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    Results: 1 to 20 of 557

    1.

    Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach.

    Gloyn AL, Mackay DJ, Weedon MN, McCarthy MI, Walker M, Hitman G, Knight BA, Owen KR, Hattersley AT, Frayling TM.

    Diabetes. 2006 Aug;55(8):2272-6.PMID: 16873690 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitus.

    Mackay DJ, Coupe AM, Shield JP, Storr JN, Temple IK, Robinson DO.

    Hum Genet. 2002 Feb;110(2):139-44. Epub 2002 Jan 24.PMID: 11935319 [PubMed - indexed for MEDLINE]Related articles

    3.

    The cell cycle control gene ZAC/PLAGL1 is imprinted--a strong candidate gene for transient neonatal diabetes.

    Kamiya M, Judson H, Okazaki Y, Kusakabe M, Muramatsu M, Takada S, Takagi N, Arima T, Wake N, Kamimura K, Satomura K, Hermann R, Bonthron DT, Hayashizaki Y.

    Hum Mol Genet. 2000 Feb 12;9(3):453-60.PMID: 10655556 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus.

    Veal CD, Capon F, Allen MH, Heath EK, Evans JC, Jones A, Patel S, Burden D, Tillman D, Barker JN, Trembath RC.

    Am J Hum Genet. 2002 Sep;71(3):554-64. Epub 2002 Jul 29.PMID: 12148091 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Transient neonatal diabetes, a disorder of imprinting.

    Temple IK, Shield JP.

    J Med Genet. 2002 Dec;39(12):872-5. Review.PMID: 12471198 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitus.

    Varrault A, Bilanges B, Mackay DJ, Basyuk E, Ahr B, Fernandez C, Robinson DO, Bockaert J, Journot L.

    J Biol Chem. 2001 Jun 1;276(22):18653-6. Epub 2001 Apr 10.PMID: 11297535 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

    Silander K, Mohlke KL, Scott LJ, Peck EC, Hollstein P, Skol AD, Jackson AU, Deloukas P, Hunt S, Stavrides G, Chines PS, Erdos MR, Narisu N, Conneely KN, Li C, Fingerlin TE, Dhanjal SK, Valle TT, Bergman RN, Tuomilehto J, Watanabe RM, Boehnke M, Collins FS.

    Diabetes. 2004 Apr;53(4):1141-9.PMID: 15047633 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23.

    Temple IK, Gardner RJ, Robinson DO, Kibirige MS, Ferguson AW, Baum JD, Barber JC, James RS, Shield JP.

    Hum Mol Genet. 1996 Aug;5(8):1117-21.PMID: 8842729 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes.

    Winckler W, Weedon MN, Graham RR, McCarroll SA, Purcell S, Almgren P, Tuomi T, Gaudet D, Boström KB, Walker M, Hitman G, Hattersley AT, McCarthy MI, Ardlie KG, Hirschhorn JN, Daly MJ, Frayling TM, Groop L, Altshuler D.

    Diabetes. 2007 Mar;56(3):685-93.PMID: 17327436 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

    Love-Gregory LD, Wasson J, Ma J, Jin CH, Glaser B, Suarez BK, Permutt MA.

    Diabetes. 2004 Apr;53(4):1134-40.PMID: 15047632 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    A large-scale association analysis of common variation of the HNF1alpha gene with type 2 diabetes in the U.K. Caucasian population.

    Weedon MN, Owen KR, Shields B, Hitman G, Walker M, McCarthy MI, Hattersley AT, Frayling TM.

    Diabetes. 2005 Aug;54(8):2487-91.PMID: 16046319 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Bisulphite sequencing of the transient neonatal diabetes mellitus DMR facilitates a novel diagnostic test but reveals no methylation anomalies in patients of unknown aetiology.

    Mackay DJ, Temple IK, Shield JP, Robinson DO.

    Hum Genet. 2005 Mar;116(4):255-61. Epub 2005 Jan 6.PMID: 15635480 [PubMed - indexed for MEDLINE]Related articles

    13.

    A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus.

    Arima T, Drewell RA, Arney KL, Inoue J, Makita Y, Hata A, Oshimura M, Wake N, Surani MA.

    Hum Mol Genet. 2001 Jul 1;10(14):1475-83.PMID: 11448939 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.

    Arima T, Kamikihara T, Hayashida T, Kato K, Inoue T, Shirayoshi Y, Oshimura M, Soejima H, Mukai T, Wake N.

    Nucleic Acids Res. 2005 May 11;33(8):2650-60. Print 2005.PMID: 15888726 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes.

    Winckler W, Burtt NP, Holmkvist J, Cervin C, de Bakker PI, Sun M, Almgren P, Tuomi T, Gaudet D, Hudson TJ, Ardlie KG, Daly MJ, Hirschhorn JN, Altshuler D, Groop L.

    Diabetes. 2005 Aug;54(8):2336-42.PMID: 16046299 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Functional variation in VEGF is not associated with type 2 diabetes in a United Kingdom Caucasian population.

    Freathy RM, Weedon MN, Shields B, Hitman GA, Walker M, McCarthy MI, Hattersley AT, Frayling TM.

    JOP. 2006 May 9;7(3):295-302.PMID: 16685110 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Study of the genetic variability of ZAC1 (PLAGL1) in French population-based samples.

    Goumidi L, Spengler D, Cottel D, Wagner A, Ducimetière P, Ruidavets JB, Legry V, Arveiler D, Bingham A, Ferrières J, Amouyel P, Meirhaeghe A.

    J Hypertens. 2009 Feb;27(2):314-21.PMID: 19155788 [PubMed - indexed for MEDLINE]Related articles

    18.

    Calsquestrin 1 (CASQ1) gene polymorphisms under chromosome 1q21 linkage peak are associated with type 2 diabetes in Northern European Caucasians.

    Das SK, Chu W, Zhang Z, Hasstedt SJ, Elbein SC.

    Diabetes. 2004 Dec;53(12):3300-6.PMID: 15561963 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population.

    Horikoshi M, Hara K, Ito C, Shojima N, Nagai R, Ueki K, Froguel P, Kadowaki T.

    Diabetologia. 2007 Dec;50(12):2461-6. Epub 2007 Oct 10.PMID: 17928989 [PubMed - indexed for MEDLINE]Related articles

    20.

    Evaluating the association of common PBX1 variants with type 2 diabetes.

    Duesing K, Charpentier G, Marre M, Tichet J, Hercberg S, Balkau B, Froguel P, Gibson F.

    BMC Med Genet. 2008 Feb 29;9:14.PMID: 18312624 [PubMed - indexed for MEDLINE]Related articlesFree article

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