RNA Misprocessing in C9orf72-Linked Neurodegeneration.

about

Patient-Derived iPSCs and iNs-Shedding New Light on the Cellular Etiology of Neurodegenerative Diseases.Control of CNS functions by RNA-binding proteins in neurological diseases

P2860

Q55220858-97DC6299-DDA6-43CA-95D0-CDB9E57754F3 Q58566969-F63F71B9-7127-4291-8BD5-89740F55BCAD

P2860

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

Item

http://www.wikidata.org/entity/Q39458329

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

@en

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

@nl

type

Item

label

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

@en

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

@nl

prefLabel

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

@en

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

@nl

P1476

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

@en

P2093

Holly V Barker

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

Michael Niblock

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

P2860

The nuclear-retained noncoding RNA MALAT1 regulates alternative splicing by modulating SR splicing factor phosphorylation

Chtop is a component of the dynamic TREX mRNA export complex

An architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspeckles

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

hnRNP H is a component of a splicing enhancer complex that activates a c-src alternative exon in neuronal cells

A large-scale analysis of mRNA polyadenylation of human and mouse genes

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

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS

Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

P304

195

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

P31

scholarly article

P356

10.3389/FNCEL.2017.00195

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

P478

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

P50

Jean-Marc Gallo

Younbok Lee

Christopher E Shaw

P577

2017-07-11T00:00:00Z

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

P698

28744202

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

P932

5504096

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

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

about

P2860

P2860

RNA Misprocessing in C9orf72-Linked Neurodegeneration.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932