(Q34747246)

4 August 2017

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

1 reference

4 August 2017

M F Alexeyev

1

1 reference

4 August 2017

N Venediktova

2

1 reference

4 August 2017

V Pastukh

3

1 reference

4 August 2017

I Shokolenko

4

1 reference

4 August 2017

G Bonilla

5

1 reference

4 August 2017

G L Wilson

6

1 reference

4 August 2017

7 February 2008

1 reference

4 August 2017

1 reference

4 August 2017

15

1 reference

4 August 2017

516-523

1 reference

4 August 2017

7

1 reference

https://scigraph.springernature.com/pub.10.1038/gt.2008.11

4 August 2017

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

Mitochondrial DNA mutations in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Mitochondrial disease

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Mitochondrial threshold effects.

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Mitochondrial DNA and disease

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

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.

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Lactic acidemia and mitochondrial disease

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Developing a systematic approach to the diagnosis and classification of mitochondrial disease

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Manipulating mitochondrial DNA heteroplasmy by a mitochondrially targeted restriction endonuclease

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Measurements of ATP in mammalian cells

1 reference

https://api.crossref.org/works/10.1038%2FGT.2008.11

7 January 2021

Identifiers

DOI

10.1038/GT.2008.11

1 reference

release_3ykbiqla6zhr5fuht56fevd5hu

4 August 2017

1 reference

Fatcat

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

24 November 2022

mapped directly with Wikidata item

1 reference