46396965 | ||
| TDP-43 mutation in familial amyotrophic lateral sclerosis | Q46625104 | ||
| Effect of topographical distribution of α-synuclein pathology on TDP-43 accumulation in Lewy body disease. | Q47608338 | ||
| Regional distribution of TDP-43 inclusions in Alzheimer disease (AD) brains: their relation to AD common pathology | Q47861971 | ||
| Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases | Q48095281 | ||
| RNA-binding proteins in neurological disease | Q48478890 | ||
| Selective occurrence of TDP-43-immunoreactive inclusions in the lower motor neurons in Machado-Joseph disease | Q48570252 | ||
| TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype | Q48864196 | ||
| Spinocerebellar ataxia type 2 (SCA2) is associated with TDP-43 pathology | Q48955730 | ||
| Phosphorylated TDP-43 in Alzheimer's disease and dementia with Lewy bodies. | Q53299106 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 77-82 | |
| P577 | publication date | 2013-07-29 | |
| P1433 | published in | Neuropathology | Q15761930 |
| P1476 | title | TDP-43 pathology in polyglutamine diseases: with reference to amyotrphic lateral sclerosis | |
| P478 | volume | 34 |
| Q30418368 | Antipurinergic therapy corrects the autism-like features in the Fragile X (Fmr1 knockout) mouse model. |
| Q48111333 | Cardiac Arrest Alters Regional Ubiquitin Levels in Association with the Blood-Brain Barrier Breakdown and Neuronal Damages in the Porcine Brain |
| Q58712192 | Distinct multilevel misregulations of Parkin and PINK1 revealed in cell and animal models of TDP-43 proteinopathy |
| Q33902853 | Elimination of undifferentiated human embryonic stem cells by cardiac glycosides |
| Q36594209 | GGGGCC microsatellite RNA is neuritically localized, induces branching defects, and perturbs transport granule function |
| Q26773168 | Golgi Fragmentation in ALS Motor Neurons. New Mechanisms Targeting Microtubules, Tethers, and Transport Vesicles |
| Q47693846 | The roles of intrinsic disorder-based liquid-liquid phase transitions in the "Dr. Jekyll-Mr. Hyde" behavior of proteins involved in amyotrophic lateral sclerosis and frontotemporal lobar degeneration |
| Q30635379 | YB-1 regulates stress granule formation and tumor progression by translationally activating G3BP1. |
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