(Q33737272)

29 July 2017

1 reference

title

Mitochondria harbouring mutant mtDNA--a cuckoo in the nest? (English)

1 reference

29 July 2017

1 reference

Hofhaus G

1

1 reference

PubMed ID

10494836

29 July 2017

Gattermann N

series ordinal

2

1 reference

29 July 2017

1 July 1999

1 reference

29 July 2017

1 reference

29 July 2017

380

1 reference

29 July 2017

871-877

1 reference

29 July 2017

7-8

1 reference

MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase.

29 July 2017

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Highly efficient DNA synthesis in isolated mitochondria from rat liver.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

The synthesis of mRNA in isolated mitochondria can be maintained for several hours and is inhibited by high levels of ATP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Human mitochondria and mitochondrial genome function as a single dynamic cellular unit

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Somatic mutations of the mitochondrial genome in human colorectal tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Mitochondrial complex I deficiency in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Mitochondrial DNA maintenance in vertebrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Preferential amplification and phenotypic selection in a population of deleted and wild-type mitochondrial DNA in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Origin and functional consequences of the complex I defect in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

Mitochondrial diseases in man and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.107

21 January 2018

Identifiers

DOI

10.1515/BC.1999.107

1 reference

29 July 2017

1 reference

PubMed ID

10494836