(Q49053200)

English

Pathological hallmarks of amyotrophic lateral sclerosis/frontotemporal lobar degeneration in transgenic mice produced with TDP-43 genomic fragments.

scientific article published on 13 July 2011

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scholarly article

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

Pathological hallmarks of amyotrophic lateral sclerosis/frontotemporal lobar degeneration in transgenic mice produced with TDP-43 genomic fragments. (English)

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

amyotrophic lateral sclerosis

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5

object named as

Guy A Rouleau

1 reference

Europe PubMed Central

18 February 2018

Jean-Pierre Julien

7

object named as

Jean-Pierre Julien

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Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

2

object named as

Daniel Phaneuf

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

1

object named as

Vivek Swarup

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Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

author name string

Christine Bareil

3

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

Janice Robertson

4

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

Jasna Kriz

6

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Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

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publication date

13 July 2011

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Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

134

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18 February 2018

http://europepmc.org/abstract/MED/21752789

Pt 9

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Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

2610-2626

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

Induction of peripherin expression in subsets of brain neurons after lesion injury or cerebral ischemia.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Late onset of motor neurons in mice overexpressing wild-type peripherin

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Proximal axonal enlargement in motor neuron disease.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Modest loss of peripheral axons, muscle atrophy and formation of brain inclusions in mice with targeted deletion of gigaxonin exon 1

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Human embryonic stem cell-derived motor neurons are sensitive to the toxic effect of glial cells carrying an ALS-causing mutation

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

TDP-43: a novel neurodegenerative proteinopathy

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

TDP-43 A315T mutation in familial motor neuron disease

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Clinicopathological correlates in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

ALS: astrocytes move in as deadly neighbors

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Rethinking ALS: the FUS about TDP-43.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Are amyotrophic lateral sclerosis patients cognitively normal?

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

A method to solubilise protein aggregates for immunoassay quantification which overcomes the neurofilament "hook" effect.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Aged APP23 mice show a delay in switching to the use of a strategy in the Barnes maze.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

A neurotoxic peripherin splice variant in a mouse model of ALS

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Selective functional, regional, and neuronal vulnerability in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Progressive motor weakness in transgenic mice expressing human TDP-43.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease.

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Characterization of neuronal intermediate filament protein expression in cervical spinal motor neurons in sporadic amyotrophic lateral sclerosis (ALS).

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

An aggregate-inducing peripherin isoform generated through intron retention is upregulated in amyotrophic lateral sclerosis and associated with disease pathology

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

TDP-43 mutation in familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWR159

21 January 2018

Identifiers

10.1093/BRAIN/AWR159

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/21752789

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