(Q28364171)

2

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M Warich-Kirches

3

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T Schneider

4

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S Weis

5

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G Krause

6

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C Mawrin

7

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K Dietzmann

Journal of Medical Genetics

8

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language of work or name

English

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publication date

May 2001

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published in

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volume

38

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issue

5

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page(s)

312-7

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cites work

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Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes

20 March 2017

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Drosophila Mitochondrial Genetics: Evolution of Heteroplasmy through Germ Line Cell Divisions

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The frequency of heteroplasmy in the HVII region of mtDNA differs across tissue types and increases with age.

29 September 2017

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Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variation

29 September 2017

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Evidence from human oocytes for a genetic bottleneck in an mtDNA disease

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Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck

29 September 2017

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A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle

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29 September 2017

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Rapid segregation of heteroplasmic bovine mitochondria

29 September 2017

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

29 September 2017

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Replacement of bovine mitochondrial DNA by a sequence variant within one generation

29 September 2017

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

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A specific point mutation in the mitochondrial genome of Caucasians with MELAS

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Loss of heteroplasmy in the displacement loop of brain mitochondrial DNA in astrocytic tumors.

2 June 2018

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Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

27 November 2018

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Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

27 November 2018

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Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging

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12 December 2020

Extremely high levels of human mitochondrial DNA heteroplasmy in single hair roots

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Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

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Mitochondrial DNA: does more lead to less?

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Mitochondrial Disorders

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12 December 2020