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 *

179 related articles for article (PubMed ID: 1677065)

  • 21. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W; Hayasaka K; Shoji Y; Takahashi T; Takada G; Saito M; Fukawa O; Wachi E
    Biochem Mol Biol Int; 1994 Aug; 33(6):1055-61. PubMed ID: 7804130
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy.
    Campos Y; Gámez J; García A; Andreu AL; Rubio JC; Martín MA; del Hoyo P; Navarro C; Cervera C; Garesse R; Arenas J
    Neuromuscul Disord; 2001 Jul; 11(5):477-80. PubMed ID: 11404120
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Multiple mitochondrial tRNA(Leu[UUR]) mutations associated with infantile myopathy.
    Zanssen S; Molnar M; Schröder JM; Buse G
    Mol Cell Biochem; 1997 Sep; 174(1-2):231-6. PubMed ID: 9309693
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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; 41(10):1786-96. PubMed ID: 12767666
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Diabetes mellitus and cardiomyopathy--association with mutation in the mitochondrial tRNA(Leu)(UUR) gene.
    Shiotani H; Ueno H; Inoue S; Yokota Y; Yokoyama M
    Jpn Circ J; 1998 Apr; 62(4):309-10. PubMed ID: 9583468
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mitochondrial myopathy with predominant respiratory dysfunction in a patient with A3243G mutation in the mitochondrial tRNA(Leu(UUR))gene.
    Yang CC; Hwang CC; Pang CY; Wei YH
    J Formos Med Assoc; 1998 Oct; 97(10):715-9. PubMed ID: 9830283
    [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. Variable distribution of mutant mitochondrial DNAs (tRNA(Leu[3243])) in tissues of symptomatic relatives with MELAS: the role of mitotic segregation.
    Macmillan C; Lach B; Shoubridge EA
    Neurology; 1993 Aug; 43(8):1586-90. PubMed ID: 8351017
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A patient with diabetes mellitus, cardiomyopathy, and a mitochondrial gene mutation: confirmation of a gene mutation in cardiac muscle.
    Kitaoka H; Kameoka K; Suzuki Y; Sasaki E; Majima M; Takada K; Katagiri H; Oka Y; Ohsawa N
    Diabetes Res Clin Pract; 1995 Jun; 28(3):207-12. PubMed ID: 8529500
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.
    Lu J; Wang D; Li R; Li W; Ji J; Zhao J; Ye W; Yang L; Qian Y; Zhu Y; Guan MX
    Biochem Biophys Res Commun; 2006 Sep; 348(1):115-9. PubMed ID: 16876129
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The Mitochondrial tRNALeu(UUR) A3302G Mutation may be Associated With Insulin Resistance in Woman With Polycystic Ovary Syndrome.
    Ding Y; Zhuo G; Zhang C
    Reprod Sci; 2016 Feb; 23(2):228-33. PubMed ID: 26335180
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy.
    Hsieh RH; Li JY; Pang CY; Wei YH
    J Biomed Sci; 2001; 8(4):328-35. PubMed ID: 11455195
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.
    Remes AM; Majamaa K; Herva R; Hassinen IE
    Neurology; 1993 May; 43(5):1015-20. PubMed ID: 8492919
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation.
    Park H; Davidson E; King MP
    Biochemistry; 2003 Feb; 42(4):958-64. PubMed ID: 12549915
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region.
    Tsukuda K; Suzuki Y; Kameoka K; Osawa N; Goto Y; Katagiri H; Asano T; Yazaki Y; Oka Y
    Diabet Med; 1997 Dec; 14(12):1032-7. PubMed ID: 9455930
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. OXPHOS defects and mitochondrial DNA mutations in cardiomyopathy.
    Zeviani M; Mariotti C; Antozzi C; Fratta GM; Rustin P; Prelle A
    Muscle Nerve Suppl; 1995; 3():S170-4. PubMed ID: 7603520
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L; Wang H; Chen J; Jin W; Liu L; Ban B; Shen J; Hua Z; Chai J
    Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.