These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 35685248)

  • 21. Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases.
    Mkaouar-Rebai E; Tlili A; Masmoudi S; Belguith N; Charfeddine I; Mnif M; Triki C; Fakhfakh F
    Biochem Biophys Res Commun; 2007 Apr; 355(4):1031-7. PubMed ID: 17336924
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.
    Hotta O; Inoue CN; Miyabayashi S; Furuta T; Takeuchi A; Taguma Y
    Kidney Int; 2001 Apr; 59(4):1236-43. PubMed ID: 11260383
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel mitochondrial tRNA
    Fu Y; Jing P; Yao L; Wang H; Zhou C
    Ir J Med Sci; 2023 Apr; 192(2):615-623. PubMed ID: 35657541
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Contribution of the tRNA
    Meng F; He Z; Tang X; Zheng J; Jin X; Zhu Y; Ren X; Zhou M; Wang M; Gong S; Mo JQ; Shu Q; Guan MX
    J Biol Chem; 2018 Mar; 293(9):3321-3334. PubMed ID: 29348176
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Search for mitochondrial A3243G tRNA(Leu) mutation in Polish patients with type 2 diabetes mellitus.
    Małecki M; Klupa T; Wanic K; Frey J; Cyganek K; Sieradzki J
    Med Sci Monit; 2001; 7(2):246-50. PubMed ID: 11257730
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mitochondrial
    Jiang Z; Teng L; Zhang S; Ding Y
    Mitochondrial DNA A DNA Mapp Seq Anal; 2021 Mar; 32(2):59-65. PubMed ID: 33284036
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome.
    Choo-Kang AT; Lynn S; Taylor GA; Daly ME; Sihota SS; Wardell TM; Chinnery PF; Turnbull DM; Walker M
    Diabetes; 2002 Jul; 51(7):2317-20. PubMed ID: 12086967
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular and clinical aspects of mitochondrial diabetes mellitus.
    Maassen JA; van Essen E; van den Ouweland JM; Lemkes HH
    Exp Clin Endocrinol Diabetes; 2001; 109(3):127-34. PubMed ID: 11409293
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M; Jiang P; Li F; Zhang J; Ji Y; He Y; Xu M; Zhu J; Meng X; Zhao F; Tong Y; Liu X; Sun Y; Zhou X; Mo JQ; Qu J; Guan MX
    Invest Ophthalmol Vis Sci; 2014 Mar; 55(3):1321-31. PubMed ID: 24398099
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Overexpressed mitochondrial leucyl-tRNA synthetase suppresses the A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Park H; Davidson E; King MP
    RNA; 2008 Nov; 14(11):2407-16. PubMed ID: 18796578
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Analysis of mitochondrial DNA gene tRNALeu(UUR) A3243G mutation in diabetic pedigrees].
    Wang CL; Li F; Hou QZ; Li HZ; Zhang Y; Ning G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):74-7. PubMed ID: 19199257
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P; Lee HC; Pang CY; Jeng CM; Huang SF; Wei YH
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Enhanced oxidative damage in human cells harboring A3243G mutation of mitochondrial DNA: implication of oxidative stress in the pathogenesis of mitochondrial diabetes.
    Pang CY; Lee HC; Wei YH
    Diabetes Res Clin Pract; 2001 Dec; 54 Suppl 2():S45-56. PubMed ID: 11733109
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Maternally transmitted diabetes mellitus may be associated with mitochondrial ND5 T12338C and tRNA
    Jiang Z; Cai X; Kong J; Zhang R; Ding Y
    Ir J Med Sci; 2022 Dec; 191(6):2625-2633. PubMed ID: 34993838
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA].
    Gál A; Szabó A; Pentelényi K; Pál Z
    Orv Hetil; 2008 Aug; 149(34):1593-8. PubMed ID: 18708313
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNA(Leu (UUR))) applied to a Norwegian family with diabetes mellitus and hearing loss.
    Akbari M; Skjelbred C; Følling I; Sagen J; Krokan HE
    Scand J Clin Lab Invest; 2004 Apr; 64(2):86-92. PubMed ID: 15115244
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mitochondrial gene mutations in the tRNA(Leu(UUR)) region and diabetes: prevalence and clinical phenotypes in Japan.
    Ohkubo K; Yamano A; Nagashima M; Mori Y; Anzai K; Akehi Y; Nomiyama R; Asano T; Urae A; Ono J
    Clin Chem; 2001 Sep; 47(9):1641-8. PubMed ID: 11514398
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The A3243G tRNALeu(UUR) mutation induces mitochondrial dysfunction and variable disease expression without dominant negative acting translational defects in complex IV subunits at UUR codons.
    Janssen GM; Hensbergen PJ; van Bussel FJ; Balog CI; Maassen JA; Deelder AM; Raap AK
    Hum Mol Genet; 2007 Oct; 16(20):2472-81. PubMed ID: 17656376
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees.
    Qiu Q; Li R; Jiang P; Xue L; Lu Y; Song Y; Han J; Lu Z; Zhi S; Mo JQ; Guan MX
    Hum Mutat; 2012 Aug; 33(8):1285-93. PubMed ID: 22549939
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy.
    Lu Y; Zhao D; Yao S; Wu S; Hong D; Wang Q; Liu J; Smeitink JAM; Yuan Y; Wang Z
    J Neurol Sci; 2017 Aug; 379():137-143. PubMed ID: 28716227
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.