1. Associations of mitochondrial DNA 3777–4679 region mutations with maternally inherited essential hypertensive subjects in China
    Ye Zhu et al, 2020, BMC Medical Genetics CrossRef
  2. Novel mitochondrial tRNALeu(UUR) 3261A > g mutation in two pedigrees with essential hypertension
    Ye Fu et al, 2023, Irish Journal of Medical Science (1971 -) CrossRef
  3. Molecular characterization of two Chinese pedigrees with maternally inherited hypertension
    Yu Ding et al, 2021, The Journal of Gene Medicine CrossRef
  4. Comment on “Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis”
    Josef Finsterer et al, 2018, Oxidative Medicine and Cellular Longevity CrossRef
  5. Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber’s hereditary optic neuropathy
    Jie Shuai et al, 2022, Irish Journal of Medical Science (1971 -) CrossRef
  6. Mitochondrial tRNASer(UCN) 7471delC may be a novel mutation associated with maternally transmitted hypertension
    Ping Yang et al, 2020, Irish Journal of Medical Science (1971 -) CrossRef
  7. Mitochondrial tRNALeu(UUR) C3275T, tRNAGln T4363C and tRNALys A8343G mutations may be associated with PCOS and metabolic syndrome
    Yu Ding et al, 2018, Gene CrossRef
  8. Potential Roles of mtDNA Mutations in PCOS-IR: A Review
    Xiao-Chao Dong et al, 2023, Diabetes, Metabolic Syndrome and Obesity CrossRef
  9. The Role of Mitochondrial DNA Mutations in Cardiovascular Diseases
    Siarhei A. Dabravolski et al, 2022, International Journal of Molecular Sciences CrossRef