Search
forResearch 10 of 1000+
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Alterations of plasma antioxidants and mitochondrial DNA mutation in hair follicles of smokers
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature
- Mitochondrial dysfunction as a cause of ageing
- <i>De novo</i> mutation in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- Stem cell identification-<i>in vivo</i> lineage analysis versus <i>in vitro</i> isolation and clonal expansion
- Fidelity of the Human Mitochondrial DNA Polymerase
- The legacy of Bruce Ames and mitochondrial DNA mutagenicity: integrating oxidative stress, aging, and modern perspectives
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →