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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

231 related items for PubMed ID: 19546379

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  • 8. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
    Tang X, Li R, Zheng J, Cai Q, Zhang T, Gong S, Zheng W, He X, Zhu Y, Xue L, Yang A, Yang L, Lu J, Guan MX.
    Mol Genet Metab; 2010 May; 100(1):57-64. PubMed ID: 20153673
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  • 11. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
    Qu J, Li R, Zhou X, Tong Y, Lu F, Qian Y, Hu Y, Mo JQ, West CE, Guan MX.
    Invest Ophthalmol Vis Sci; 2006 Feb; 47(2):475-83. PubMed ID: 16431939
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  • 12. Coronary heart disease is associated with a mutation in mitochondrial tRNA.
    Jia Z, Wang X, Qin Y, Xue L, Jiang P, Meng Y, Shi S, Wang Y, Qin Mo J, Guan MX.
    Hum Mol Genet; 2013 Oct 15; 22(20):4064-73. PubMed ID: 23736300
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  • 13. A mitochondrial mutation A4401G is involved in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives.
    Zhu HY, Wang SW, Liu L, Li YH, Chen R, Wang L, Holliman CJ.
    Eur J Hum Genet; 2009 Feb 15; 17(2):172-8. PubMed ID: 18701880
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  • 16. Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.
    Liu XL, Zhou X, Zhou J, Zhao F, Zhang J, Li C, Ji Y, Zhang Y, Wei QP, Sun YH, Yang L, Lin B, Yuan Y, Li Y, Qu J, Guan MX.
    Ophthalmology; 2011 May 15; 118(5):978-85. PubMed ID: 21131053
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  • 18. Mitochondrial tRNALeu(UUR) C3275T, tRNAGln T4363C and tRNALys A8343G mutations may be associated with PCOS and metabolic syndrome.
    Ding Y, Xia BH, Zhang CJ, Zhuo GC.
    Gene; 2018 Feb 05; 642():299-306. PubMed ID: 29155328
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  • 19. The mitochondrial ND1 T3308C mutation in a Chinese family with the secondary hypertension.
    Liu Y, Li Z, Yang L, Wang S, Guan MX.
    Biochem Biophys Res Commun; 2008 Mar 28; 368(1):18-22. PubMed ID: 18194667
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