Gene therapy for the treatment of mitochondrial DNA disorders. - Wikidata - awgldk - TriplyDB

Gene therapy for the treatment of mitochondrial DNA disorders.

Gene therapy for the treatment of mitochondrial DNA disorders.

http://www.wikidata.org/entity/Q34401459

about

mtDNA T8993G mutation-induced mitochondrial complex V inhibition augments cardiolipin-dependent alterations in mitochondrial dynamics during oxidative, Ca(2+), and lipid insults in NARP cybrids: a potential therapeutic target for melatonin.

P2860

Q39495829-EBC598BE-E7BA-4655-AB43-CA2EE0D9519E

P2860

Gene therapy for the treatment of mitochondrial DNA disorders.

http://www.wikidata.org/entity/Q34401459

description

2005 nî lūn-bûn

@nan

2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

Gene therapy for the treatment of mitochondrial DNA disorders.

@ast

Gene therapy for the treatment of mitochondrial DNA disorders.

@en

Gene therapy for the treatment of mitochondrial DNA disorders.

@nl

type

label

Gene therapy for the treatment of mitochondrial DNA disorders.

@ast

Gene therapy for the treatment of mitochondrial DNA disorders.

@en

Gene therapy for the treatment of mitochondrial DNA disorders.

@nl

prefLabel

Gene therapy for the treatment of mitochondrial DNA disorders.

@ast

Gene therapy for the treatment of mitochondrial DNA disorders.

@en

Gene therapy for the treatment of mitochondrial DNA disorders.

@nl

P1433

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P1476

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P2093

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P2860

Q34401459-036CF2D5-37B6-4338-8430-8AA4ADA7E835

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P356

14712598.5.2.183

P1433

Expert Opinion on Biological Therapy

P1476

Gene therapy for the treatment of mitochondrial DNA disorders.

@en

P2093

Robert W Taylor

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

P2860

Premature ageing in mice expressing defective mitochondrial DNA polymerase

Paternal inheritance of mitochondrial DNA

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants

Complete restoration of a wild-type mtDNA genotype in regenerating muscle fibres in a patient with a tRNA point mutation and mitochondrial encephalomyopathy

Mitochondrial disorders

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

Mitochondrial myopathy caused by long-term zidovudine therapy

Mitochondrial respiratory-chain diseases

Assembly of functional proton-translocating ATPase complex in yeast mitochondria with cytoplasmically synthesized subunit 8, a polypeptide normally encoded within the organelle.

P304

183-194

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

P31

scholarly article

P356

10.1517/14712598.5.2.183

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

P407

P433

2

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

P478

5

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

P577

2005-02-01T00:00:00Z

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

P698

15757380

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

P921

mitochondrial DNA