The Salih ataxia mutation impairs Rubicon endosomal localization.

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The clearance of dying cells: table for two New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations Systematic review of autosomal recessive ataxias and proposal for a classification.Rubicon: LC3-associated phagocytosis and beyond.

P2860

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P2860

The Salih ataxia mutation impairs Rubicon endosomal localization.

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http://www.wikidata.org/entity/Q50943825

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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name

The Salih ataxia mutation impairs Rubicon endosomal localization.

@en

The Salih ataxia mutation impairs Rubicon endosomal localization.

@nl

type

Item

label

The Salih ataxia mutation impairs Rubicon endosomal localization.

@en

The Salih ataxia mutation impairs Rubicon endosomal localization.

@nl

prefLabel

The Salih ataxia mutation impairs Rubicon endosomal localization.

@en

The Salih ataxia mutation impairs Rubicon endosomal localization.

@nl

P1476

The Salih ataxia mutation impairs Rubicon endosomal localization

@en

P2093

A Martelli

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

M Assoum

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

M Koenig

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

N Drouot

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

P2860

Functional characterization of Rab7 mutant proteins associated with Charcot-Marie-Tooth type 2B disease

Two Beclin 1-binding proteins, Atg14L and Rubicon, reciprocally regulate autophagy at different stages

Distinct regulation of autophagic activity by Atg14L and Rubicon associated with Beclin 1-phosphatidylinositol-3-kinase complex

Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy.

The autosomal recessive cerebellar ataxias.

Rubicon controls endosome maturation as a Rab7 effector

Rubicon and PLEKHM1 negatively regulate the endocytic/autophagic pathway via a novel Rab7-binding domain.

Interaction between small GTPase Rab7 and PI3KC3 links autophagy and endocytosis: A new Rab7 effector protein sheds light on membrane trafficking pathways.

Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxia.

P2888

s12311-013-0489-4

P304

835-840

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P31

scholarly article

P356

10.1007/S12311-013-0489-4

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P433

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

P478

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

P50

Mustafa A. Salih

Karim Hnia

P577

2013-12-01T00:00:00Z

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P5875

237004984

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P698

23728897

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The Salih ataxia mutation impairs Rubicon endosomal localization.

about

P2860

P2860

The Salih ataxia mutation impairs Rubicon endosomal localization.

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