(Q38314794)

2 September 2017

title

Loss and gain of FUS function impair neuromuscular synaptic transmission in a genetic model of ALS. (English)

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amyotrophic lateral sclerosis

2 September 2017

main subject

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2

Pierre Drapeau

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2 September 2017

Gary A B Armstrong

1

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2 September 2017

publication date

13 June 2013

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2 September 2017

published in

Human Molecular Genetics

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2 September 2017

volume

22

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2 September 2017

issue

21

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2 September 2017

page(s)

4282-4292

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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

2 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT278

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

21 January 2018

1 reference

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Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

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Review: neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy

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The "dying-back" phenomenon of motor neurons in ALS.

21 January 2018

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Calcium channel agonists protect against neuromuscular dysfunction in a genetic model of TDP-43 mutation in ALS.

21 January 2018

1 reference

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Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes

21 January 2018

1 reference

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Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion

21 January 2018

1 reference

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ALS mutations in FUS cause neuronal dysfunction and death in Caenorhabditis elegans by a dominant gain-of-function mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT278

FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis

21 January 2018

1 reference

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Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules

21 January 2018

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Paired motor neuron-muscle recordings in zebrafish test the receptor blockade model for shaping synaptic current.

21 January 2018

1 reference

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Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects

21 January 2018

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RNA-binding ability of FUS regulates neurodegeneration, cytoplasmic mislocalization and incorporation into stress granules associated with FUS carrying ALS-linked mutations

21 January 2018

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Neuromuscular transmission in amyotrophic lateral sclerosis.

21 January 2018

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Gender-Specific Mechanism of Synaptic Impairment and Its Prevention by GCSF in a Mouse Model of ALS.

21 January 2018

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Increased persistent Na(+) current and its effect on excitability in motoneurones cultured from mutant SOD1 mice.

21 January 2018

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Altered postnatal maturation of electrical properties in spinal motoneurons in a mouse model of amyotrophic lateral sclerosis.

21 January 2018

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Early interneuron dysfunction in ALS: insights from a mutant sod1 zebrafish model

21 January 2018

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Glutamate, excitotoxicity and amyotrophic lateral sclerosis

21 January 2018

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Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis

21 January 2018

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Links between Electrophysiological and Molecular Pathology of Amyotrophic Lateral Sclerosis

21 January 2018

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Rhythmic motor activity evoked by NMDA in the spinal zebrafish larva

21 January 2018

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A gradient in endogenous rhythmicity and oscillatory drive matches recruitment order in an axial motor pool

21 January 2018

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A genetic model of amyotrophic lateral sclerosis in zebrafish displays phenotypic hallmarks of motoneuron disease

21 January 2018

1 reference

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Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish

21 January 2018

1 reference

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Neuromuscular effects of G93A-SOD1 expression in zebrafish.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT278

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDT278

21 January 2018

Identifiers

DOI

10.1093/HMG/DDT278

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2 September 2017

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