(Q34085604)

30 July 2017

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title

Mitochondrial genetics and disease. (English)

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30 July 2017

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Schon EA

1

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30 July 2017

1 November 2000

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30 July 2017

6

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Trends in Biochemical Sciences

inferred from page(s)

published in

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30 July 2017

25

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30 July 2017

555-560

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30 July 2017

11

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Sequence and organization of the human mitochondrial genome

30 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

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/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Mutations in mtDNA: are we scraping the bottom of the barrel?

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Mitochondrial respiratory chain diseases and mutations in nuclear DNA: a promising start?

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Mitochondrial DNA mutations and pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Mitochondrial deafness mutations reviewed

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Clinical, biochemical and molecular genetic features of Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Facile detection of mitochondrial DNA mutations in tumors and bodily fluids

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Cytochrome c oxidase: structure and spectroscopy.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Mitochondrial copper metabolism in yeast: mutational analysis of Sco1p involved in the biogenesis of cytochrome c oxidase

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Molecular architecture of the rotary motor in ATP synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

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/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Structural changes linked to proton translocation by subunit c of the ATP synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation. Comparison with the enzyme in Rho(0) cells completely lacking mtdna

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Neurotrophin-4 is up-regulated in ragged-red fibers associated with pathogenic mitochondrial DNA mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Tissue variation in the control of oxidative phosphorylation: implication for mitochondrial diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Mitochondria and skin disease

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Hepatotoxicity due to mitochondrial dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Kearns-sayre syndrome: oncocytic transformation of choroid plexus epithelium

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

The machinery of mitochondrial inheritance and behavior

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar system.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Localized firefly luciferase probes ATP at the surface of mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

Glucose generates sub-plasma membrane ATP microdomains in single islet beta-cells. Potential role for strategically located mitochondria.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901688-1

7 January 2021

10.1016/S0968-0004(00)01688-1

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

11084368