Mitochondrial DNA (mtDNA) sequence variation and maternal inheritance are valuable tools in assessing ancestry of different human populations and for clinical practice. A new study (Wei et al., 2019) reports that the fate of new mtDNA variants in the female germline is non-random as they report functional selection and matching to nuclear ancestry to shape human mtDNA variation.Non peer reviewe
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
<div><p>Recent reports have questioned the accepted dogma that mammalian mitochondrial DNA (mtDNA) i...
There is an intense debate concerning whether selection or demographics has been most important in s...
Mitochondrial DNA (mtDNA) sequence variation and maternal inheritance are valuable tools in assessin...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
Background: Originally believed to be a rare phenomenon, heteroplasmy - the presence of more than on...
STUDY QUESTION Does mitochondrial DNA (mtDNA) diversity in modern human populations potentially pose...
Evidence for a biparental mode of mitochondrial DNA (mtDNA) inheritance has been sparse and remains ...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
Since the unexpected discovery that mitochondria contain their own distinct DNA molecules, studies o...
Abstract Most of the pathogenic variants in mitochondrial DNA (mtDNA) exist in a heteroplasmic state...
Heteroplasmy-the presence of multiple mitochondrial DNA (mtDNA) haplotypes in an individual-can lead...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
<div><p>Recent reports have questioned the accepted dogma that mammalian mitochondrial DNA (mtDNA) i...
There is an intense debate concerning whether selection or demographics has been most important in s...
Mitochondrial DNA (mtDNA) sequence variation and maternal inheritance are valuable tools in assessin...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
The manifestation of mitochondrial DNA (mtDNA) diseases depends on the frequency of heteroplasmy (th...
Background: Originally believed to be a rare phenomenon, heteroplasmy - the presence of more than on...
STUDY QUESTION Does mitochondrial DNA (mtDNA) diversity in modern human populations potentially pose...
Evidence for a biparental mode of mitochondrial DNA (mtDNA) inheritance has been sparse and remains ...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
Since the unexpected discovery that mitochondria contain their own distinct DNA molecules, studies o...
Abstract Most of the pathogenic variants in mitochondrial DNA (mtDNA) exist in a heteroplasmic state...
Heteroplasmy-the presence of multiple mitochondrial DNA (mtDNA) haplotypes in an individual-can lead...
With a combined carrier frequency of 1:200, heteroplasmic mitochondrial DNA (mtDNA) mutations cause ...
<div><p>Recent reports have questioned the accepted dogma that mammalian mitochondrial DNA (mtDNA) i...
There is an intense debate concerning whether selection or demographics has been most important in s...