224 related articles for article (PubMed ID: 9594306)
1. Mitochondrial tRNA(Leu(UUR)) gene mutation diabetes mellitus in Chinese.
Xiang K; Wang Y; Wu S; Lu H; Zheng T; Sun D; Weng Q; Jia W; Shen W; Pu L; He J
Chin Med J (Engl); 1997 May; 110(5):372-8. PubMed ID: 9594306
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
Ma L; Wang H; Chen J; Jin W; Liu L; Ban B; Shen J; Hua Z; Chai J
Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.
van den Ouweland JM; Lemkes HH; Ruitenbeek W; Sandkuijl LA; de Vijlder MF; Struyvenberg PA; van de Kamp JJ; Maassen JA
Nat Genet; 1992 Aug; 1(5):368-71. PubMed ID: 1284550
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Mitochondrial gene mutations that affect the binding of the termination factor and their prevalence among Japanese diabetes mellitus.
Odawara M; Asano M; Yamashita K
Nucleic Acids Symp Ser; 1995; (34):237-8. PubMed ID: 8841639
[TBL] [Abstract][Full Text] [Related]
8. Evaluation of the importance of maternal history of diabetes and of mitochondrial variation in the development of NIDDM.
McCarthy M; Cassell P; Tran T; Mathias L; 't Hart LM; Maassen JA; Snehalatha C; Ramachandran A; Viswanathan M; Hitman GA
Diabet Med; 1996 May; 13(5):420-8. PubMed ID: 8737023
[TBL] [Abstract][Full Text] [Related]
9. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
Xiu L; Zhang Q; Yu B
Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504
[TBL] [Abstract][Full Text] [Related]
10. Prevalence and clinical characteristics of mitochondrial tRNA leu(UUR) mt 3243 A-->G and ND-1 gene mt 3316 G-->A mutations in Chinese patients with type 2 diabetes.
Ji L; Hou X; Han X
Chin Med J (Engl); 2001 Nov; 114(11):1205-7. PubMed ID: 11729521
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region.
Tsukuda K; Suzuki Y; Kameoka K; Osawa N; Goto Y; Katagiri H; Asano T; Yazaki Y; Oka Y
Diabet Med; 1997 Dec; 14(12):1032-7. PubMed ID: 9455930
[TBL] [Abstract][Full Text] [Related]
13. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
Kameoka K; Isotani H; Tanaka K; Azukari K; Fujimura Y; Shiota Y; Sasaki E; Majima M; Furukawa K; Haginomori S; Kitaoka H; Ohsawa N
Biochem Biophys Res Commun; 1998 Apr; 245(2):523-7. PubMed ID: 9571188
[TBL] [Abstract][Full Text] [Related]
14. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
van den Ouweland JM; Lemkes HH; Trembath RC; Ross R; Velho G; Cohen D; Froguel P; Maassen JA
Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
Iwasaki N; Babazono T; Tsuchiya K; Tomonaga O; Suzuki A; Togashi M; Ujihara N; Sakka Y; Yokokawa H; Ogata M; Nihei H; Iwamoto Y
J Hum Genet; 2001; 46(6):330-4. PubMed ID: 11393536
[TBL] [Abstract][Full Text] [Related]
16. [Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].
Li W; Han D; Yuan H; Wang Y; Cao J; Yang W; Jiang S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb; 19(1):64-7. PubMed ID: 11836692
[TBL] [Abstract][Full Text] [Related]
17. Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases.
Mkaouar-Rebai E; Tlili A; Masmoudi S; Belguith N; Charfeddine I; Mnif M; Triki C; Fakhfakh F
Biochem Biophys Res Commun; 2007 Apr; 355(4):1031-7. PubMed ID: 17336924
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM
Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]