TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain. - sprookjes - yvandenbroek - TriplyDB

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

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Cytoplasmic mislocalization of RNA splicing factors and aberrant neuronal gene splicing in TDP-43 transgenic pig brain.Gene Therapy Models of Alzheimer's Disease and Other Dementias.Failure to Deliver and Translate-New Insights into RNA Dysregulation in ALS.Differential HspBP1 expression accounts for the greater vulnerability of neurons than astrocytes to misfolded proteins.Role and Therapeutic Potential of Astrocytes in Amyotrophic Lateral Sclerosis.

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TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

http://www.wikidata.org/entity/Q37708380

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 December 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

@en

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

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label

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

@en

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

@nl

prefLabel

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

@en

TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

@nl

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Human Molecular Genetics

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TDP-43 causes differential pathology in neuronal versus glial cells in the mouse brain.

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Chuan-En Wang

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Liangxue Lai

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Marta A Gaertig

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Sen Yan

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Shihua Li

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Wenjie Wei

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Xiao-Jiang Li

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P2860

Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease

Does a loss of TDP-43 function cause neurodegeneration?

Postnatal proteasome inhibition induces neurodegeneration and cognitive deficiencies in adult mice: a new model of neurodevelopment syndrome

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration.

Expression of mutant huntingtin in mouse brain astrocytes causes age-dependent neurological symptoms.

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

Drosophila TDP-43 dysfunction in glia and muscle cells cause cytological and behavioural phenotypes that characterize ALS and FTLD

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10.1093/HMG/DDT662

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