BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 7603513)

  • 1. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
    van den Ouweland JM; Lemkes HH; Gerbitz KD; Maassen JA
    Muscle Nerve Suppl; 1995; 3():S124-30. PubMed ID: 7603513
    [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. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L; Caruso RA; Zuccarello D; Rigoli M; Barberi I
    Diabetes Nutr Metab; 2001 Dec; 14(6):343-8. PubMed ID: 11853367
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.
    van den Ouweland JM; Maechler P; Wollheim CB; Attardi G; Maassen JA
    Diabetologia; 1999 Apr; 42(4):485-92. PubMed ID: 10230654
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
    Newkirk JE; Taylor RW; Howell N; Bindoff LA; Chinnery PF; Alberti KG; Turnbull DM; Walker M
    Diabet Med; 1997 Jun; 14(6):457-60. PubMed ID: 9212310
    [TBL] [Abstract][Full Text] [Related]  

  • 8. D-glucose metabolism in lymphocytes of patients with mitochondrial point mutation of the tRNALeu(UUR) gene.
    Malaisse WJ; Pueyo ME; Nadi AB; Malaisse-Lagae F; Froguel P; Velho G
    Biochem Mol Med; 1995 Apr; 54(2):91-5. PubMed ID: 8581364
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.
    Bergamin CS; Rolim LC; Dib SA; Moisés RS
    Arq Bras Endocrinol Metabol; 2008 Nov; 52(8):1345-9. PubMed ID: 19169492
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.
    Manouvrier S; Rötig A; Hannebique G; Gheerbrandt JD; Royer-Legrain G; Munnich A; Parent M; Grünfeld JP; Largilliere C; Lombes A
    J Med Genet; 1995 Aug; 32(8):654-6. PubMed ID: 7473662
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Accelerated cardiomyopathy in maternally inherited diabetes and deafness.
    Mangiafico RA; Zeviani M; Bartoloni G; Fiore CE
    Int J Clin Pharmacol Res; 2004; 24(1):15-21. PubMed ID: 15575173
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene.
    Awata T; Matsumoto T; Iwamoto Y; Matsuda A; Kuzuya T; Saito T
    Lancet; 1993 May; 341(8855):1291-2. PubMed ID: 8098444
    [No Abstract]   [Full Text] [Related]  

  • 14. [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]  

  • 15. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ; Mudde AH; 't Hart LM; Huygen PL; Cremers CW
    Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus.
    Shigemoto M; Yoshimasa Y; Yamamoto Y; Hayashi T; Suga J; Inoue G; Okamoto M; Jingami H; Tsuda K; Yamamoto T; Yagura T; Oishi M; Tsujii S; Kuzuya H; Nakao K
    Intern Med; 1998 Mar; 37(3):265-72. PubMed ID: 9617861
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.
    Maassen JA; van den Ouweland JM; t Hart LM; Lemkes HH
    Horm Metab Res; 1997 Feb; 29(2):50-5. PubMed ID: 9105898
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S; Hinokio Y; Ohtomo M; Hirai M; Hirai A; Chiba M; Kasuga S; Satoh Y; Akai H; Toyota T
    Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular and clinical aspects of mitochondrial diabetes mellitus.
    Maassen JA; van Essen E; van den Ouweland JM; Lemkes HH
    Exp Clin Endocrinol Diabetes; 2001; 109(3):127-34. PubMed ID: 11409293
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.