(Q47071494)

5 January 2018

title

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

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5 January 2018

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Fabian Feiguin

1

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Vinay K Godena

2

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Giulia Romano

3

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Andrea D'Ambrogio

4

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Raffaella Klima

5

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Francisco E Baralle

6

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language of work or name

English

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publication date

19 April 2009

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5 January 2018

published in

FEBS Letters

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volume

583

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issue

10

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page(s)

1586-1592

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

cites work

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

Clinical and pathological continuum of multisystem TDP-43 proteinopathies

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

TAR DNA-binding protein-43 in amyotrophic lateral sclerosis, frontotemporal lobar degeneration, and Alzheimer disease

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

Caspase-cleaved TAR DNA-binding protein-43 is a major pathological finding in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

Distinct morphogenetic functions of similar small GTPases: Drosophila Drac1 is involved in axonal outgrowth and myoblast fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

Extension of Drosophila lifespan by overexpression of human SOD1 in motorneurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

Antibodies to horseradish peroxidase as specific neuronal markers in Drosophila and in grasshopper embryos

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

Selected methods for the anatomical study of Drosophila embryonic and larval neuromuscular junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2009.04.019

10.1016/J.FEBSLET.2009.04.019

21 January 2018

Identifiers

DOI

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5 January 2018

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5 January 2018