BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

362 related articles for article (PubMed ID: 33513266)

  • 21. Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.
    Kirino Y; Yasukawa T; Marjavaara SK; Jacobs HT; Holt IJ; Watanabe K; Suzuki T
    Hum Mol Genet; 2006 Mar; 15(6):897-904. PubMed ID: 16446307
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.
    James AM; Wei YH; Pang CY; Murphy MP
    Biochem J; 1996 Sep; 318 ( Pt 2)(Pt 2):401-7. PubMed ID: 8809026
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Import of several tRNAs from the cytoplasm into the mitochondria in bean Phaseolus vulgaris.
    Maréchal-Drouard L; Weil JH; Guillemaut P
    Nucleic Acids Res; 1988 Jun; 16(11):4777-88. PubMed ID: 3387208
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.
    Munakata K; Iwamoto K; Bundo M; Kato T
    Biol Psychiatry; 2005 Mar; 57(5):525-32. PubMed ID: 15737668
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sonlicromanol improves neuronal network dysfunction and transcriptome changes linked to m.3243A>G heteroplasmy in iPSC-derived neurons.
    Klein Gunnewiek TM; Verboven AHA; Pelgrim I; Hogeweg M; Schoenmaker C; Renkema H; Beyrath J; Smeitink J; de Vries BBA; Hoen PAC'; Kozicz T; Nadif Kasri N
    Stem Cell Reports; 2021 Sep; 16(9):2197-2212. PubMed ID: 34329596
    [TBL] [Abstract][Full Text] [Related]  

  • 26. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
    El-Hattab AW; Adesina AM; Jones J; Scaglia F
    Mol Genet Metab; 2015; 116(1-2):4-12. PubMed ID: 26095523
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M; Yabe I; Sudo A; Hosoki K; Yaguchi H; Saitoh S; Sasaki H
    J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Heterologous Inferential Analysis (HIA) and Other Emerging Concepts: In Understanding Mitochondrial Variation In Pathogenesis: There is no More Low-Hanging Fruit.
    Vila-Sanjurjo A; Smith PM; Elson JL
    Methods Mol Biol; 2021; 2277():203-245. PubMed ID: 34080154
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Impairment of tRNA processing by point mutations in mitochondrial tRNA(Leu)(UUR) associated with mitochondrial diseases.
    Rossmanith W; Karwan RM
    FEBS Lett; 1998 Aug; 433(3):269-74. PubMed ID: 9744809
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.
    Alila OF; Rebai EM; Tabebi M; Tej A; Chamkha I; Tlili A; Bouguila J; Tilouche S; Soyah N; Boughamoura L; Fakhfakh F
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul; 27(4):2873-80. PubMed ID: 26258512
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Chemical synthesis of the 5-taurinomethyl(-2-thio)uridine modified anticodon arm of the human mitochondrial tRNA(Leu(UUR)) and tRNA(Lys).
    Leszczynska G; Leonczak P; Wozniak K; Malkiewicz A
    RNA; 2014 Jun; 20(6):938-47. PubMed ID: 24757169
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutations.
    Tuppen HA; Fattori F; Carrozzo R; Zeviani M; DiMauro S; Seneca S; Martindale JE; Olpin SE; Treacy EP; McFarland R; Santorelli FM; Taylor RW
    J Med Genet; 2008 Jan; 45(1):55-61. PubMed ID: 18178636
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitochondrial tRNA mutations associated with deafness.
    Zheng J; Ji Y; Guan MX
    Mitochondrion; 2012 May; 12(3):406-13. PubMed ID: 22538251
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Exogenous peptides are able to penetrate human cell and mitochondrial membranes, stabilize mitochondrial tRNA structures, and rescue severe mitochondrial defects.
    Perli E; Pisano A; Pignataro MG; Campese AF; Pelullo M; Genovese I; de Turris V; Ghelli AM; Cerbelli B; Giordano C; Colotti G; Morea V; d'Amati G
    FASEB J; 2020 Jun; 34(6):7675-7686. PubMed ID: 32304340
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELAS.
    Desquiret-Dumas V; Gueguen N; Barth M; Chevrollier A; Hancock S; Wallace DC; Amati-Bonneau P; Henrion D; Bonneau D; Reynier P; Procaccio V
    Biochim Biophys Acta; 2012 Jun; 1822(6):1019-29. PubMed ID: 22306605
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The pathogenic U3271C human mitochondrial tRNA(Leu(UUR)) mutation disrupts a fragile anticodon stem.
    Wittenhagen LM; Roy MD; Kelley SO
    Nucleic Acids Res; 2003 Jan; 31(2):596-601. PubMed ID: 12527767
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming.
    Picard M; Zhang J; Hancock S; Derbeneva O; Golhar R; Golik P; O'Hearn S; Levy S; Potluri P; Lvova M; Davila A; Lin CS; Perin JC; Rappaport EF; Hakonarson H; Trounce IA; Procaccio V; Wallace DC
    Proc Natl Acad Sci U S A; 2014 Sep; 111(38):E4033-42. PubMed ID: 25192935
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Presentation of m.3243A>G (MT-TL1; tRNALeu) variant with focal neurology in infancy.
    Mordaunt DA; McIntyre LC; Salvemini H; Ibrahim A; Bratkovic D; Ketteridge D; Scott HS; Kassahn KS; Smith N
    Am J Med Genet A; 2015 Nov; 167A(11):2697-701. PubMed ID: 26289840
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
    Jean-Francois MJ; Lertrit P; Berkovic SF; Crimmins D; Morris J; Marzuki S; Byrne E
    Aust N Z J Med; 1994 Apr; 24(2):188-93. PubMed ID: 8042948
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.