C-terminal short arginine/serine repeat sequence-dependent regulation of Y14 (RBM8A) localization.

about

C-terminal short arginine/serine repeat sequence-dependent regulation of Y14 (RBM8A) localization.

Item

http://www.wikidata.org/entity/Q49445321

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

C-terminal short arginine/seri ...... n of Y14 (RBM8A) localization.

@en

C-terminal short arginine/serine repeat sequence-dependent regulation of Y14

@nl

type

Item

label

C-terminal short arginine/seri ...... n of Y14 (RBM8A) localization.

@en

C-terminal short arginine/serine repeat sequence-dependent regulation of Y14

@nl

prefLabel

C-terminal short arginine/seri ...... n of Y14 (RBM8A) localization.

@en

C-terminal short arginine/serine repeat sequence-dependent regulation of Y14

@nl

P1476

C-terminal short arginine/seri ...... n of Y14 (RBM8A) localization.

@en

P2093

Takanori Tatsuno

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

Yasuhito Ishigaki

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

P2860

Human CWC22 escorts the helicase eIF4AIII to spliceosomes and promotes exon junction complex assembly

The crystal structure of the exon junction complex reveals how it maintains a stable grip on mRNA

Binding of a novel SMG-1-Upf1-eRF1-eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decay

A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Crystal structure of the human eIF4AIII-CWC22 complex shows how a DEAD-box protein is inhibited by a MIF4G domain

The exon junction core complex is locked onto RNA by inhibition of eIF4AIII ATPase activity

The nonsense-mediated decay RNA surveillance pathway

Pre-mRNA processing reaches back to transcription and ahead to translation

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.

P304

612

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

P31

scholarly article

P356

10.1038/S41598-017-18765-1

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

P577

2018-01-12T00:00:00Z

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

P698

29330450

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

P932

5766523

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