114 related articles for article (PubMed ID: 15336535)
21. 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; 387(Pt 3):773-8. PubMed ID: 15554876
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Mitochondrial tRNA
Yang P; Wu P; Liu X; Feng J; Zheng S; Wang Y; Fan Z
Ir J Med Sci; 2020 May; 189(2):489-496. PubMed ID: 31776834
[TBL] [Abstract][Full Text] [Related]
25. Naturally occurring mutations in human mitochondrial pre-tRNASer(UCN) can affect the transfer ribonuclease Z cleavage site, processing kinetics, and substrate secondary structure.
Yan H; Zareen N; Levinger L
J Biol Chem; 2006 Feb; 281(7):3926-35. PubMed ID: 16361254
[TBL] [Abstract][Full Text] [Related]
26. [Mutation analysis of 12S rRNA and tRNA-Ser(UCN) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage].
Shu AL; Ji BH; Qin W; Feng GY; Nie YZ; Liu T; He L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):303-5. PubMed ID: 16767669
[TBL] [Abstract][Full Text] [Related]
27. Mitochondrial DNA base excision repair and mitochondrial DNA mutation in human hepatic HuH-7 cells exposed to stavudine.
Wu Y; Li N; Zhang T; Wu H; Huang C; Chen D
Mutat Res; 2009 May; 664(1-2):28-38. PubMed ID: 19428378
[TBL] [Abstract][Full Text] [Related]
28. Processing of human mitochondrial tRNA(Ser(AGY))GCU: a novel pathway in tRNA biosynthesis.
Rossmanith W
J Mol Biol; 1997 Jan; 265(4):365-71. PubMed ID: 9034356
[TBL] [Abstract][Full Text] [Related]
29. The precursor tRNA 3'-CCA interaction with Escherichia coli RNase P RNA is essential for catalysis by RNase P in vivo.
Wegscheid B; Hartmann RK
RNA; 2006 Dec; 12(12):2135-48. PubMed ID: 17135488
[TBL] [Abstract][Full Text] [Related]
30. Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation.
Reid FM; Rovio A; Holt IJ; Jacobs HT
Hum Mol Genet; 1997 Mar; 6(3):443-9. PubMed ID: 9147648
[TBL] [Abstract][Full Text] [Related]
31. Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction.
Hutchin TP; Navarro-Coy NC; Van Camp G; Tiranti V; Zeviani M; Schuelke M; Jaksch M; Newton V; Mueller RF
Eur J Hum Genet; 2001 May; 9(5):385-7. PubMed ID: 11378827
[TBL] [Abstract][Full Text] [Related]
32. In vivo and in vitro investigation of bacterial type B RNase P interaction with tRNA 3'-CCA.
Wegscheid B; Hartmann RK
Nucleic Acids Res; 2007; 35(6):2060-73. PubMed ID: 17355991
[TBL] [Abstract][Full Text] [Related]
33. The tRNA(Ser)-isoacceptors and their genes in Nicotiana rustica: genome organization, expression in vitro and sequence analyses.
Teichmann T; Urban C; Beier H
Plant Mol Biol; 1994 Mar; 24(6):889-901. PubMed ID: 8204826
[TBL] [Abstract][Full Text] [Related]
34. Functional conservation of tRNase ZL among Saccharomyces cerevisiae, Schizosaccharomyces pombe and humans.
Zhao Z; Su W; Yuan S; Huang Y
Biochem J; 2009 Aug; 422(3):483-92. PubMed ID: 19555350
[TBL] [Abstract][Full Text] [Related]
35. A tRNA(Ser)(UCN) gene in Artemia salina mitochondrial DNA: a case of mistaken identity.
Okimoto R; Wolstenholme DR
Curr Genet; 1993 Oct; 24(4):313-5. PubMed ID: 8252641
[TBL] [Abstract][Full Text] [Related]
36. Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation.
Schuelke M; Bakker M; Stoltenburg G; Sperner J; von Moers A
Ann Neurol; 1998 Oct; 44(4):700-4. PubMed ID: 9778273
[TBL] [Abstract][Full Text] [Related]
37. New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation.
Pulkes T; Liolitsa D; Eunson LH; Rose M; Nelson IP; Rahman S; Poulton J; Marchington DR; Landon DN; Debono AG; Morgan-Hughes JA; Hanna MG
Neuromuscul Disord; 2005 May; 15(5):364-71. PubMed ID: 15833431
[TBL] [Abstract][Full Text] [Related]
38. Processing and editing of overlapping tRNAs in human mitochondria.
Reichert A; Rothbauer U; Mörl M
J Biol Chem; 1998 Nov; 273(48):31977-84. PubMed ID: 9822669
[TBL] [Abstract][Full Text] [Related]
39. A novel cloverleaf structure found in mammalian mitochondrial tRNA(Ser) (UCN).
Yokogawa T; Watanabe Y; Kumazawa Y; Ueda T; Hirao I; Miura K; Watanabe K
Nucleic Acids Res; 1991 Nov; 19(22):6101-5. PubMed ID: 1840673
[TBL] [Abstract][Full Text] [Related]
40. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.
Kornblum C; Zsurka G; Wiesner RJ; Schröder R; Kunz WS
Biosci Rep; 2008 Apr; 28(2):89-96. PubMed ID: 18384291
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
