Wolfram syndrome: MAMs' connection? - Test2 - elhamkhani - TriplyDB

Wolfram syndrome: MAMs' connection?

Wolfram syndrome: MAMs' connection?

http://www.wikidata.org/entity/Q52671146

about

Mitochondria-associated membranes (MAMs) and pathologies.

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Q51733347-F805571F-0A85-427A-B1A2-430A0DCB2946

P2860

Wolfram syndrome: MAMs' connection?

http://www.wikidata.org/entity/Q52671146

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

Wolfram syndrome: MAMs' connection?

@en

Wolfram syndrome: MAMs' connection?

@nl

type

label

Wolfram syndrome: MAMs' connection?

@en

Wolfram syndrome: MAMs' connection?

@nl

prefLabel

Wolfram syndrome: MAMs' connection?

@en

Wolfram syndrome: MAMs' connection?

@nl

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S41419-018-0406-3

P1433

Cell Death and Disease

P1476

Wolfram syndrome: MAMs' connection?

@en

P2093

Benjamin Delprat

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

Tangui Maurice

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

P275

Creative Commons Attribution

P2860

Antagonism of Beclin 1-dependent autophagy by BCL-2 at the endoplasmic reticulum requires NAF-1

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

ER stress induces cleavage of membrane-bound ATF6 by the same proteases that process SREBPs

XBP1 mRNA is induced by ATF6 and spliced by IRE1 in response to ER stress to produce a highly active transcription factor

Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium

VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis

Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells

WFS1 protein modulates the free Ca(2+) concentration in the endoplasmic reticulum

Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

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364

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scholarly article

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10.1038/S41419-018-0406-3

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3

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9

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Cécile Delettre

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2018-03-06T00:00:00Z

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29511163

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Wolfram syndrome

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5840383

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