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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

134 related items for PubMed ID: 6312455

  • 21. Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations.
    Kapoor RR, Locke J, Colclough K, Wales J, Conn JJ, Hattersley AT, Ellard S, Hussain K.
    Diabetes; 2008 Jun; 57(6):1659-63. PubMed ID: 18268044
    [Abstract] [Full Text] [Related]

  • 22. 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 23; 356(6371):721-2. PubMed ID: 1570017
    [Abstract] [Full Text] [Related]

  • 23. [Investigation of the insulin gene by the amplification method in vitro].
    Horst-Sikorska W, Krzyzagórska E, Chlebowska H.
    Endokrynol Pol; 1992 Apr 23; 43(1):31-7. PubMed ID: 1345523
    [Abstract] [Full Text] [Related]

  • 24. MODY in Iceland is associated with mutations in HNF-1alpha and a novel mutation in NeuroD1.
    Kristinsson SY, Thorolfsdottir ET, Talseth B, Steingrimsson E, Thorsson AV, Helgason T, Hreidarsson AB, Arngrimsson R.
    Diabetologia; 2001 Nov 23; 44(11):2098-103. PubMed ID: 11719843
    [Abstract] [Full Text] [Related]

  • 25. Prolonged episodes of hypoglycaemia in HNF4A-MODY mutation carriers with IGT. Evidence of persistent hyperinsulinism into early adulthood.
    Bacon S, Kyithar MP, Condron EM, Vizzard N, Burke M, Byrne MM.
    Acta Diabetol; 2016 Dec 23; 53(6):965-972. PubMed ID: 27552834
    [Abstract] [Full Text] [Related]

  • 26. Loss of a restriction endonuclease cleavage site in the gene of a structurally abnormal human insulin.
    Kwok SC, Chan SJ, Rubenstein AH, Poucher R, Steiner DF.
    Biochem Biophys Res Commun; 1981 Feb 12; 98(3):844-9. PubMed ID: 6261753
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Analysis of the gene sequences of the insulin receptor and the insulin-sensitive glucose transporter (GLUT-4) in patients with common-type non-insulin-dependent diabetes mellitus.
    Kusari J, Verma US, Buse JB, Henry RR, Olefsky JM.
    J Clin Invest; 1991 Oct 12; 88(4):1323-30. PubMed ID: 1918382
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Review for clinical molecular genetics of mutant insulin].
    Sanke T, Nanjo K.
    Nihon Rinsho; 1994 Oct 12; 52(10):2550-5. PubMed ID: 7983776
    [Abstract] [Full Text] [Related]

  • 31. Three mutant insulins in man.
    Shoelson S, Haneda M, Blix P, Nanjo A, Sanke T, Inouye K, Steiner D, Rubenstein A, Tager H.
    Nature; 1983 Apr 07; 302(5908):540-3. PubMed ID: 6339950
    [Abstract] [Full Text] [Related]

  • 32. Hyperinsulinemic hypoglycemia syndrome associated with mutations in the human insulin receptor gene: report of two cases.
    Kuroda Y, Iwahashi H, Mineo I, Fukui K, Fukuhara A, Iwamoto R, Imagawa A, Shimomura I.
    Endocr J; 2015 Apr 07; 62(4):353-62. PubMed ID: 25753915
    [Abstract] [Full Text] [Related]

  • 33. Genetics of type 2 diabetes mellitus.
    Malecki MT.
    Diabetes Res Clin Pract; 2005 Jun 07; 68 Suppl1():S10-21. PubMed ID: 15955369
    [Abstract] [Full Text] [Related]

  • 34. [Maturity-onset diabetes of the young--MODY. Molecular-genetic, pathophysiological and clinical characteristics].
    Hansen T, Urhammer SA, Pedersen OB.
    Ugeskr Laeger; 2002 Apr 08; 164(15):2017-22. PubMed ID: 11984998
    [Abstract] [Full Text] [Related]

  • 35. Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy.
    Gloyn AL.
    Hum Mutat; 2003 Nov 08; 22(5):353-62. PubMed ID: 14517946
    [Abstract] [Full Text] [Related]

  • 36. Restriction fragment length polymorphism of the human insulin gene region among type II diabetic Mexican-Americans and Tunisians.
    Frazier ML, Ferrell RE, Arem R, Chamakhi S, Field JB.
    Res Commun Chem Pathol Pharmacol; 1986 Jun 08; 52(3):371-86. PubMed ID: 3016846
    [Abstract] [Full Text] [Related]

  • 37. Common amino acid substitutions in insulin receptor substrate-4 are not associated with Type II diabetes mellitus or insulin resistance.
    Almind K, Frederiksen SK, Ahlgren MG, Urhammer S, Hansen T, Clausen JO, Pedersen O.
    Diabetologia; 1998 Aug 08; 41(8):969-74. PubMed ID: 9726601
    [Abstract] [Full Text] [Related]

  • 38. Analysis of the insulin gene in noninsulin-dependent diabetes.
    Permutt MA, Rotwein P.
    Am J Med; 1983 Nov 30; 75(5B):1-7. PubMed ID: 6324584
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Hyperinsulinemia is associated with altered insulin receptor mRNA splicing in muscle of the spontaneously obese diabetic rhesus monkey.
    Huang Z, Bodkin NL, Ortmeyer HK, Hansen BC, Shuldiner AR.
    J Clin Invest; 1994 Sep 30; 94(3):1289-96. PubMed ID: 8083370
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.