Examples of 'mtdna' in a sentence
Meaning of "mtdna"
MtDNA is a noun that stands for 'mitochondrial DNA,' genetic material found in mitochondria
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- Abbreviation of mitochondrial DNA.
- Alternative form of mtDNA
How to use "mtdna" in a sentence
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mtdna
This is supported by mtDNA cytochrome b sequence analysis.
Complimentary evidence exists from mtDNA data.
Increased mtDNA damage is a feature of several neurodegenerative diseases.
This results in two new mtDNA molecules.
The mtDNA are extra copies of genes.
These genes are critical for mtDNA maintenance.
The mtDNA comes only from our mothers.
The same concept exists for mtDNA.
Mutations in mtDNA cause human diseases.
These results were supported by mtDNA analyses.
Three regions of mtDNA also provide diagnostic species markers.
The second adds the various mtDNA haplogroups.
For mtDNA there can be dozens to hundreds in each cell.
Only one of them has contributed your mtDNA.
A disadvantage of mtDNA is that only the maternal line is represented.
See also
We can see this in their mtDNA.
Human mtDNA can also be used to help identify individuals.
Therefore all children of a female are clonal for mtDNA.
Scroll down until you see mtDNA haplogroups.
This method can be used to manipulate or replace mtDNA.
These characteristics make targeting mtDNA a practical therapeutic strategy.
The mtDNA variation was distributed unevenly in the populations studied.
It might be argued that some mtDNA lines are later divisions.
Many cancer types are the result of mutations in the mtDNA.
We show the absence of gray wolf mtDNA in these wolves.
In one embodiment this method is used to manipulate or replace mtDNA.
Deletions or mutations to segments of mtDNA lead to defective function of oxidative phosphorylation.
It was destroyed to investigate the mtDNA.
Some authors cite paternal mtDNA transmission as invalidating mtDNA testing.
Mitochondrial disease is the result of spontaneous mutations in mtDNA or nDNA.
An mtDNA test will identify how closely related you are to a haplogroup.
Each of these mitochondria contain at least one copy of mtDNA.
Analysis of mtDNA in these same embryos showed exclusively maternal mtDNA.
Any form of mutation in twinkle protein can result in to mtDNA disease.
A unique mtDNA sequence.
Stock discriminatory power was tested by computing allocation efficiencies of mtDNA characters.
The percentage of mutated mtDNA is presumed to increase with age in muscle.
Diseases linked to mtDNA.
A higher percentage of mutated mtDNA typically leads to more severe disease.
There were no known mistakes made in the microscopic hair or mtDNA analyses.
A higher percentage of mutated mtDNA typically causes more severe disease.
An mtDNA is genetic material contained in the cellular organelle called the mitochondria.
The method is preferably used to examine mtDNA from a human subject.
The mtDNA research confirms most of the other new findings in archaeology.
Recent studies indicate that mutations in mtdna are selectively eliminated in the germline.
Its entire mtDNA control region haplotype was obtained by two independent laboratories.
Looking at it from the point of view of mtDNA was not entirely satisfactory either.
A single mtDNA sequence variant usually exists in all cells of most humans.
There is debate over whether or not paternal mtDNA transmission is possible in humans.
The number of mtDNA copies in human cells differs widely by cell type.
