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.
407 related articles for article (PubMed ID: 16199753)
21. 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; 14(7):417-20. PubMed ID: 15210164 [TBL] [Abstract][Full Text] [Related]
22. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis. Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222 [TBL] [Abstract][Full Text] [Related]
23. Nuclear control of cloverleaf structure of human mitochondrial tRNA(Lys). Helm M; Attardi G J Mol Biol; 2004 Mar; 337(3):545-60. PubMed ID: 15019776 [TBL] [Abstract][Full Text] [Related]
24. Mytilus mitochondrial DNA contains a functional gene for a tRNASer(UCN) with a dihydrouridine arm-replacement loop and a pseudo-tRNASer(UCN) gene. Beagley CT; Okimoto R; Wolstenholme DR Genetics; 1999 Jun; 152(2):641-52. PubMed ID: 10353906 [TBL] [Abstract][Full Text] [Related]
25. Interdomain communication between weak structural elements within a disease-related human tRNA. Roy MD; Wittenhagen LM; Vozzella BE; Kelley SO Biochemistry; 2004 Jan; 43(2):384-92. PubMed ID: 14717592 [TBL] [Abstract][Full Text] [Related]
26. Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs. Suzuki T; Nagao A; Suzuki T Wiley Interdiscip Rev RNA; 2011; 2(3):376-86. PubMed ID: 21957023 [TBL] [Abstract][Full Text] [Related]
27. A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagia. Souilem S; Kefi M; Mancuso M; Nesti C; Hentati F; Amouri R Diagn Mol Pathol; 2010 Mar; 19(1):28-32. PubMed ID: 20186009 [TBL] [Abstract][Full Text] [Related]
28. Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNA ser(UCN) gene. Cardaioli E; Da Pozzo P; Cerase A; Sicurelli F; Malandrini A; De Stefano N; Stromillo ML; Battisti C; Dotti MT; Federico A Neuromuscul Disord; 2006 Jan; 16(1):26-31. PubMed ID: 16368237 [TBL] [Abstract][Full Text] [Related]
30. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss. Jin L; Yang A; Zhu Y; Zhao J; Wang X; Yang L; Sun D; Tao Z; Tsushima A; Wu G; Xu L; Chen C; Yi B; Cai J; Tang X; Wang J; Li D; Yuan Q; Liao Z; Chen J; Li Z; Lu J; Guan MX Biochem Biophys Res Commun; 2007 Sep; 361(1):133-9. PubMed ID: 17659260 [TBL] [Abstract][Full Text] [Related]
31. Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybrids. Toompuu M; Tiranti V; Zeviani M; Jacobs HT Hum Mol Genet; 1999 Nov; 8(12):2275-83. PubMed ID: 10545608 [TBL] [Abstract][Full Text] [Related]
32. The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients. Rydzanicz M; Cywińska K; Wróbel M; Pollak A; Gawęcki W; Wojsyk-Banaszak I; Lechowicz U; Mueller-Malesińska M; Ołdak M; Płoski R; Skarżyński H; Szyfter K; Szyfter W Mol Genet Metab; 2011; 104(1-2):153-9. PubMed ID: 21621438 [TBL] [Abstract][Full Text] [Related]
33. Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNA Fan W; Zheng J; Kong W; Cui L; Aishanjiang M; Yi Q; Wang M; Cang X; Tang X; Chen Y; Mo JQ; Sondheimer N; Ge W; Guan MX J Biol Chem; 2019 Dec; 294(50):19292-19305. PubMed ID: 31685661 [TBL] [Abstract][Full Text] [Related]
34. Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy. Mariotti C; Tiranti V; Carrara F; Dallapiccola B; DiDonato S; Zeviani M J Clin Invest; 1994 Mar; 93(3):1102-7. PubMed ID: 8132749 [TBL] [Abstract][Full Text] [Related]
35. Bovine mitochondrial tRNAPhe, tRNASer (AGY) and tRNASer (UCN): preparation using a new detection method and their properties in aminoacylation. Kumazawa Y; Yokogawa T; Miura K; Watanabe K Nucleic Acids Symp Ser; 1988; (19):97-100. PubMed ID: 3226927 [TBL] [Abstract][Full Text] [Related]
36. A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment. Hutchin TP; Parker MJ; Young ID; Davis AC; Pulleyn LJ; Deeble J; Lench NJ; Markham AF; Mueller RF J Med Genet; 2000 Sep; 37(9):692-4. PubMed ID: 10978361 [TBL] [Abstract][Full Text] [Related]
37. Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease. Yasukawa T; Suzuki T; Ishii N; Ohta S; Watanabe K EMBO J; 2001 Sep; 20(17):4794-802. PubMed ID: 11532943 [TBL] [Abstract][Full Text] [Related]
39. Human mitochondrial tRNA quality control in health and disease: a channelling mechanism? Belostotsky R; Frishberg Y; Entelis N RNA Biol; 2012 Jan; 9(1):33-9. PubMed ID: 22258151 [TBL] [Abstract][Full Text] [Related]