Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model.

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Analysis of the substrate recognition state of TDP-43 to single-stranded DNA using fluorescence correlation spectroscopy.

P2860

Q54972775-AD67A119-C0A1-46DD-A397-4E71E2CE038F

P2860

Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model.

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http://www.wikidata.org/entity/Q45853787

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Disulfide cross-linked multime ...... P-43A315T ALS/FTD mouse model.

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Disulfide cross-linked multime ...... P-43A315T ALS/FTD mouse model.

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type

Item

label

Disulfide cross-linked multime ...... P-43A315T ALS/FTD mouse model.

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Disulfide cross-linked multime ...... P-43A315T ALS/FTD mouse model.

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prefLabel

Disulfide cross-linked multime ...... P-43A315T ALS/FTD mouse model.

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Disulfide cross-linked multime ...... P-43A315T ALS/FTD mouse model.

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P1476

Disulfide cross-linked multime ...... DP-43A315T ALS/FTD mouse model

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P2093

Alejandra Catenaccio

http://www.w3.org/2001/XMLSchema#string

Carolina Jerez

http://www.w3.org/2001/XMLSchema#string

Claudio Hetz

http://www.w3.org/2001/XMLSchema#string

Danilo B Medinas

http://www.w3.org/2001/XMLSchema#string

Felipe A Court

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Francisca Martínez Traub

http://www.w3.org/2001/XMLSchema#string

Leslie Bargsted

http://www.w3.org/2001/XMLSchema#string

Natalia Muñoz

http://www.w3.org/2001/XMLSchema#string

Pablo Rozas

http://www.w3.org/2001/XMLSchema#string

Soledad Matus

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P2860

The genetics and neuropathology of frontotemporal lobar degeneration

Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis

State of play in amyotrophic lateral sclerosis genetics

Functional contribution of the transcription factor ATF4 to the pathogenesis of amyotrophic lateral sclerosis

Emerging mechanisms of molecular pathology in ALS

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

TDP-43 localizes in mRNA transcription and processing sites in mammalian neurons

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

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

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

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s41598-017-14399-5

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scholarly article

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10.1038/S41598-017-14399-5

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English

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http://www.w3.org/2001/XMLSchema#string

P478

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Melissa Nassif

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2017-10-27T00:00:00Z

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1092371196

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29079747

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P921

amyotrophic lateral sclerosis

P932

5660202

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Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model.

about

P2860

P2860

Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model.

description

name

type

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P1433

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