Astrocytes expressing ALS-linked mutant FUS induce motor neuron death through release of tumor necrosis factor-alpha.

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Astrocytes expressing ALS-linked mutant FUS induce motor neuron death through release of tumor necrosis factor-alpha.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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Astrocytes expressing ALS-link ...... f tumor necrosis factor-alpha.

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Astrocytes expressing ALS-link ...... f tumor necrosis factor-alpha.

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Astrocytes expressing ALS-link ...... f tumor necrosis factor-alpha.

@en

Astrocytes expressing ALS-link ...... f tumor necrosis factor-alpha.

@nl

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Astrocytes expressing ALS-link ...... f tumor necrosis factor-alpha.

@en

Astrocytes expressing ALS-link ...... f tumor necrosis factor-alpha.

@nl

P1476

Astrocytes expressing ALS-link ...... f tumor necrosis factor-alpha.

@en

P2093

Azadeh Kia

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Davide Trotti

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Piera Pasinelli

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P2860

Tumor necrosis factor alpha: a link between neuroinflammation and excitotoxicity

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

Involvement of the pro-oncoprotein TLS (translocated in liposarcoma) in nuclear factor-kappa B p65-mediated transcription as a coactivator

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

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

Differential regulation of AMPA receptor and GABA receptor trafficking by tumor necrosis factor-alpha

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

Control of synaptic strength by glial TNFalpha

P304

1016-1033

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scholarly article

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10.1002/GLIA.23298

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P478

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Karthik Krishnamurthy

Kevin McAvoy

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2018-01-30T00:00:00Z

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P698

29380416

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P921

amyotrophic lateral sclerosis

astrocyte

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5873384

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