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    Results: 1 to 20 of 110

    1.

    Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies.

    Mesa JL, Loos RJ, Franks PW, Ong KK, Luan J, O'Rahilly S, Wareham NJ, Barroso I.

    Diabetes. 2007 Mar;56(3):884-9.PMID: 17327461 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Variation in the lamin A/C gene: associations with metabolic syndrome.

    Steinle NI, Kazlauskaite R, Imumorin IG, Hsueh WC, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR.

    Arterioscler Thromb Vasc Biol. 2004 Sep;24(9):1708-13. Epub 2004 Jun 17.PMID: 15205219 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects.

    Owen KR, Groves CJ, Hanson RL, Knowler WC, Shuldiner AR, Elbein SC, Mitchell BD, Froguel P, Ng MC, Chan JC, Jia W, Deloukas P, Hitman GA, Walker M, Frayling TM, Hattersley AT, Zeggini E, McCarthy MI.

    Diabetes. 2007 Mar;56(3):879-83.PMID: 17327460 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids.

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

    Diabetologia. 2008 Jan;51(1):76-81. Epub 2007 Nov 10.PMID: 17994215 [PubMed - indexed for MEDLINE]Related articles

    5.

    Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians.

    Weyer C, Wolford JK, Hanson RL, Foley JE, Tataranni PA, Bogardus C, Pratley RE.

    Mol Genet Metab. 2001 Mar;72(3):231-8.PMID: 11243729 [PubMed - indexed for MEDLINE]Related articles

    6.

    Analysis of the lamin A/C gene as a candidate for type II diabetes susceptibility in Pima Indians.

    Wolford JK, Hanson RL, Bogardus C, Prochazka M.

    Diabetologia. 2001 Jun;44(6):779-82.PMID: 11440372 [PubMed - indexed for MEDLINE]Related articles

    7.

    The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.

    Ng MC, Miyake K, So WY, Poon EW, Lam VK, Li JK, Cox NJ, Bell GI, Chan JC.

    Diabetologia. 2005 Oct;48(10):2018-24. Epub 2005 Aug 26.PMID: 16132950 [PubMed - indexed for MEDLINE]Related articles

    8.

    Analysis of genetic variation in Akt2/PKB-beta in severe insulin resistance, lipodystrophy, type 2 diabetes, and related metabolic phenotypes.

    Tan K, Kimber WA, Luan J, Soos MA, Semple RK, Wareham NJ, O'Rahilly S, Barroso I.

    Diabetes. 2007 Mar;56(3):714-9.PMID: 17327441 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7,495 Danish whites.

    Wegner L, Andersen G, Sparsø T, Grarup N, Glümer C, Borch-Johnsen K, Jørgensen T, Hansen T, Pedersen O.

    Diabetes. 2007 Mar;56(3):694-8.PMID: 17327437 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome.

    Decaudain A, Vantyghem MC, Guerci B, Hécart AC, Auclair M, Reznik Y, Narbonne H, Ducluzeau PH, Donadille B, Lebbé C, Béréziat V, Capeau J, Lascols O, Vigouroux C.

    J Clin Endocrinol Metab. 2007 Dec;92(12):4835-44. Epub 2007 Aug 21.PMID: 17711925 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes.

    Liang H, Murase Y, Katuta Y, Asano A, Kobayashi J, Mabuchi H.

    Clin Endocrinol (Oxf). 2005 Sep;63(3):317-22.PMID: 16117820 [PubMed - indexed for MEDLINE]Related articles

    12.

    The role of genetic variation in the lamin a/c gene in the etiology of polycystic ovary syndrome.

    Urbanek M, Nampiaparampil G, D'Souza J, Sefton E, Ackerman C, Legro RS, Dunaif A.

    J Clin Endocrinol Metab. 2009 Jul;94(7):2665-9. Epub 2009 Apr 28.PMID: 19401371 [PubMed - indexed for MEDLINE]Related articles

    13.

    Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophy.

    Vantyghem MC, Vincent-Desplanques D, Defrance-Faivre F, Capeau J, Fermon C, Valat AS, Lascols O, Hecart AC, Pigny P, Delemer B, Vigouroux C, Wemeau JL.

    J Clin Endocrinol Metab. 2008 Jun;93(6):2223-9. Epub 2008 Mar 25.PMID: 18364375 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    The Val81 missense mutation of the melanocortin 3 receptor gene, but not the 1908c/T nucleotide polymorphism in lamin A/C gene, is associated with hyperleptinemia and hyperinsulinemia in obese Greek caucasians.

    Yiannakouris N, Melistas L, Kontogianni M, Heist K, Mantzoros CS.

    J Endocrinol Invest. 2004 Sep;27(8):714-20.PMID: 15636422 [PubMed - indexed for MEDLINE]Related articles

    15.

    A LMNA splicing mutation in two sisters with severe Dunnigan-type familial partial lipodystrophy type 2.

    Morel CF, Thomas MA, Cao H, O'Neil CH, Pickering JG, Foulkes WD, Hegele RA.

    J Clin Endocrinol Metab. 2006 Jul;91(7):2689-95. Epub 2006 Apr 24.PMID: 16636128 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    An LMNA variant is associated with dyslipidemia and insulin resistance in the Japanese.

    Murase Y, Yagi K, Katsuda Y, Asano A, Koizumi J, Mabuchi H.

    Metabolism. 2002 Aug;51(8):1017-21.PMID: 12145775 [PubMed - indexed for MEDLINE]Related articles

    17.

    Lack of association between PKLR rs3020781 and NOS1AP rs7538490 and type 2 diabetes, overweight, obesity and related metabolic phenotypes in a Danish large-scale study: case-control studies and analyses of quantitative traits.

    Andreasen CH, Mogensen MS, Borch-Johnsen K, Sandbaek A, Lauritzen T, Almind K, Hansen L, Jørgensen T, Pedersen O, Hansen T.

    BMC Med Genet. 2008 Dec 26;9:118.PMID: 19111066 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Laminopathies and atherosclerosis.

    Al-Shali KZ, Hegele RA.

    Arterioscler Thromb Vasc Biol. 2004 Sep;24(9):1591-5. Epub 2004 Jun 17. Review.PMID: 15205220 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    AHSG tag single nucleotide polymorphisms associate with type 2 diabetes and dyslipidemia: studies of metabolic traits in 7,683 white Danish subjects.

    Andersen G, Burgdorf KS, Sparsø T, Borch-Johnsen K, Jørgensen T, Hansen T, Pedersen O.

    Diabetes. 2008 May;57(5):1427-32. Epub 2008 Mar 3.PMID: 18316360 [PubMed - indexed for MEDLINE]Related articlesFree article

    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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