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Journal Abstract Search

242 related items for PubMed ID: 30336267

  • 41. Is mitochondrial tRNA(Ser(UCN)) T7501C mutation associated with cardiovascular disease?
    Ding Y, Huang J.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016; 27(1):205-8. PubMed ID: 24491108
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  • 42. [Pedigree analysis and sequence analysis of mtDNA 12srRNA, tRNA(Leu(UUR)), tRNA(Ser(UCN)) gene in nonsyndromic inherited deafness pedigrees].
    Li W, Han D, Yuan H, Cao J.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2004 Oct; 18(10):582-5, 589. PubMed ID: 15620132
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  • 43. Low penetrance of hearing loss in two Chinese families carrying the mitochondrial tRNASer(UCN) mutations.
    Peng W, Zhong Y, Zhao X, Yuan J.
    Mol Med Rep; 2020 Jul; 22(1):77-86. PubMed ID: 32377700
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  • 45. Late onset of type 2 diabetes is associated with mitochondrial tRNATrp A5514G and tRNASer(AGY) C12237T mutations.
    Yang L, Guo Q, Leng J, Wang K, Ding Y.
    J Clin Lab Anal; 2022 Jan; 36(1):e24102. PubMed ID: 34811812
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  • 48. Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.
    Gutiérrez Cortés N, Pertuiset C, Dumon E, Börlin M, Hebert-Chatelain E, Pierron D, Feldmann D, Jonard L, Marlin S, Letellier T, Rocher C.
    Hum Mutat; 2012 Apr; 33(4):681-9. PubMed ID: 22241583
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  • 50. Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.
    Bornstein B, Mas JA, Patrono C, Fernández-Moreno MA, González-Vioque E, Campos Y, Carrozzo R, Martín MA, del Hoyo P, Santorelli FM, Arenas J, Garesse R.
    Biochem J; 2005 May 01; 387(Pt 3):773-8. PubMed ID: 15554876
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  • 52. Molecular pathogenetic mechanism of maternally inherited deafness.
    Guan MX.
    Ann N Y Acad Sci; 2004 Apr 01; 1011():259-71. PubMed ID: 15126302
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  • 54. A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss.
    Cardaioli E, Da Pozzo P, Gallus GN, Malandrini A, Gambelli S, Gaudiano C, Malfatti E, Viscomi C, Zicari E, Berti G, Serni G, Dotti MT, Federico A.
    Neuromuscul Disord; 2007 Oct 01; 17(9-10):681-3. PubMed ID: 17614276
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  • 56. Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.
    Subathra M, Ramesh A, Selvakumari M, Karthikeyen NP, Srisailapathy CR.
    Ann Hum Genet; 2016 Sep 01; 80(5):257-73. PubMed ID: 27530448
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  • 59. Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation.
    Maász A, Komlósi K, Hadzsiev K, Szabó Z, Willems PJ, Gerlinger I, Kosztolányi G, Méhes K, Melegh B.
    Curr Med Chem; 2008 Sep 01; 15(13):1257-62. PubMed ID: 18537605
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  • 60. Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene.
    Bidooki S, Jackson MJ, Johnson MA, Chrzanowska-Lightowlers ZM, Taylor RW, Venables G, Lightowlers RN, Turnbull DM, Bindoff LA.
    Neuromuscul Disord; 2004 Jul 01; 14(7):417-20. PubMed ID: 15210164
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