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Journal Abstract Search

216 related items for PubMed ID: 9267996

  • 1.
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  • 2. Genetic variation in the hepatocyte nuclear factor-1 alpha gene in Danish Caucasians with late-onset NIDDM.
    Urhammer SA, Rasmussen SK, Kaisaki PJ, Oda N, Yamagata K, Møller AM, Fridberg M, Hansen L, Hansen T, Bell GI, Pedersen O.
    Diabetologia; 1997 Apr; 40(4):473-5. PubMed ID: 9112026
    [Abstract] [Full Text] [Related]

  • 3. Variants in the hepatocyte nuclear factor-1alpha and -4alpha genes in Finnish and Chinese subjects with late-onset type 2 diabetes.
    Rissanen J, Wang H, Miettinen R, Kärkkäinen P, Kekäläinen P, Mykkänen L, Kuusisto J, Karhapää P, Niskanen L, Uusitupa M, Laakso M.
    Diabetes Care; 2000 Oct; 23(10):1533-8. PubMed ID: 11023148
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  • 4. Variability of the insulin receptor substrate-1, hepatocyte nuclear factor-1alpha (HNF-1alpha), HNF-4alpha, and HNF-6 genes and size at birth in a population-based sample of young Danish subjects.
    Rasmussen SK, Urhammer SA, Hansen T, Almind K, Møller AM, Borch-Johnsen K, Pedersen O.
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2951-3. PubMed ID: 10946909
    [Abstract] [Full Text] [Related]

  • 5. Mutations in the hepatocyte nuclear factor-4alpha gene in Japanese with non-insulin-dependent diabetes: a nucleotide substitution in the polypyrimidine tract of intron 1b.
    Sakurai K, Seki N, Fujii R, Yagui K, Tokuyama Y, Shimada F, Makino H, Suzuki Y, Hashimoto N, Saito Y, Egashira T, Matsui K, Kanatsuka A.
    Horm Metab Res; 2000 Aug; 32(8):316-20. PubMed ID: 10983627
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  • 7. A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus.
    Hani EH, Suaud L, Boutin P, Chèvre JC, Durand E, Philippi A, Demenais F, Vionnet N, Furuta H, Velho G, Bell GI, Laine B, Froguel P.
    J Clin Invest; 1998 Feb 01; 101(3):521-6. PubMed ID: 9449683
    [Abstract] [Full Text] [Related]

  • 8. No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY.
    Hara M, Wang X, Paz VP, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, Bell GI.
    Diabetologia; 2000 Aug 01; 43(8):1064-9. PubMed ID: 10990086
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  • 10. Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene.
    Lindner T, Gragnoli C, Furuta H, Cockburn BN, Petzold C, Rietzsch H, Weiss U, Schulze J, Bell GI.
    J Clin Invest; 1997 Sep 15; 100(6):1400-5. PubMed ID: 9294105
    [Abstract] [Full Text] [Related]

  • 11. T130I mutation in HNF-4alpha gene is a loss-of-function mutation in hepatocytes and is associated with late-onset Type 2 diabetes mellitus in Japanese subjects.
    Zhu Q, Yamagata K, Miura A, Shihara N, Horikawa Y, Takeda J, Miyagawa J, Matsuzawa Y.
    Diabetologia; 2003 Apr 15; 46(4):567-73. PubMed ID: 12669197
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  • 12.
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  • 13. Triple genetic variation in the HNF-4alpha gene is associated with early-onset type 2 diabetes mellitus in a philippino family.
    Gragnoli C, Menzinger Von Preussenthal G, Habener JF.
    Metabolism; 2004 Aug 15; 53(8):959-63. PubMed ID: 15281001
    [Abstract] [Full Text] [Related]

  • 14. Identification of new mutations in the hepatocyte nuclear factor 4alpha gene among families with early onset Type 2 diabetes mellitus.
    Malecki MT, Yang Y, Antonellis A, Curtis S, Warram JH, Krolewski AS.
    Diabet Med; 1999 Mar 15; 16(3):193-200. PubMed ID: 10227563
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  • 15.
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  • 16. A prevalent amino acid polymorphism at codon 98 in the hepatocyte nuclear factor-1alpha gene is associated with reduced serum C-peptide and insulin responses to an oral glucose challenge.
    Urhammer SA, Fridberg M, Hansen T, Rasmussen SK, Møller AM, Clausen JO, Pedersen O.
    Diabetes; 1997 May 15; 46(5):912-6. PubMed ID: 9133564
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  • 17.
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  • 18. A distant upstream promoter of the HNF-4alpha gene connects the transcription factors involved in maturity-onset diabetes of the young.
    Thomas H, Jaschkowitz K, Bulman M, Frayling TM, Mitchell SM, Roosen S, Lingott-Frieg A, Tack CJ, Ellard S, Ryffel GU, Hattersley AT.
    Hum Mol Genet; 2001 Sep 15; 10(19):2089-97. PubMed ID: 11590126
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  • 20. Mutation screening in 18 Caucasian families suggest the existence of other MODY genes.
    Chèvre JC, Hani EH, Boutin P, Vaxillaire M, Blanché H, Vionnet N, Pardini VC, Timsit J, Larger E, Charpentier G, Beckers D, Maes M, Bellanné-Chantelot C, Velho G, Froguel P.
    Diabetologia; 1998 Sep 15; 41(9):1017-23. PubMed ID: 9754819
    [Abstract] [Full Text] [Related]

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