Mitochondrial Dysfunction in Lysosomal Storage Disorders.

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Metabolic reprogramming in the pathogenesis of chronic lung diseases including BPD, COPD, and pulmonary fibrosis.Aminochrome Induces Irreversible Mitochondrial Dysfunction by Inducing Autophagy Dysfunction in Parkinson's Disease.

P2860

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Mitochondrial Dysfunction in Lysosomal Storage Disorders.

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http://www.wikidata.org/entity/Q41970073

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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

Mitochondrial Dysfunction in Lysosomal Storage Disorders.

@en

type

Item

label

Mitochondrial Dysfunction in Lysosomal Storage Disorders.

@en

prefLabel

Mitochondrial Dysfunction in Lysosomal Storage Disorders.

@en

P1476

Mitochondrial Dysfunction in Lysosomal Storage Disorders.

@en

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David Cotán

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

Gustavo Tiscornia

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

Isabel de Lavera

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

Manuel Oropesa-Ávila

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

Marina Villanueva-Paz

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

Mónica Álvarez-Córdoba

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P2860

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis

The cell biology of disease: lysosomal storage disorders: the cellular impact of lysosomal dysfunction

Selective degradation of mitochondria by mitophagy

Autophagy and mitochondria in Pompe disease: nothing is so new as what has long been forgotten

Glucocerebrosidase 1 deficient Danio rerio mirror key pathological aspects of human Gaucher disease and provide evidence of early microglial activation preceding alpha-synuclein-independent neuronal cell death

Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model.

Viable neuronopathic Gaucher disease model in Medaka (Oryzias latipes) displays axonal accumulation of alpha-synuclein

Mitochondrial dysfunction associated with glucocerebrosidase deficiency

A block of autophagy in lysosomal storage disorders

MLN64 mediates egress of cholesterol from endosomes to mitochondria in the absence of functional Niemann-Pick Type C1 protein

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scholarly article

P356

10.3390/DISEASES4040031

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P433

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

P478

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

P50

Juan Miguel Suárez-Rivero

Raquel Luzón-Hidalgo

Mario De la Mata

P577

2016-10-11T00:00:00Z

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P698

28933411

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P932

5456326

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Mitochondrial Dysfunction in Lysosomal Storage Disorders.

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P2860

P2860

Mitochondrial Dysfunction in Lysosomal Storage Disorders.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P50

P577

P698

P932