TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

about

Proteinopathies and OXPHOS dysfunction in neurodegenerative diseases.Pathomechanisms of TDP-43 in neurodegeneration.

P2860

Q47372795-C3458AFF-B0AD-423B-A6D1-8BDAEE647E52 Q52730092-61B2A26B-B1B5-4666-83EE-DD74C74F8093

P2860

TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

Item

http://www.wikidata.org/entity/Q41332015

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

@en

type

Item

label

TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

@en

prefLabel

TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

@en

P1476

TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

@en

P2093

Hideaki Ishikawa

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

Hiroshi Nakayama

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

Keiichi Izumikawa

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

Koji Yamano

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

Kouki Nishikawa

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

Masato Hasegawa

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

Masato Taoka

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

Naohiro Egawa

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

Nobuhiro Takahashi

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

Takashi Nonaka

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

P2860

RNA processing in human mitochondria

Interaction of RNA with a C-terminal fragment of the amyotrophic lateral sclerosis-associated TDP43 reduces cytotoxicity

Molecular basis of UG-rich RNA recognition by the human splicing factor TDP-43

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

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9

ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy

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

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

Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy.

P2888

s41598-017-06953-y

P304

7709

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

P31

scholarly article

P356

10.1038/S41598-017-06953-Y

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

P407

English

P433

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

P478

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

P50

Richard Simpson

Harunori Yoshikawa

Haruhisa Inoue

P577

2017-08-09T00:00:00Z

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

P698

28794432

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

P932

5550480

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

TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

about

P2860

P2860

TDP-43 stabilises the processing intermediates of mitochondrial transcripts.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932