The role of the unfolded protein response in myelination

about

The role of the unfolded protein response in myelination

Item

http://www.wikidata.org/entity/Q36790795

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

The role of the unfolded protein response in myelination

@ast

The role of the unfolded protein response in myelination

@en

type

Item

label

The role of the unfolded protein response in myelination

@ast

The role of the unfolded protein response in myelination

@en

prefLabel

The role of the unfolded protein response in myelination

@ast

The role of the unfolded protein response in myelination

@en

P1476

The role of the unfolded protein response in myelination

@en

P2093

Jill M McMahon

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

Michelle C Naughton

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

Una F FitzGerald

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

P2860

Constitutive expression of heat shock proteins Hsp90, Hsc70, Hsp70 and Hsp60 in neural and non-neural tissues of the rat during postnatal development

Plasma cell differentiation initiates a limited ER stress response by specifically suppressing the PERK-dependent branch of the unfolded protein response.

Pharmaceutical integrated stress response enhancement protects oligodendrocytes and provides a potential multiple sclerosis therapeutic

The integrated stress response prevents demyelination by protecting oligodendrocytes against immune-mediated damage.

Oligodendrocyte-specific activation of PERK signaling protects mice against experimental autoimmune encephalomyelitis.

Calreticulin and other components of endoplasmic reticulum stress in rat and human inflammatory demyelination.

On the biogenesis of myelin membranes: sorting, trafficking and cell polarity.

Genetic inactivation of PERK signaling in mouse oligodendrocytes: normal developmental myelination with increased susceptibility to inflammatory demyelination.

Increased expression of ER stress- and hypoxia-associated molecules in grey matter lesions in multiple sclerosis.

P304

394-395

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

P31

scholarly article

P356

10.4103/1673-5374.179036

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

Una Fitzgerald

Jill McMahon

Michelle Naughton

P577

2016-03-01T00:00:00Z

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

P698

27127465

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

P932

4828991

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