Latest revision | Your text |
| label / nl | label / nl |
| Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS.
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| description / ast | description / ast |
| artículu científicu espublizáu en 2011 | | artículu científicu |
| description / uk | description / uk |
| наукова стаття, опублікована в березні 2011 | | наукова стаття |
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| Property / main subject: neurotoxicity / rank | |
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| Property / main subject: neurotoxicity / reference | |
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| Property / main subject: amyotrophic lateral sclerosis / rank | |
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| Property / main subject: amyotrophic lateral sclerosis / reference | |
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| Property / main subject: toxic encephalopathy / rank | |
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| Property / main subject: toxic encephalopathy / reference | |
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| Property / cites work: The C-terminal TDP-43 fragments have a high aggregation propensity and harm neurons by a dominant-negative mechanism / rank | |
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| Property / cites work: The C-terminal TDP-43 fragments have a high aggregation propensity and harm neurons by a dominant-negative mechanism / reference | |
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| Property / cites work: Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy / rank | |
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| Property / cites work: Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy / reference | |
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| Property / cites work: Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes / rank | |
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| Property / cites work: Identification of neuronal RNA targets of TDP-43-containing ribonucleoprotein complexes / reference | |
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| Property / cites work: TDP-43 proteinopathy in familial motor neurone disease with TARDBP A315T mutation: a case report / rank | |
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| Property / cites work: TDP-43 proteinopathy in familial motor neurone disease with TARDBP A315T mutation: a case report / reference | |
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| Property / cites work: TDP-43-mediated neuron loss in vivo requires RNA-binding activity / rank | |
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| Property / cites work: TDP-43-mediated neuron loss in vivo requires RNA-binding activity / reference | |
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| Property / cites work: Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS / rank | |
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| Property / cites work: Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS / reference | |
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| Property / cites work: Neurotoxic effects of TDP-43 overexpression in C. elegans / rank | |
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| Property / cites work: Neurotoxic effects of TDP-43 overexpression in C. elegans / reference | |
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| Property / cites work: TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97. / rank | |
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| Property / cites work: TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97. / reference | |
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| Property / cites work: Transgenic rat model of neurodegeneration caused by mutation in the TDP gene. / rank | |
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| Property / cites work: Transgenic rat model of neurodegeneration caused by mutation in the TDP gene. / reference | |
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| Property / cites work: Ubiquilin modifies TDP-43 toxicity in a Drosophila model of amyotrophic lateral sclerosis (ALS). / rank | |
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| Property / cites work: Ubiquilin modifies TDP-43 toxicity in a Drosophila model of amyotrophic lateral sclerosis (ALS). / reference | |
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| Property / cites work: A Drosophila model for TDP-43 proteinopathy / rank | |
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| Property / cites work: A Drosophila model for TDP-43 proteinopathy / reference | |
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| Property / cites work: Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis / rank | |
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| Property / cites work: Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis / reference | |
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| Property / cites work: Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo / rank | |
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| Property / cites work: Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo / reference | |
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| Property / cites work: TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration / rank | |
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| Property / cites work: TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration / reference | |
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| Property / cites work: Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching / rank | |
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| Property / cites work: Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching / reference | |
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| Property / cites work: TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity / rank | |
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| Property / cites work: TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity / reference | |
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| Property / cites work: Recent advances in the genetics of amyotrophic lateral sclerosis / rank | |
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| Property / cites work: Recent advances in the genetics of amyotrophic lateral sclerosis / reference | |
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| Property / cites work: Molecular neuropathology of TDP-43 proteinopathies / rank | |
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| Property / cites work: Molecular neuropathology of TDP-43 proteinopathies / reference | |
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| Property / cites work: Rethinking ALS: the FUS about TDP-43. / rank | |
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| Property / cites work: Rethinking ALS: the FUS about TDP-43. / reference | |
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| Property / cites work: Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6 / rank | |
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| Property / cites work: Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6 / reference | |
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| Property / cites work: Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis / rank | |
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| Property / cites work: Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis / reference | |
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| Property / cites work: Genetic studies of amyotrophic lateral sclerosis: controversies and perspectives / rank | |
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| Property / cites work: Genetic studies of amyotrophic lateral sclerosis: controversies and perspectives / reference | |
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| Property / cites work: Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis / rank | |
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| Property / cites work: Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis / reference | |
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| Property / cites work: Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations / rank | |
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| Property / cites work: Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations / reference | |
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| Property / cites work: TDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander / rank | |
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| Property / cites work: TDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander / reference | |
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| Property / cites work: A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity / rank | |
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| Property / cites work: A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity / reference | |
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| Property / cites work: TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis / rank | |
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| Property / cites work: TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis / reference | |
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| Property / cites work: TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis / rank | |
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| Property / cites work: TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis / reference | |
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| Property / cites work: TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis / rank | |
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| Property / cites work: TDP-43 A315T mutation in familial motor neuron disease / rank | |
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| Property / cites work: TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor / rank | |
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| Property / cites work: TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor / reference | |
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| Property / cites work: TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis / rank | |
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| Property / cites work: TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis / reference | |
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