BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 8894492)

  • 1. 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]  

  • 2. Mitochondrial diabetes mellitus--glucose-induced signaling defects and beta-cell loss.
    Oka Y; Katagiri H; Ishihara H; Asano T; Kikuchi M; Kobayashi T
    Muscle Nerve Suppl; 1995; 3():S131-6. PubMed ID: 7603514
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene.
    Iwasaki N; Wasada T; Takahashi Y; Babazono T; Ohgawara H; Omori Y
    Diabetes Care; 1995 Jun; 18(6):886-8. PubMed ID: 7555525
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Unpleasant alcohol effect in diabetes associated with 3243 bp mitochondrial tRNALeu(UUR) mutation.
    Suzuki Y; Atsumi Y; Hosokawa K; Taniyama M; Kadowaki T; Oka Y; Tanaka Y; Asahina T; Matsuoka K
    Diabetes Care; 1995 Jun; 18(6):880-1. PubMed ID: 7555519
    [No Abstract]   [Full Text] [Related]  

  • 10. Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene.
    Odawara M; Sasaki K; Yamashita K
    J Clin Endocrinol Metab; 1995 Apr; 80(4):1290-4. PubMed ID: 7714102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Relationship between insulin-dependent diabetes mellitus (IDDM) and non-insulin-dependent diabetes mellitus: beta-cell function, islet cell antibody, and haptoglobin in parents of IDDM patients.
    Kajio H; Kobayashi T; Nakanishi K; Okubo M; Tsukada T; Nakayama T; Yamada N; Murase T; Yazaki Y; Kosaka K
    Metabolism; 1995 Jul; 44(7):869-75. PubMed ID: 7616845
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Genetic diagnosis of a subtype diabetes mellitus with mitochondrial tRNA Leu(UUR) gene mutation].
    Xiang K; Lu H; Wu S
    Zhonghua Yi Xue Za Zhi; 1995 Apr; 75(4):216-9, 255. PubMed ID: 7540496
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
    Gerbitz KD; Paprotta A; Jaksch M; Zierz S; Drechsel J
    FEBS Lett; 1993 Apr; 321(2-3):194-6. PubMed ID: 8477849
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 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. Clinical and laboratory characteristics in the families with diabetes and a mitochondrial tRNA(LEU(UUR)) gene mutation.
    Iwanishi M; Obata T; Yamada S; Maegawa H; Tachikawa-Ide R; Ugi S; Hasegawa M; Kojima H; Oguni T; Toudo R
    Diabetes Res Clin Pract; 1995 Aug; 29(2):75-82. PubMed ID: 8591702
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NIDDM--genetic marker; glucose transporter, glucokinase, and mitochondria gene.
    Oka Y
    Diabetes Res Clin Pract; 1994 Oct; 24 Suppl():S117-21. PubMed ID: 7859592
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics.
    Oka Y; Katagiri H; Yazaki Y; Murase T; Kobayashi T
    Lancet; 1993 Aug; 342(8870):527-8. PubMed ID: 8102670
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.