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.
171 related articles for article (PubMed ID: 18417955)
1. Markedly different clinical features in 2 diabetes mellitus patients with extremely high tissue levels of the mitochondrial DNA A3243G mutation. Harihara S; Nakamura K; Fujiwara M; Arai T; Sawabe M; Takeuchi F; Takubo K Gerontology; 2008; 54(3):168-72. PubMed ID: 18417955 [TBL] [Abstract][Full Text] [Related]
2. [A case of mitochondrial encephalomyopathy showing ophthalmoplegia, diabetes mellitus and hearing loss associated with the A3243G mutation of mitochondrial DNA]. Hoshino S; Tamaoka A; Ohkoshi N; Shoji S; Goto Y Rinsho Shinkeigaku; 1997 Apr; 37(4):326-30. PubMed ID: 9248343 [TBL] [Abstract][Full Text] [Related]
3. Search for mitochondrial A3243G tRNA(Leu) mutation in Polish patients with type 2 diabetes mellitus. Małecki M; Klupa T; Wanic K; Frey J; Cyganek K; Sieradzki J Med Sci Monit; 2001; 7(2):246-50. PubMed ID: 11257730 [TBL] [Abstract][Full Text] [Related]
4. A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness. Chen FL; Liu Y; Song XY; Hu HY; Xu HB; Zhang XM; Shi JH; Hu J; Shen Y; Lu B; Wang XC; Hu RM Mutat Res; 2006 Dec; 602(1-2):26-33. PubMed ID: 16949108 [TBL] [Abstract][Full Text] [Related]
5. [Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case]. Biarnés J; Barrientos A; Ricart W; Nunes V; Fernández-Castañer M; Soler J Med Clin (Barc); 1999 Jan; 112(3):99-101. PubMed ID: 10074618 [TBL] [Abstract][Full Text] [Related]
6. Nonrandom tissue distribution of mutant mtDNA. Chinnery PF; Zwijnenburg PJ; Walker M; Howell N; Taylor RW; Lightowlers RN; Bindoff L; Turnbull DM Am J Med Genet; 1999 Aug; 85(5):498-501. PubMed ID: 10405450 [TBL] [Abstract][Full Text] [Related]
7. The level of the mitochondrial mutation A3243G decreases upon ageing in epithelial cells from individuals with diabetes and deafness. Olsson C; Johnsen E; Nilsson M; Wilander E; Syvänen AC; Lagerström-Fermér M Eur J Hum Genet; 2001 Dec; 9(12):917-21. PubMed ID: 11840193 [TBL] [Abstract][Full Text] [Related]
8. [Mitochondrial DNA 3243, 3316 point mutations and type 2 diabetes mellitus]. Tang J; Li J; Tian X; Kong Q; Zhang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):198-200. PubMed ID: 15793785 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Level of heteroplasmy for the mitochondrial mutation A3243G correlates with age at onset of diabetes and deafness. Olsson C; Zethelius B; Lagerström-Fermér M; Asplund J; Berne C; Landegren U Hum Mutat; 1998; 12(1):52-8. PubMed ID: 9633820 [TBL] [Abstract][Full Text] [Related]
11. A pilot study of mitochondrial DNA point mutation A3243G in a sample of Croatian patients having type 2 diabetes mellitus associated with maternal inheritance. Martin-Kleiner I; Pape-Medvidović E; Pavlić-Renar I; Metelko Z; Kusec R; Gabrilovac J; Boranić M Acta Diabetol; 2004 Dec; 41(4):179-84. PubMed ID: 15660201 [TBL] [Abstract][Full Text] [Related]
12. [Study on mitochondrial DNA gene tRNA(Leu(UUR)) A3243G mutation in type 2 diabetes mellitus]. Zhang XY; Zhang SL; Ke BS; Jiang ZS; Sun R Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):168-70. PubMed ID: 15079803 [TBL] [Abstract][Full Text] [Related]
13. Mitochondrial DNA abnormalities and autistic spectrum disorders. Pons R; Andreu AL; Checcarelli N; Vilà MR; Engelstad K; Sue CM; Shungu D; Haggerty R; de Vivo DC; DiMauro S J Pediatr; 2004 Jan; 144(1):81-5. PubMed ID: 14722523 [TBL] [Abstract][Full Text] [Related]
14. Distinct nuclear gene expression profiles in cells with mtDNA depletion and homoplasmic A3243G mutation. Jahangir Tafrechi RS; Svensson PJ; Janssen GM; Szuhai K; Maassen JA; Raap AK Mutat Res; 2005 Oct; 578(1-2):43-52. PubMed ID: 16202796 [TBL] [Abstract][Full Text] [Related]
15. Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo. Chinnery PF; Taylor DJ; Brown DT; Manners D; Styles P; Lodi R Ann Neurol; 2000 Mar; 47(3):381-4. PubMed ID: 10716261 [TBL] [Abstract][Full Text] [Related]
16. Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis. Verny C; Amati-Bonneau P; Letournel F; Person B; Dib N; Malinge MC; Slama A; Le Maréchal C; Ferec C; Procaccio V; Reynier P; Bonneau D Diabetes Metab; 2008 Dec; 34(6 Pt 1):620-6. PubMed ID: 18955007 [TBL] [Abstract][Full Text] [Related]
17. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation]. Zhang Y; Wang ZX; Niu SL; Xu YF; Pei P; Yuan Y; Yang YL; Qi Y Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb; 27(1):77-80. PubMed ID: 15782498 [TBL] [Abstract][Full Text] [Related]
18. [Development of a DNA chip screening mitochondrial DNA mutations in patients with diabetes mellitus]. Liu SM; Zhou X; Zheng F; Li X; Qin H; Zhang HM; Li D Zhonghua Yi Xue Za Zhi; 2006 Oct; 86(40):2853-7. PubMed ID: 17200023 [TBL] [Abstract][Full Text] [Related]
19. [Analysis of mitochondrial DNA gene tRNALeu(UUR) A3243G mutation in diabetic pedigrees]. Wang CL; Li F; Hou QZ; Li HZ; Zhang Y; Ning G Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):74-7. PubMed ID: 19199257 [TBL] [Abstract][Full Text] [Related]
20. [Study on the mitochondrial DNA variation in patients with type 2 diabetes mellitus]. Ji JZ; Lu JX; Ye W; Hu X; Wang DW Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Apr; 24(2):167-72. PubMed ID: 17407074 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]