(Q78109255)

English

Introduction of heteroplasmic mitochondrial DNA (mtDNA) from a patient with NARP into two human rho degrees cell lines is associated either with selection and maintenance of NARP mutant mtDNA or failure to maintain mtDNA

scientific article published on 01 September 1999

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scholarly article

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11 December 2019

Introduction of heteroplasmic mitochondrial DNA (mtDNA) from a patient with NARP into two human rho degrees cell lines is associated either with selection and maintenance of NARP mutant mtDNA or failure to maintain mtDNA (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10441339%20AND%20SRC:MED&resulttype=core&format=json

11 December 2019

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11 December 2019

author name string

L Vergani

1

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11 December 2019

R Rossi

2

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11 December 2019

C H Brierley

3

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11 December 2019

M Hanna

4

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11 December 2019

publication date

1 September 1999

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11 December 2019

Human Molecular Genetics

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11 December 2019

8

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11 December 2019

9

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11 December 2019

1751-1755

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11 December 2019

Molecular genetic aspects of human mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Behaviour of a population of partially duplicated mitochondrial DNA molecules in cell culture: segregation, maintenance and recombination dependent upon nuclear background

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

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

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

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

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

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

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Ethidium bromide-induced loss of mitochondrial DNA from primary chicken embryo fibroblasts

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybrids

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Mitochondrial DNA-like sequences in the human nuclear genome. Characterization and implications in the evolution of mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Co-amplification of nuclear pseudogenes and assessment of heteroplasmy of mitochondrial DNA mutations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Simplified mammalian DNA isolation procedure

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1751

21 January 2018

Identifiers

10.1093/HMG/8.9.1751

1 reference

Europe PubMed Central

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11 December 2019

1 reference

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11 December 2019

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