161 related articles for article (PubMed ID: 15694374)
41. 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]
42. 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]
43. Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Bonora E; Porcelli AM; Gasparre G; Biondi A; Ghelli A; Carelli V; Baracca A; Tallini G; Martinuzzi A; Lenaz G; Rugolo M; Romeo G
Cancer Res; 2006 Jun; 66(12):6087-96. PubMed ID: 16778181
[TBL] [Abstract][Full Text] [Related]
44. Enhanced ROS production and antioxidant defenses in cybrids harbouring mutations in mtDNA.
Vives-Bauza C; Gonzalo R; Manfredi G; Garcia-Arumi E; Andreu AL
Neurosci Lett; 2006 Jan; 391(3):136-41. PubMed ID: 16165271
[TBL] [Abstract][Full Text] [Related]
45. Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.
Xing G; Chen Z; Wei Q; Tian H; Li X; Zhou A; Bu X; Cao X
Biochem Biophys Res Commun; 2006 Aug; 346(4):1131-5. PubMed ID: 16782057
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.
Wang M; Peng Y; Zheng J; Zheng B; Jin X; Liu H; Wang Y; Tang X; Huang T; Jiang P; Guan MX
Nucleic Acids Res; 2016 Dec; 44(22):10974-10985. PubMed ID: 27536005
[TBL] [Abstract][Full Text] [Related]
48. Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene.
Sue CM; Tanji K; Hadjigeorgiou G; Andreu AL; Nishino I; Krishna S; Bruno C; Hirano M; Shanske S; Bonilla E; Fischel-Ghodsian N; DiMauro S; Friedman R
Neurology; 1999 Jun; 52(9):1905-8. PubMed ID: 10371545
[TBL] [Abstract][Full Text] [Related]
49. Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss.
Tang X; Zheng J; Ying Z; Cai Z; Gao Y; He Z; Yu H; Yao J; Yang Y; Wang H; Chen Y; Guan MX
Mitochondrion; 2015 Jul; 23():17-24. PubMed ID: 25968158
[TBL] [Abstract][Full Text] [Related]
50. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.
Wang Q; Li QZ; Han D; Zhao Y; Zhao L; Qian Y; Yuan H; Li R; Zhai S; Young WY; Guan MX
Biochem Biophys Res Commun; 2006 Feb; 340(2):583-8. PubMed ID: 16380089
[TBL] [Abstract][Full Text] [Related]
51. Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.
Gutiérrez Cortés N; Pertuiset C; Dumon E; Börlin M; Hebert-Chatelain E; Pierron D; Feldmann D; Jonard L; Marlin S; Letellier T; Rocher C
Hum Mutat; 2012 Apr; 33(4):681-9. PubMed ID: 22241583
[TBL] [Abstract][Full Text] [Related]
52. Low penetrance of hearing loss in two Chinese families carrying the mitochondrial tRNASer(UCN) mutations.
Peng W; Zhong Y; Zhao X; Yuan J
Mol Med Rep; 2020 Jul; 22(1):77-86. PubMed ID: 32377700
[TBL] [Abstract][Full Text] [Related]
53. Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene.
Tiranti V; Chariot P; Carella F; Toscano A; Soliveri P; Girlanda P; Carrara F; Fratta GM; Reid FM; Mariotti C; Zeviani M
Hum Mol Genet; 1995 Aug; 4(8):1421-7. PubMed ID: 7581383
[TBL] [Abstract][Full Text] [Related]
54. 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]
55. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
[TBL] [Abstract][Full Text] [Related]
56. 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]
57. Asymmetrical effects of deafness-associated mitochondrial DNA 7516delA mutation on the processing of RNAs in the H-strand and L-strand polycistronic transcripts.
Xiao Y; Wang M; He Q; Xu L; Zhang Q; Meng F; Jia Z; Zhang F; Wang H; Guan MX
Nucleic Acids Res; 2020 Nov; 48(19):11113-11129. PubMed ID: 33045734
[TBL] [Abstract][Full Text] [Related]
58. A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual loss.
Mkaouar-Rebai E; Chamkha I; Kammoun T; Alila-Fersi O; Aloulou H; Hachicha M; Fakhfakh F
Biochem Biophys Res Commun; 2013 Jan; 430(2):585-91. PubMed ID: 23219819
[TBL] [Abstract][Full Text] [Related]
59. In vitro 3'-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness.
Levinger L; Jacobs O; James M
Nucleic Acids Res; 2001 Nov; 29(21):4334-40. PubMed ID: 11691920
[TBL] [Abstract][Full Text] [Related]
60. Sequence analysis of the mitochondrial genome from a large family with maternally inherited nonsyndromic deafness.
Zhang HJ; Xu CH; Zhan YJ; Zhao SY; Shan YF; Geng XX; Shan XN
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):368-71. PubMed ID: 16086269
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
