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Accumulation of transactive response DNA binding protein 43 in mild cognitive impairment and Alzheimer diseaseInside out: the role of nucleocytoplasmic transport in ALS and FTLDExpansive gene transfer in the rat CNS rapidly produces amyotrophic lateral sclerosis relevant sequelae when TDP-43 is overexpressed.Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy.Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia ContinuumDrosophila Valosin-Containing Protein is required for dendrite pruning through a regulatory role in mRNA metabolismMutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS).Olfactory epithelium amyloid-beta and paired helical filament-tau pathology in Alzheimer disease.Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models.Neuronal function and dysfunction of Drosophila dTDPDrosophila melanogaster in the study of human neurodegeneration.Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLD-U.Phosphorylation of hnRNP K by cyclin-dependent kinase 2 controls cytosolic accumulation of TDP-43.Genetics of frontotemporal lobar degenerationMotor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosis.Mapping cortical degeneration in ALS with magnetization transfer ratio and voxel-based morphometry.Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.Linking RNA Dysfunction and Neurodegeneration in Amyotrophic Lateral Sclerosis.On the development of markers for pathological TDP-43 in amyotrophic lateral sclerosis with and without dementia.Amelioration of toxicity in neuronal models of amyotrophic lateral sclerosis by hUPF1.Targeted depletion of TDP-43 expression in the spinal cord motor neurons leads to the development of amyotrophic lateral sclerosis-like phenotypes in mice.Retrotransposon activation contributes to neurodegeneration in a Drosophila TDP-43 model of ALSImmunolocalization of TAR DNA-binding protein of 43 kDa (TDP-43) in mouse seminiferous epithelium.The truncated C-terminal RNA recognition motif of TDP-43 protein plays a key role in forming proteinaceous aggregates.The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonismsStructural transformation of the amyloidogenic core region of TDP-43 protein initiates its aggregation and cytoplasmic inclusion.Exposure to environmental toxicants and pathogenesis of amyotrophic lateral sclerosis: state of the art and research perspectives.Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis.TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration.Alzheimer's pathogenesis: is there neuron-to-neuron propagation?TDP-43 autoregulation: implications for disease.Semantic dementia: a specific network-opathy.Genetic strategies to study TDP-43 in rodents and to develop preclinical therapeutics for amyotrophic lateral sclerosis.Harnessing the power of yeast to unravel the molecular basis of neurodegeneration.Targeting TDP-43 in neurodegenerative diseases.Familial semantic dementia with P301L mutation in the Tau gene.Restoration of motor defects caused by loss of Drosophila TDP-43 by expression of the voltage-gated calcium channel, Cacophony, in central neurons.How to bake a brain: yeast as a model neuron.TDP-43 mutations causing amyotrophic lateral sclerosis are associated with altered expression of RNA-binding protein hnRNP K and affect the Nrf2 antioxidant pathway.Altered Intracellular Milieu of ADAR2-Deficient Motor Neurons in Amyotrophic Lateral Sclerosis
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 09 January 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Molecular neuropathology of TDP-43 proteinopathies.
@en
Molecular neuropathology of TDP-43 proteinopathies.
@nl
type
label
Molecular neuropathology of TDP-43 proteinopathies.
@en
Molecular neuropathology of TDP-43 proteinopathies.
@nl
prefLabel
Molecular neuropathology of TDP-43 proteinopathies.
@en
Molecular neuropathology of TDP-43 proteinopathies.
@nl
P2860
P921
P356
P1476
Molecular neuropathology of TDP-43 proteinopathies.
@en
P2860
P304
P356
10.3390/IJMS10010232
P407
P5008
P577
2009-01-01T00:00:00Z
2009-01-09T00:00:00Z