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    Results: 1 to 20 of 222

    1.

    Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers.

    Stride A, Shepherd M, Frayling TM, Bulman MP, Ellard S, Hattersley AT.

    Diabetes Care. 2002 Dec;25(12):2287-91.PMID: 12453975 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect.

    Klupa T, Warram JH, Antonellis A, Pezzolesi M, Nam M, Malecki MT, Doria A, Rich SS, Krolewski AS.

    Diabetes Care. 2002 Dec;25(12):2292-301.PMID: 12453976 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Mutations in the genes for hepatocyte nuclear factor (HNF)-1alpha, -4alpha, -1beta, and -3beta; the dimerization cofactor of HNF-1; and insulin promoter factor 1 are not common causes of early-onset type 2 diabetes in Pima Indians.

    Baier LJ, Permana PA, Traurig M, Dobberfuhl A, Wiedrich C, Sutherland J, Thuillez P, Luczy-Bachman G, Hara M, Horikawa Y, Hinokio Y, Hanson RL, Bogardus C.

    Diabetes Care. 2000 Mar;23(3):302-4.PMID: 10868855 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Beta-cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte nuclear factor-1alpha mutation carriers.

    Stride A, Ellard S, Clark P, Shakespeare L, Salzmann M, Shepherd M, Hattersley AT.

    Diabetes Care. 2005 Jul;28(7):1751-6.PMID: 15983330 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuria.

    Bingham C, Ellard S, Nicholls AJ, Pennock CA, Allen J, James AJ, Satchell SC, Salzmann MB, Hattersley AT.

    Diabetes. 2001 Sep;50(9):2047-52.PMID: 11522670 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Identifying hepatic nuclear factor 1alpha mutations in children and young adults with a clinical diagnosis of type 1 diabetes.

    Lambert AP, Ellard S, Allen LI, Gallen IW, Gillespie KM, Bingley PJ, Hattersley AT.

    Diabetes Care. 2003 Feb;26(2):333-7.PMID: 12547858 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations.

    Pearson ER, Velho G, Clark P, Stride A, Shepherd M, Frayling TM, Bulman MP, Ellard S, Froguel P, Hattersley AT.

    Diabetes. 2001 Feb;50 Suppl 1:S101-7.PMID: 11272165 [PubMed - indexed for MEDLINE]Related articles

    8.

    Hepatocyte nuclear factor 1 alpha (HNF-1 alpha) mutations in maturity-onset diabetes of the young.

    Ellard S.

    Hum Mutat. 2000 Nov;16(5):377-85. Review.PMID: 11058894 [PubMed - indexed for MEDLINE]Related articles

    9.

    Identification of a new mutation in the hepatocyte nuclear factor-1alpha gene in a Polish family with early-onset type 2 diabetes mellitus.

    Malecki MT, Klupa T, Frey J, Cyganek K, Galicka-Stankowska D, Wanic K, Sieradzki J.

    Diabetes Nutr Metab. 2001 Oct;14(5):288-91.PMID: 11806470 [PubMed - indexed for MEDLINE]Related articles

    10.

    Genetic modifiers of the age at diagnosis of diabetes (MODY3) in carriers of hepatocyte nuclear factor-1alpha mutations map to chromosomes 5p15, 9q22, and 14q24.

    Kim SH, Ma X, Klupa T, Powers C, Pezzolesi M, Warram JH, Rich SS, Krolewski AS, Doria A.

    Diabetes. 2003 Aug;52(8):2182-6.PMID: 12882939 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY).

    Ellard S, Bulman MP, Frayling TM, Shepherd M, Hattersley AT.

    Hum Mutat. 2000 Sep;16(3):273.PMID: 10980542 [PubMed - indexed for MEDLINE]Related articles

    12.

    Familial early-onset type 2 diabetes in Chinese patients: obesity and genetics have more significant roles than autoimmunity.

    Ng MC, Lee SC, Ko GT, Li JK, So WY, Hashim Y, Barnett AH, Mackay IR, Critchley JA, Cockram CS, Chan JC.

    Diabetes Care. 2001 Apr;24(4):663-71.PMID: 11315828 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes.

    Doria A, Yang Y, Malecki M, Scotti S, Dreyfus J, O'Keeffe C, Orban T, Warram JH, Krolewski AS.

    Diabetes Care. 1999 Feb;22(2):253-61.PMID: 10333942 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics.

    Owen KR, Shepherd M, Stride A, Ellard S, Hattersley AT.

    Diabet Med. 2002 Sep;19(9):758-61.PMID: 12207813 [PubMed - indexed for MEDLINE]Related articles

    15.

    Familial liver adenomatosis associated with hepatocyte nuclear factor 1alpha inactivation.

    Bacq Y, Jacquemin E, Balabaud C, Jeannot E, Scotto B, Branchereau S, Laurent C, Bourlier P, Pariente D, de Muret A, Fabre M, Bioulac-Sage P, Zucman-Rossi J.

    Gastroenterology. 2003 Nov;125(5):1470-5.PMID: 14598263 [PubMed - indexed for MEDLINE]Related articles

    16.

    Mutation P291fsinsC in the transcription factor hepatocyte nuclear factor-1alpha is dominant negative.

    Yamagata K, Yang Q, Yamamoto K, Iwahashi H, Miyagawa J, Okita K, Yoshiuchi I, Miyazaki J, Noguchi T, Nakajima H, Namba M, Hanafusa T, Matsuzawa Y.

    Diabetes. 1998 Aug;47(8):1231-5.PMID: 9703322 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Identification of three new mutations of the HNF-1 alpha gene in Japanese MODY families.

    Ikema T, Shimajiri Y, Komiya I, Tawata M, Sunakawa S, Yogi H, Shimabukuro M, Takasu N.

    Diabetologia. 2002 Dec;45(12):1713-8. Epub 2002 Nov 12.PMID: 12488962 [PubMed - indexed for MEDLINE]Related articles

    18.

    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;44(11):2098-103.PMID: 11719843 [PubMed - indexed for MEDLINE]Related articles

    19.

    Mutation in hepatocyte nuclear factor-1alpha is not a common cause of MODY and early-onset type 2 diabetes in Korea.

    Lee HJ, Ahn CW, Kim SJ, Song YD, Lim SK, Kim KR, Lee HC, Huh KB.

    Acta Diabetol. 2001;38(3):123-7.PMID: 11827432 [PubMed - indexed for MEDLINE]Related articles

    20.

    Regulation of apolipoprotein M gene expression by MODY3 gene hepatocyte nuclear factor-1alpha: haploinsufficiency is associated with reduced serum apolipoprotein M levels.

    Richter S, Shih DQ, Pearson ER, Wolfrum C, Fajans SS, Hattersley AT, Stoffel M.

    Diabetes. 2003 Dec;52(12):2989-95.PMID: 14633861 [PubMed - indexed for MEDLINE]Related articlesFree article

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