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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 9017352)

  • 1. UKPDS 21: low prevalence of the mitochondrial transfer RNA gene (tRNA(Leu(UUR))) mutation at position 3243bp in UK Caucasian type 2 diabetic patients.
    Saker PJ; Hattersley AT; Barrow B; Hammersley MS; Horton V; Gillmer MD; Turner RC
    Diabet Med; 1997 Jan; 14(1):42-5. PubMed ID: 9017352
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Kishimoto M; Hashiramoto M; Araki S; Ishida Y; Kazumi T; Kanda E; Kasuga M
    Diabetologia; 1995 Feb; 38(2):193-200. PubMed ID: 7713314
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.
    Katagiri H; Asano T; Ishihara H; Inukai K; Anai M; Yamanouchi T; Tsukuda K; Kikuchi M; Kitaoka H; Ohsawa N
    Diabetologia; 1994 May; 37(5):504-10. PubMed ID: 8056189
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The mitochondrial tRNA[Leu(UUR)] A to G 3243 mutation is associated with insulin-dependent and non-insulin-dependent diabetes in a Chinese population.
    Smith PR; Dronsfield MJ; Mijovic CH; Hattersley AT; Yeung VT; Cockram C; Chan JC; Barnett AH; Bain SC
    Diabet Med; 1997 Dec; 14(12):1026-31. PubMed ID: 9455929
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Mutation in the mitochondrial tRNA(leu) at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregnancies.
    Yanagisawa K; Uchigata Y; Sanaka M; Sakura H; Minei S; Shimizu M; Kanamuro R; Kadowaki T; Omori Y
    Diabetologia; 1995 Jul; 38(7):809-15. PubMed ID: 7556983
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Suzuki S; Hinokio Y; Hirai S; Onoda M; Matsumoto M; Ohtomo M; Kawasaki H; Satoh Y; Akai H; Abe K
    Diabetologia; 1994 Aug; 37(8):818-25. PubMed ID: 7988784
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene.
    Kadowaki T; Sakura H; Otabe S; Yasuda K; Kadowaki H; Mori Y; Hagura R; Akanuma Y; Yazaki Y
    Muscle Nerve Suppl; 1995; 3():S137-41. PubMed ID: 7603515
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Diminished insulin secretory response to glucose but normal insulin and glucagon secretory responses to arginine in a family with maternally inherited diabetes and deafness caused by mitochondrial tRNA(LEU(UUR)) gene mutation.
    Brändle M; Lehmann R; Maly FE; Schmid C; Spinas GA
    Diabetes Care; 2001 Jul; 24(7):1253-8. PubMed ID: 11423511
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutation.
    Suzuki Y; Suzuki S; Hinokio Y; Chiba M; Atsumi Y; Hosokawa K; Shimada A; Asahina T; Matsuoka K
    Diabetes Care; 1997 Jul; 20(7):1138-40. PubMed ID: 9203451
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Beta-cell loss and glucose induced signalling defects in diabetes mellitus caused by mitochondrial tRNALeu(UUR) gene mutation.
    Oka Y; Katagiri H; Ishihara H; Asano T; Kobayashi T; Kikuchi M
    Diabet Med; 1996 Sep; 13(9 Suppl 6):S98-102. PubMed ID: 8894492
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNA(Leu(UUR)) genes.
    Iwasaki N; Ohgawara H; Nagahara H; Kawamura M; Bell GI; Omori Y
    Acta Diabetol; 1995 Mar; 32(1):17-22. PubMed ID: 7542040
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
    Velho G; Byrne MM; Clément K; Sturis J; Pueyo ME; Blanché H; Vionnet N; Fiet J; Passa P; Robert JJ; Polonsky KS; Froguel P
    Diabetes; 1996 Apr; 45(4):478-87. PubMed ID: 8603770
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A patient with diabetes mellitus, cardiomyopathy, and a mitochondrial gene mutation: confirmation of a gene mutation in cardiac muscle.
    Kitaoka H; Kameoka K; Suzuki Y; Sasaki E; Majima M; Takada K; Katagiri H; Oka Y; Ohsawa N
    Diabetes Res Clin Pract; 1995 Jun; 28(3):207-12. PubMed ID: 8529500
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects.
    Fukuda M; Nakano S; Imaizumi N; Kitazawa M; Nishizawa M; Kigoshi T; Uchida K
    J Diabetes Complications; 1999; 13(5-6):277-83. PubMed ID: 10765002
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The clinical characteristics of patients with mitochondrial tRNA Leu(UUR)m.3243A > G mutation: Compared with type 1 diabetes and early onset type 2 diabetes.
    Zhu J; Yang P; Liu X; Yan L; Rampersad S; Li F; Li H; Sheng C; Cheng X; Zhang M; Qu S
    J Diabetes Complications; 2017 Aug; 31(8):1354-1359. PubMed ID: 28599824
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.