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Journal Abstract Search

252 related items for PubMed ID: 32414374

  • 1. Associations of mitochondrial DNA 3777-4679 region mutations with maternally inherited essential hypertensive subjects in China.
    Zhu Y, You J, Xu C, Gu X.
    BMC Med Genet; 2020 May 15; 21(1):105. PubMed ID: 32414374
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  • 6. The Role of Mitochondrial DNA Mutations in Cardiovascular Diseases.
    Dabravolski SA, Khotina VA, Sukhorukov VN, Kalmykov VA, Mikhaleva LM, Orekhov AN.
    Int J Mol Sci; 2022 Jan 16; 23(2):. PubMed ID: 35055137
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  • 9. The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.
    Lu Z, Chen H, Meng Y, Wang Y, Xue L, Zhi S, Qiu Q, Yang L, Mo JQ, Guan MX.
    Eur J Hum Genet; 2011 Nov 16; 19(11):1181-6. PubMed ID: 21694735
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  • 13. [Mitochondrial DNA mutation associated with hypertension in tRNA(Ile) and tRNA(Gln) genes].
    Zhu C, Liu Y, Gao J, Yang J, Yin T, Lan Y, Li Z, Guan M, Li Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct 16; 31(5):619-22. PubMed ID: 25297595
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  • 16. A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.
    Tabebi M, Mkaouar-Rebai E, Mnif M, Kallabi F, Ben Mahmoud A, Ben Saad W, Charfi N, Keskes-Ammar L, Kamoun H, Abid M, Fakhfakh F.
    Biochem Biophys Res Commun; 2015 Apr 10; 459(3):353-60. PubMed ID: 25701779
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  • 17. Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
    Al-Kafaji G, Bakheit HF, AlAli F, Fattah M, Alhajeri S, Alharbi MA, Daif A, Alsabbagh MM, Alwehaidah MS, Bakhiet M.
    PLoS One; 2022 Apr 10; 17(2):e0263606. PubMed ID: 35130313
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  • 20. A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.
    Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM.
    J Am Coll Cardiol; 2003 May 21; 41(10):1786-96. PubMed ID: 12767666
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