Associated Papers
Investigation of cytochrome B mutations, and UCP2 and STC1 gene expressions in patients with bipolar disorder.
Karabulut Uzunçakmak S et al.
Psychiatric Genetics, 2025
Mitochondrial DNA haplogroups J and T increase the risk of glioma.
González MDM et al.
Mitochondrion, 2021
Mitochondrial DNA abnormalities provide mechanistic insight and predict reactive oxygen species-stimulating drug efficacy.
Zaidieh T et al.
Bmc Cancer, 2021
Severe septic patients with mitochondrial DNA haplogroup JT show higher survival rates: a prospective, multicenter, observational study.
Lorente L et al.
Plos One, 2013
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
Ji Y et al.
American Journal of Human Genetics, 2008
Mitochondrial DNA haplogroups: role in the prevalence and severity of knee osteoarthritis.
Rego-Pérez I et al.
Arthritis and Rheumatism, 2008
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
Hudson G et al.
American Journal of Human Genetics, 2007
CD4+ T-cell response to mitochondrial cytochrome B in human melanoma.
Voo KS et al.
Cancer Research, 2006
Natural selection shaped regional mtDNA variation in humans.
Mishmar D et al.
Proceedings of the National Academy of Sciences of the United States of America, 2003
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