TDP-43 dimerizes in human cells in culture. (Q39756986)

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16 January 2020

title

TDP-43 dimerizes in human cells in culture (English)

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3

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16 January 2020

author name string

Yuki Shiina

series ordinal

1

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16 January 2020

Kunimasa Arima

series ordinal

2

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16 January 2020

Jun-ichi Satoh

series ordinal

4

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16 January 2020

publication date

31 December 2009

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Cellular and Molecular Neurobiology

16 January 2020

published in

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volume

30

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issue

4

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16 January 2020

page(s)

641-652

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Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

16 January 2020

cites work

1 reference

12 December 2020

Human, Drosophila, and C.elegans TDP43: nucleic acid binding properties and splicing regulatory function

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12 December 2020

Identification of casein kinase-1 phosphorylation sites on TDP-43.

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12 December 2020

TDP-43: an emerging new player in neurodegenerative diseases

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12 December 2020

Structural determinants of the cellular localization and shuttling of TDP-43.

1 reference

12 December 2020

TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: an important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing

1 reference

12 December 2020

Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells

1 reference

12 December 2020

Mimicking aspects of frontotemporal lobar degeneration and Lou Gehrig's disease in rats via TDP-43 overexpression

1 reference

12 December 2020

Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation

1 reference

12 December 2020

Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43.

1 reference

12 December 2020

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

1 reference

12 December 2020

A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity

1 reference

12 December 2020

Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases

1 reference

12 December 2020

Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: implications for TDP-43 in the physiological response to neuronal injury

1 reference

12 December 2020

Protein microarray analysis identifies human cellular prion protein interactors

1 reference

12 December 2020

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

1 reference

12 December 2020

Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs

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12 December 2020

Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity

1 reference

12 December 2020

Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43.

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease.

1 reference

12 December 2020

Dimerization of ubiquilin is dependent upon the central region of the protein: evidence that the monomer, but not the dimer, is involved in binding presenilins

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12 December 2020

Oxidative damage of DJ-1 is linked to sporadic Parkinson and Alzheimer diseases

1 reference

12 December 2020

Structural insights into TDP-43 in nucleic-acid binding and domain interactions

1 reference

12 December 2020

TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity

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12 December 2020

Potentiation of amyotrophic lateral sclerosis (ALS)-associated TDP-43 aggregation by the proteasome-targeting factor, ubiquilin 1.

1 reference

12 December 2020

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

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12 December 2020

10.1007/S10571-009-9489-9

Identifiers

DOI

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16 January 2020

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