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 *

343 related articles for article (PubMed ID: 1354782)

  • 21. Maturity-onset diabetes of the young (MODY), MODY genes and non-insulin-dependent diabetes mellitus.
    Velho G; Froguel P
    Diabetes Metab; 1997 Mar; 23 Suppl 2():34-7. PubMed ID: 9162575
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Nonsense mutation of glucokinase gene in late-onset non-insulin-dependent diabetes mellitus.
    Katagiri H; Asano T; Ishihara H; Inukai K; Anai M; Miyazaki J; Tsukuda K; Kikuchi M; Yazaki Y; Oka Y
    Lancet; 1992 Nov; 340(8831):1316-7. PubMed ID: 1360036
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Glucokinase, the pancreatic glucose sensor, is not the gut glucose sensor.
    Murphy R; Tura A; Clark PM; Holst JJ; Mari A; Hattersley AT
    Diabetologia; 2009 Jan; 52(1):154-9. PubMed ID: 18974968
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Glucokinase mutations, insulin secretion, and diabetes mellitus.
    Bell GI; Pilkis SJ; Weber IT; Polonsky KS
    Annu Rev Physiol; 1996; 58():171-86. PubMed ID: 8815790
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.
    Byrne MM; Sturis J; Menzel S; Yamagata K; Fajans SS; Dronsfield MJ; Bain SC; Hattersley AT; Velho G; Froguel P; Bell GI; Polonsky KS
    Diabetes; 1996 Nov; 45(11):1503-10. PubMed ID: 8866553
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Role of common sequence variants in insulin secretion in familial type 2 diabetic kindreds: the sulfonylurea receptor, glucokinase, and hepatocyte nuclear factor 1alpha genes.
    Elbein SC; Sun J; Scroggin E; Teng K; Hasstedt SJ
    Diabetes Care; 2001 Mar; 24(3):472-8. PubMed ID: 11289470
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. The effect of glimepiride on pancreatic beta-cell function under hyperglycaemic clamp and hyperinsulinaemic, euglycaemic clamp conditions in non-insulin-dependent diabetes mellitus.
    Clark HE; Matthews DR
    Horm Metab Res; 1996 Sep; 28(9):445-50. PubMed ID: 8911981
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The genetic abnormality in the beta cell determines the response to an oral glucose load.
    Stride A; Vaxillaire M; Tuomi T; Barbetti F; Njølstad PR; Hansen T; Costa A; Conget I; Pedersen O; Søvik O; Lorini R; Groop L; Froguel P; Hattersley AT
    Diabetologia; 2002 Mar; 45(3):427-35. PubMed ID: 11914749
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Maturity-onset diabetes of the young--MODY. Molecular-genetic, pathophysiological and clinical characteristics].
    Hansen T; Urhammer SA; Pedersen OB
    Ugeskr Laeger; 2002 Apr; 164(15):2017-22. PubMed ID: 11984998
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Phenotype Heterogeneity in Glucokinase-Maturity-Onset Diabetes of the Young (GCK-MODY) Patients.
    Wędrychowicz A; Tobór E; Wilk M; Ziółkowska-Ledwith E; Rams A; Wzorek K; Sabal B; Stelmach M; Starzyk JB
    J Clin Res Pediatr Endocrinol; 2017 Sep; 9(3):246-252. PubMed ID: 28663157
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Glucokinase-maturity onset diabetes mellitus in the young suggested by factory-calibrated glucose monitoring data: a case report.
    Nomura N; Iizuka K; Goshima E; Hosomichi K; Tajima A; Kubota S; Liu Y; Takao K; Kato T; Mizuno M; Hirota T; Suwa T; Horikawa Y; Yabe D
    Endocr J; 2022 Apr; 69(4):473-477. PubMed ID: 34803122
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Glucokinase mutations in pediatric patients with impaired fasting glucose.
    Aloi C; Salina A; Minuto N; Tallone R; Lugani F; Mascagni A; Mazza O; Cassanello M; Maghnie M; d'Annunzio G
    Acta Diabetol; 2017 Oct; 54(10):913-923. PubMed ID: 28726111
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular and clinical characterization of glucokinase maturity-onset diabetes of the young (GCK-MODY) in Japanese patients.
    Kawakita R; Hosokawa Y; Fujimaru R; Tamagawa N; Urakami T; Takasawa K; Moriya K; Mizuno H; Maruo Y; Takuwa M; Nagasaka H; Nishi Y; Yamamoto Y; Aizu K; Yorifuji T
    Diabet Med; 2014 Nov; 31(11):1357-62. PubMed ID: 24804978
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Glucokinase gene islet promoter region variant (G-->A) at nucleotide -30 is not associated with reduced insulin secretion in Finns.
    Rissanen J; Saarinen L; Heikkinen S; Kekäläinen P; Mykkänen L; Kuusisto J; Deeb SS; Laakso M
    Diabetes Care; 1998 Jul; 21(7):1194-7. PubMed ID: 9653619
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
    Vionnet N; Stoffel M; Takeda J; Yasuda K; Bell GI; Zouali H; Lesage S; Velho G; Iris F; Passa P
    Nature; 1992 Apr; 356(6371):721-2. PubMed ID: 1570017
    [TBL] [Abstract][Full Text] [Related]  

  • 37. GCK-MODY diabetes as a protein misfolding disease: the mutation R275C promotes protein misfolding, self-association and cellular degradation.
    Negahdar M; Aukrust I; Molnes J; Solheim MH; Johansson BB; Sagen JV; Dahl-Jørgensen K; Kulkarni RN; Søvik O; Flatmark T; Njølstad PR; Bjørkhaug L
    Mol Cell Endocrinol; 2014 Jan; 382(1):55-65. PubMed ID: 24001579
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Glucokinase gene abnormalities in maturity-onset diabetes of the young (MODY) and late-onset NIDDM].
    Odawara M
    Nihon Rinsho; 1994 Oct; 52(10):2580-6. PubMed ID: 7983782
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation.
    Chakera AJ; Steele AM; Gloyn AL; Shepherd MH; Shields B; Ellard S; Hattersley AT
    Diabetes Care; 2015 Jul; 38(7):1383-92. PubMed ID: 26106223
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree.
    Herman WH; Fajans SS; Ortiz FJ; Smith MJ; Sturis J; Bell GI; Polonsky KS; Halter JB
    Diabetes; 1994 Jan; 43(1):40-6. PubMed ID: 8262315
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.