Wang L, Dong Z, Lin W, Gao R, Chen C, Xu J. Molecular characterization of a pedigree carrying the hypertensionassociated mitochondrial tRNAGln T4363C mutation. Mol Med Rep. 2017;16(5):6029–33.
Article
CAS
PubMed
PubMed Central
Google Scholar
Shen Y, Peng X, Wang M, Zheng X, Xu G, Lu L, Xu K, Burstrom B, Burstrom K, Wang J. Family member-based supervision of patients with hypertension: a cluster randomized trial in rural China. J Hum Hypertens. 2017;31(1):29–36.
Article
CAS
PubMed
Google Scholar
Qiu Q, Li R, Jiang P, Xue L, Lu Y, Song Y, Han J, Lu Z, Zhi S, Mo JQ, et al. Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees. Hum Mutat. 2012;33(8):1285–93.
Article
CAS
PubMed
Google Scholar
Schapira AH. Mitochondrial disease. Lancet (London, England). 2006;368(9529):70–82.
Article
CAS
Google Scholar
Inaba Y, Chen JA, Bergmann SR. Carotid plaque, compared with carotid intima-media thickness, more accurately predicts coronary artery disease events: a meta-analysis. Atherosclerosis. 2012;220(1):128–33.
Article
CAS
PubMed
Google Scholar
Liu P, Demple B. DNA repair in mammalian mitochondria: much more than we thought? Environ Mol Mutagen. 2010;51(5):417–26.
CAS
PubMed
Google Scholar
Lu Z, Chen H, Meng Y, Wang Y, Xue L, Zhi S, Qiu Q, Yang L, Mo JQ, Guan MX. The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree. Eur J Human Genet. 2011;19(11):1181–6.
Article
CAS
Google Scholar
Chen H, Sun M, Fan Z, Tong M, Chen G, Li D, Ye J, Yang Y, Zhu Y, Zhu J. Mitochondrial C4375T mutation might be a molecular risk factor in a maternal Chinese hypertensive family under haplotype C. Clin Exp Hypertens. 2018;40(6):518–23.
Article
CAS
PubMed
Google Scholar
Kirichenko TV, Sobenin IA, Khasanova ZB, Orekhova VA, Melnichenko AA, Demakova NA, Grechko AV, Orekhov AN, Ble Castillo JL, Shkurat TP. Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: comparison of samples from Russian and Mexican populations. Data Brief. 2018;18:16–21.
Article
PubMed
PubMed Central
Google Scholar
Deng H, Yuan L. Molecular genetics of congenital nuclear cataract. Eur J Med Genet. 2014;57(2–3):113–22.
Article
PubMed
Google Scholar
Zhu HY, Wang SW, Martin LJ, Liu L, Li YH, Chen R, Wang L, Zhang ML, Benson DW. The role of mitochondrial genome in essential hypertension in a Chinese Han population. Eur J Human Genet. 2009;17(11):1501–6.
Article
CAS
Google Scholar
Han GX, Song Y, Chen L, Zhai YZ, Dong J, Li TS, Zhu HY. The role of mitochondrial DNA mutations in a Han Chinese population on sepsis pathogenesis. Eur Rev Med Pharmacol Sci. 2017;21(14):3247–52.
PubMed
Google Scholar
Chalmers J, MacMahon S, Mancia G, Whitworth J, Beilin L, Hansson L, Neal B, Rodgers A, Ni Mhurchu C, Clark T. World Health Organization-International Society of Hypertension Guidelines for the management of hypertension. Guidelines sub-committee of the World Health Organization. Clin Exp Hypertension (New York, NY : 1993). 1999;21(5–6):1009–60.
CAS
Google Scholar
Liu LS. Chinese guidelines for the management of hypertension. Zhonghua xin xue guan bing za zhi 2011. 2010;39(7):579–615.
Google Scholar
Zhu HY, Wang SW, Liu L, Li YH, Chen R, Wang L, Holliman CJ. A mitochondrial mutation A4401G is involved in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives. Eur J Human Genet. 2009;17(2):172–8.
Article
CAS
Google Scholar
Liu Y, Li Y, Gao J, Zhu C, Lan Y, Yang J, Li Z, Guan M, Chen Y. Molecular characterization of a Chinese family carrying a novel C4329A mutation in mitochondrial tRNAIle and tRNAGln genes. BMC Med Genet. 2014;15:84.
Article
PubMed
PubMed Central
Google Scholar
Echem C, Costa TJD, Oliveira V, Giglio Colli L, Landgraf MA, Rodrigues SF, Franco M, Landgraf RG, Santos-Eichler RA, Bomfim GF, et al. Mitochondrial DNA: a new driver for sex differences in spontaneous hypertension. Pharmacol Res. 2019;144:142–50.
Article
CAS
PubMed
Google Scholar
Zhu Y, Gu X, Xu C. Mitochondrial DNA 7908-8816 region mutations in maternally inherited essential hypertensive subjects in China. BMC Med Genet. 2018;11(1):89.
