(Q34747246)

4 August 2017

title

Selective elimination of mutant mitochondrial genomes as therapeutic strategy for the treatment of NARP and MILS syndromes (English)

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4 August 2017

M F Alexeyev

1

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4 August 2017

N Venediktova

2

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4 August 2017

V Pastukh

3

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4 August 2017

I Shokolenko

4

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4 August 2017

G Bonilla

5

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4 August 2017

G L Wilson

6

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4 August 2017

publication date

7 February 2008

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4 August 2017

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4 August 2017

volume

15

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4 August 2017

issue

7

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4 August 2017

page(s)

516-523

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The encephalomyocarditis virus internal ribosome entry site allows efficient coexpression of two genes from a recombinant provirus in cultured cells and in embryos

4 August 2017

cites work

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Mitochondrial disease

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A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

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Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993

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7 January 2021

The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?

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Mitochondrial DNA and disease

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7 January 2021

Correlation between the Clinical Symptoms and the Proportion of Mitochondrial DNA Carrying the 8993 Point Mutation in the NARP Syndrome

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7 January 2021

Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit a

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7 January 2021

Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA.

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7 January 2021

An adenovirus type 5 (Ad5) amplicon-based packaging cell line for production of high-capacity helper-independent deltaE1-E2-E3-E4 Ad5 vectors

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Skipping the co-expression problem: the new 2A "CHYSEL" technology

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Mutations in the passenger polypeptide can affect its partitioning between mitochondria and cytoplasm: mutations can impair the mitochondrial import of DsRed

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Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts

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Lactic acidemia and mitochondrial disease

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7 January 2021

Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus

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7 January 2021

Gene therapy of mitochondrial DNA mutations: a brief, biased history of allotopic expression in mammalian cells

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7 January 2021

Limitations to in vivo import of hydrophobic proteins into yeast mitochondria. The case of a cytoplasmically synthesized apocytochrome b

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7 January 2021

Manipulating mitochondrial DNA heteroplasmy by a mitochondrially targeted restriction endonuclease

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7 January 2021

Rapid directional shift of mitochondrial DNA heteroplasmy in animal tissues by a mitochondrially targeted restriction endonuclease

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7 January 2021

Sequence-specific modification of mitochondrial DNA using a chimeric zinc finger methylase

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7 January 2021

Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene.

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7 January 2021

Gene synthesis, bacterial expression and purification of the Rickettsia prowazekii ATP/ADP translocase

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7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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7 January 2021

Measurements of ATP in mammalian cells

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7 January 2021

Identifiers

DOI

10.1038/GT.2008.11

1 reference

release_3ykbiqla6zhr5fuht56fevd5hu

4 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3ykbiqla6zhr5fuht56fevd5hu

24 November 2022

mapped directly with Wikidata item

1 reference