(Q51920306)

17 April 2018

title

TDP-43, a neuro-pathosignature factor, is essential for early mouse embryogenesis. (English)

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17 April 2018

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17 April 2018

author name string

Lien-Szu Wu

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17 April 2018

Wei-Cheng Cheng

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17 April 2018

Shin-Chen Hou

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17 April 2018

Yu-Ting Yan

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17 April 2018

C-K James Shen

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17 April 2018

publication date

1 January 2010

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17 April 2018

published in

Genesis

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17 April 2018

volume

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17 April 2018

issue

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17 April 2018

page(s)

56-62

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17 April 2018

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

cites work

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7 January 2021

TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression

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7 January 2021

TDP-43 overexpression enhances exon 7 inclusion during the survival of motor neuron pre-mRNA splicing

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7 January 2021

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

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7 January 2021

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

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7 January 2021

Neuromuscular defects in a Drosophila survival motor neuron gene mutant.

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7 January 2021

Mice lacking the Obox6 homeobox gene undergo normal early embryonic development and are fertile

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7 January 2021

Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior

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7 January 2021

TDP-43: a novel neurodegenerative proteinopathy

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7 January 2021

A mouse model for spinal muscular atrophy

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7 January 2021

TDP-43 depletion induces neuronal cell damage through dysregulation of Rho family GTPases

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7 January 2021

Rethinking ALS: the FUS about TDP-43.

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7 January 2021

Spinal muscular atrophy.

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7 January 2021

Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene.

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7 January 2021

Molecular neuropathology of TDP-43 proteinopathies

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7 January 2021

TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: protein misfolding diseases without amyloidosis

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7 January 2021

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

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7 January 2021

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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7 January 2021

Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

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7 January 2021

Roadmap to embryo implantation: clues from mouse models

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7 January 2021

Higher order arrangement of the eukaryotic nuclear bodies

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7 January 2021

Structural diversity and functional implications of the eukaryotic TDP gene family

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7 January 2021

TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor

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7 January 2021

TDP-43: an emerging new player in neurodegenerative diseases

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7 January 2021

Identifiers

DOI

10.1002/DVG.20584

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17 April 2018

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17 April 2018