Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

about

Misregulation of calcium-handling proteins promotes hyperactivation of calcineurin-NFAT signaling in skeletal muscle of DM1 mice.

P2860

Q50755664-13C52A7A-A11E-4708-86D3-C0084C7EB35E

P2860

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

Item

http://www.wikidata.org/entity/Q36151477

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

@ast

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

@en

type

Item

label

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

@ast

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

@en

prefLabel

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

@ast

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

@en

P1476

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

@en

P2093

Bernard J Jasmin

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

Emma Bondy-Chorney

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

Tara E Crawford Parks

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

P2860

Mammalian staufen is a double-stranded-RNA- and tubulin-binding protein which localizes to the rough endoplasmic reticulum

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

Interaction of muscleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing

A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

Muscleblind-like 2-mediated alternative splicing in the developing brain and dysregulation in myotonic dystrophy

DNA-dependent protein kinase (DNA-PK) phosphorylates nuclear DNA helicase II/RNA helicase A and hnRNP proteins in an RNA-dependent manner

A positive modifier of spinal muscular atrophy in the SMN2 gene

A genome-wide approach identifies distinct but overlapping subsets of cellular mRNAs associated with Staufen1- and Staufen2-containing ribonucleoprotein complexes

Interaction of Staufen1 with the 5' end of mRNA facilitates translation of these RNAs

P304

e1225644

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

P31

scholarly article

P356

10.1080/21675511.2016.1225644

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

P433

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

P478

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

P50

Aymeric Ravel-Chapuis

Jocelyn Côté

P577

2016-08-19T00:00:00Z

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

P698

27695661

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

P932

5027583

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

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

about

P2860

P2860

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932