My NCBI | Sign In
RSS Settings
  • Search:

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

    Results: 1 to 20 of 266

    1.

    Cosegregation of MIDD and MODY in a pedigree: functional and clinical consequences.

    Cervin C, Liljeström B, Tuomi T, Heikkinen S, Tapanainen JS, Groop L, Cilio CM.

    Diabetes. 2004 Jul;53(7):1894-9.PMID: 15220216 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway.

    Bjørkhaug L, Sagen JV, Thorsby P, Søvik O, Molven A, Njølstad PR.

    J Clin Endocrinol Metab. 2003 Feb;88(2):920-31.PMID: 12574234 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Characterization of a naturally occurring mutation (L107I) in the HNF1 alpha (MODY3) gene.

    Cervin C, Orho-Melander M, Ridderstråle M, Lehto M, Barg S, Groop L, Cilio CM.

    Diabetologia. 2002 Dec;45(12):1703-8. Epub 2002 Oct 19.PMID: 12488960 [PubMed - indexed for MEDLINE]Related articles

    4.

    Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients.

    Xu JY, Dan QH, Chan V, Wat NM, Tam S, Tiu SC, Lee KF, Siu SC, Tsang MW, Fung LM, Chan KW, Lam KS.

    Eur J Hum Genet. 2005 Apr;13(4):422-7.PMID: 15657605 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    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

    6.

    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

    7.

    Non-penetrance in a MODY 3 family with a mutation in the hepatic nuclear factor 1alpha gene: implications for predictive testing.

    Miedzybrodzka Z, Hattersley AT, Ellard S, Pearson D, de Silva D, Harvey R, Haites N.

    Eur J Hum Genet. 1999 Sep;7(6):729-32.PMID: 10482964 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    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

    9.

    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

    10.

    Half of clinically defined maturity-onset diabetes of the young patients in Denmark do not have mutations in HNF4A, GCK, and TCF1.

    Johansen A, Ek J, Mortensen HB, Pedersen O, Hansen T.

    J Clin Endocrinol Metab. 2005 Aug;90(8):4607-14. Epub 2005 May 31.PMID: 15928245 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families.

    Domínguez-López A, Miliar-García A, Segura-Kato YX, Riba L, Esparza-López R, Ramírez-Jiménez S, Rodríguez-Torres M, Canizales-Quinteros S, Cabrera-Vásquez S, Fragoso-Ontiveros V, Aguilar-Salinas CA, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Bravo-Ríos LE, Tusié-Luna MT.

    JOP. 2005 May 10;6(3):238-45.PMID: 15883474 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    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

    13.

    Diagnosis and management of maturity-onset diabetes of the young.

    Timsit J, Bellanné-Chantelot C, Dubois-Laforgue D, Velho G.

    Treat Endocrinol. 2005;4(1):9-18. Review.PMID: 15649097 [PubMed - indexed for MEDLINE]Related articles

    14.

    Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1 alpha and glucokinase.

    Gragnoli C, Cockburn BN, Chiaramonte F, Gorini A, Marietti G, Marozzi G, Signorini AM.

    Diabetologia. 2001 Oct;44(10):1326-9.PMID: 11692182 [PubMed - indexed for MEDLINE]Related articles

    15.

    Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy.

    Harrison TJ, Boles RG, Johnson DR, LeBlond C, Wong LJ.

    Am J Ophthalmol. 1997 Aug;124(2):217-21.PMID: 9262546 [PubMed - indexed for MEDLINE]Related articles

    16.

    Hepatocyte nuclear factor-1 alpha gene inactivation: cosegregation between liver adenomatosis and diabetes phenotypes in two maturity-onset diabetes of the young (MODY)3 families.

    Reznik Y, Dao T, Coutant R, Chiche L, Jeannot E, Clauin S, Rousselot P, Fabre M, Oberti F, Fatome A, Zucman-Rossi J, Bellanne-Chantelot C.

    J Clin Endocrinol Metab. 2004 Mar;89(3):1476-80.PMID: 15001650 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Etiology of early-onset type 2 diabetes in Indians: islet autoimmunity and mutations in hepatocyte nuclear factor 1alpha and mitochondrial gene.

    Sahu RP, Aggarwal A, Zaidi G, Shah A, Modi K, Kongara S, Aggarwal S, Talwar S, Chu S, Bhatia V, Bhatia E.

    J Clin Endocrinol Metab. 2007 Jul;92(7):2462-7. Epub 2007 Apr 17.PMID: 17440016 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.

    van Essen EH, Roep BO, 't Hart LM, Jansen JJ, Van den Ouweland JM, Lemkes HH, Maassen JA.

    Diabet Med. 2000 Dec;17(12):841-7.PMID: 11168326 [PubMed - indexed for MEDLINE]Related articles

    19.

    Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations.

    Bellanné-Chantelot C, Chauveau D, Gautier JF, Dubois-Laforgue D, Clauin S, Beaufils S, Wilhelm JM, Boitard C, Noël LH, Velho G, Timsit J.

    Ann Intern Med. 2004 Apr 6;140(7):510-7.PMID: 15068978 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Identification and functional characterization of a novel mutation of hepatocyte nuclear factor-1alpha gene in a Korean family with MODY3.

    Kim KA, Kang K, Chi YI, Chang I, Lee MK, Kim KW, Shoelson SE, Lee MS.

    Diabetologia. 2003 May;46(5):721-7. Epub 2003 Apr 24.PMID: 12712243 [PubMed - indexed for MEDLINE]Related articles

    Supplemental Content

    Filter your results:

    Find related data

    Recent activity