Mitochondrial DNA: does more lead to less? (Q72640295)

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28 October 2019

title

Mitochondrial DNA: does more lead to less? (English)

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28 October 2019

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28 October 2019

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28 October 2019

publication date

1 December 1994

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28 October 2019

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28 October 2019

volume

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28 October 2019

issue

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28 October 2019

page(s)

313-315

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Sequence and organization of the human mitochondrial genome

28 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Duplications of mitochondrial DNA in mitochondrial myopathy

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Mitochondrial DNA and genetic disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Mitochondrial diabetes revisited

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

A new type of mitochondrial DNA deletion in patients with encephalomyopathy

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

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

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7 January 2021

A mitochondrial tRNA anticodon swap associated with a muscle disease

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Noninvasive diagnosis of the MELAS syndrome from blood DNA

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

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

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7 January 2021

Origin, transmission, and segregation of mitochondrial DNA dimers in mouse hybrid and cybrid cell lines

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7 January 2021

Circular Oligomers in Mitochondrial DNA of Human and Beef Nonmalignant Thyroid Glands

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7 January 2021

Multimerization of high copy number plasmids causes instability: Cole 1 encodes a determinant essential for plasmid monomerization and stability

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7 January 2021

The origins of replication of the yeast mitochondrial genome and the phenomenon of suppressivity

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Fetal growth and impaired glucose tolerance in men and women

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https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Hypertrophy and hyperplasia of the pancreatic islets in new-born infants

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Biochemical consequences of a large deletion in the mitochondrial genome of a Drosophila subobscura strain.

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Tandem duplications in animal mitochondrial DNAs: variation in incidence and gene content among lizards

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Evolution of plant mitochondrial genomes via substoichiometric intermediates

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Nuclear genotype affects mitochondrial genome organization of CMS-S maize

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-313

7 January 2021

Identifiers

DOI

10.1038/NG1294-313

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7894476%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7894476%20AND%20SRC:MED&resulttype=core&format=json