CAS
Google Scholar
Ingman M, Gyllensten U. mtDB: human mitochondrial genome database, a resource for population genetics and medical sciences. Nucleic Acids Res. 2006;34(Database issue):D749–51.
Article
CAS
PubMed
Google Scholar
Samuels DC, Li C, Li B, Song Z, Torstenson E, Boyd Clay H, Rokas A, Thornton-Wells TA, Moore JH, Hughes TM, et al. Recurrent tissue-specific mtDNA mutations are common in humans. PLoS Genet. 2013;9(11):e1003929.
Article
PubMed
PubMed Central
Google Scholar
Bruno RM, Pucci G, Rosticci M, Guarino L, Guglielmo C, Agabiti Rosei C, Monticone S, Giavarini A, Lonati C, Torlasco C, et al. Association between lifestyle and systemic arterial hypertension in young adults: a national, survey-based, cross-sectional study. High Blood Press Cardiovasc Prev. 2016;23(1):31–40.
Article
CAS
PubMed
Google Scholar
Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL Jr, Jones DW, Materson BJ, Oparil S, Wright JT Jr, et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension (Dallas, Tex : 1979). 2003;42(6):1206–52.
Article
CAS
Google Scholar
Chen X, Zhang Y, Xu B, Cai Z, Wang L, Tian J, Liu Y, Li Y. The mitochondrial calcium uniporter is involved in mitochondrial calcium cycle dysfunction: underlying mechanism of hypertension associated with mitochondrial tRNA (Ile) A4263G mutation. Int J Biochem Cell Biol. 2016;78:307–14.
Article
CAS
PubMed
Google Scholar
Zhou M, Wang M, Xue L, Lin Z, He Q, Shi W, Chen Y, Jin X, Li H, Jiang P, et al. A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNA (Leu (UUR)). J Biol Chem. 2017;292(34):13934–46.
Article
CAS
PubMed
PubMed Central
Google Scholar
Zhao Y, Chen X, Li H, Zhu C, Li Y, Liu Y. Mitochondrial genome mutations in 13 subunits of respiratory chain complexes in Chinese Han and Mongolian hypertensive individuals. Mitochondrial DNA A DNA Mapp Seq Anal. 2018;29(7):1090–9.
CAS
PubMed
Google Scholar
Shimizu A, Mito T, Hayashi C, Ogasawara E, Koba R, Negishi I, Takenaga K, Nakada K, Hayashi J. Transmitochondrial mice as models for primary prevention of diseases caused by mutation in the tRNA (Lys) gene. Proc Natl Acad Sci U S A. 2014;111(8):3104–9.
Article
CAS
PubMed
PubMed Central
Google Scholar
Mohanty K, Dada R, Dada T. Neurodegenerative Eye Disorders: Role of Mitochondrial Dynamics and Genomics. Asia-Pac J Ophthalmology (Philadelphia, Pa). 2016;5(4):293–9.
Article
CAS
Google Scholar
Zhou H, Nie K, Qiu R, Xiong J, Shao X, Wang B, Shen L, Lyu J, Fang H. Generation and bioenergetic profiles of Cybrids with east Asian mtDNA Haplogroups. Oxidative Med Cell Longev. 2017;2017:1062314.
Google Scholar
Crescenzo R, Bianco F, Falcone I, Coppola P, Liverini G, Iossa S. Increased hepatic de novo lipogenesis and mitochondrial efficiency in a model of obesity induced by diets rich in fructose. Eur J Nutr. 2013;52(2):537–45.
Article
CAS
PubMed
Google Scholar
Singh A, Pezeshki A, Zapata RC, Yee NJ, Knight CG, Tuor UI, Chelikani PK. Diets enriched in whey or casein improve energy balance and prevent morbidity and renal damage in salt-loaded and high-fat-fed spontaneously hypertensive stroke-prone rats. J Nutr Biochem. 2016;37:47–59.
Article
CAS
PubMed
Google Scholar
Rocha MC, Rosa HS, Grady JP, Blakely EL, He L, Romain N, Haller RG, Newman J, McFarland R, Ng YS, et al. Pathological mechanisms underlying single large-scale mitochondrial DNA deletions. Ann Neurol. 2018;83(1):115–30.
Article
CAS
PubMed
PubMed Central
Google Scholar
Lehmann D, Tuppen HAL, Campbell GE, Alston CL, Lawless C, Rosa HS, Rocha MC, Reeve AK, Nicholls TJ, Deschauer M, et al. Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level. Nucleic Acids Res. 2019.
Moskalev AA, Aliper AM, Smit-McBride Z, Buzdin A, Zhavoronkov A. Genetics and epigenetics of aging and longevity. Cell cycle (Georgetown, Tex). 2014;13(7):1063–77.
Article
CAS
Google Scholar
Herbers E, Kekalainen NJ, Hangas A, Pohjoismaki JL, Goffart S. Tissue specific differences in mitochondrial DNA maintenance and expression. Mitochondrion. 2019;44:85–92.
Article
CAS
PubMed
Google Scholar