(Q40965450)

English

Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction

scientific article published on January 1999

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scholarly article

1 reference

Europe PubMed Central

25 September 2017

Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction (English)

1 reference

Europe PubMed Central

25 September 2017

mitochondrial DNA

0 references

author name string

Raha S

1

1 reference

Europe PubMed Central

25 September 2017

Merante F

2

1 reference

Europe PubMed Central

25 September 2017

Shoubridge E

3

1 reference

Europe PubMed Central

25 September 2017

Myint AT

4

1 reference

Europe PubMed Central

25 September 2017

Tein I

5

1 reference

Europe PubMed Central

25 September 2017

Benson L

6

1 reference

Europe PubMed Central

25 September 2017

Johns T

7

1 reference

Europe PubMed Central

25 September 2017

Robinson BH

8

1 reference

Europe PubMed Central

25 September 2017

publication date

1 January 1999

1 reference

Europe PubMed Central

25 September 2017

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Europe PubMed Central

25 September 2017

13

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Europe PubMed Central

25 September 2017

3

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Europe PubMed Central

25 September 2017

245-254

1 reference

Europe PubMed Central

25 September 2017

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

1 reference

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21 January 2018

Isolation and characterization of intraspecific cybrids. Effect of mitochondrial DNA on their cellular properties.

1 reference

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17 Predicting optimal and suboptimal secondary structure for RNA

1 reference

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21 January 2018

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

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21 January 2018

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

1 reference

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21 January 2018

Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations.

1 reference

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21 January 2018

Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome

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21 January 2018

Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy

1 reference

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21 January 2018

Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.

1 reference

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21 January 2018

Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

1 reference

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21 January 2018

Assignment of two mitochondrially synthesized polypeptides to human mitochondrial DNA and their use in the study of intracellular mitochondrial interaction

1 reference

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21 January 2018

Diagnosis of complex I deficiency in patients with lactic acidemia using skin fibroblast cultures.

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21 January 2018

Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia

1 reference

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21 January 2018

Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio

1 reference

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21 January 2018

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

1 reference

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21 January 2018

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

1 reference

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21 January 2018

Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function

1 reference

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21 January 2018

An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy

1 reference

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21 January 2018

Regulation of the expression of mitochondrial proteins: relationship between mtDNA copy number and cytochrome-c oxidase activity in human cells and tissues

1 reference

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21 January 2018

Identifiers

10.1002/(SICI)1098-1004(1999)13:3<245::AID-HUMU9>3.0.CO;2-B

1 reference

Europe PubMed Central

25 September 2017

release_hahtkyh6nrhtddd676sbya2uaq

1 reference

https://api.fatcat.wiki/v0/release/hahtkyh6nrhtddd676sbya2uaq

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

25 September 2017

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