RML prions act through Mahogunin and Attractin-independent pathways. - Wikidata - wikimedia - TriplyDB

RML prions act through Mahogunin and Attractin-independent pathways.

RML prions act through Mahogunin and Attractin-independent pathways.

http://www.wikidata.org/entity/Q37523064

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A Homozygous RAB3GAP1:c.743delC Mutation in Rottweilers with Neuronal Vacuolation and Spinocerebellar Degeneration.Disturbed vesicular trafficking of membrane proteins in prion disease.

P2860

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P2860

RML prions act through Mahogunin and Attractin-independent pathways.

http://www.wikidata.org/entity/Q37523064

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 31 May 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

RML prions act through Mahogunin and Attractin-independent pathways.

@en

RML prions act through Mahogunin and Attractin-independent pathways.

@nl

type

label

RML prions act through Mahogunin and Attractin-independent pathways.

@en

RML prions act through Mahogunin and Attractin-independent pathways.

@nl

prefLabel

RML prions act through Mahogunin and Attractin-independent pathways.

@en

RML prions act through Mahogunin and Attractin-independent pathways.

@nl

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RML prions act through Mahogunin and Attractin-independent pathways.

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George A Carlson

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P2860

The mouse mahogany locus encodes a transmembrane form of human attractin

Spongiform neurodegeneration-associated E3 ligase Mahogunin ubiquitylates TSG101 and regulates endosomal trafficking

Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease

Loss of Vac14, a regulator of the signaling lipid phosphatidylinositol 3,5-bisphosphate, results in neurodegeneration in mice.

PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

Spongiform degeneration in mahoganoid mutant mice

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J

Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice

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267-271

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scholarly article

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10.4161/PRI.25054

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4

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240309119

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23787699

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Prion protein family

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3904309

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