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Items: 1 to 20 of 101

1.

Susceptibility to type 1 diabetes is associated with ApoCIII gene haplotypes.

Hokanson JE, Kinney GL, Cheng S, Erlich HA, Kretowski A, Rewers M.

Diabetes. 2006 Mar;55(3):834-8.

2.

Apolipoprotein C-III protein concentrations and gene polymorphisms in Type 1 diabetes: associations with microvascular disease complications in the DCCT/EDIC cohort.

Klein RL, McHenry MB, Lok KH, Hunter SJ, Le NA, Jenkins AJ, Zheng D, Semler A, Page G, Brown WV, Lyons TJ, Garvey WT; DCCT/EDIC Research Group.

J Diabetes Complications. 2005 Jan-Feb;19(1):18-25.

PMID:
15642486
3.

Apolipoprotein C-III protein concentrations and gene polymorphisms in type 1 diabetes: associations with lipoprotein subclasses.

Klein RL, McHenry MB, Lok KH, Hunter SJ, Le NA, Jenkins AJ, Zheng D, Semler AJ, Brown WV, Lyons TJ, Garvey WT; DCCT/EDIC Research Group.

Metabolism. 2004 Oct;53(10):1296-304.

PMID:
15375785
4.

Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children.

Shoulders CC, Grantham TT, North JD, Gaspardone A, Tomai F, de Fazio A, Versaci F, Gioffre PA, Cox NJ.

Hum Genet. 1996 Nov;98(5):557-66.

PMID:
8882875
5.

Identification of a common risk haplotype for diabetic nephropathy at the protein kinase C-beta1 (PRKCB1) gene locus.

Araki S, Ng DP, Krolewski B, Wyrwicz L, Rogus JJ, Canani L, Makita Y, Haneda M, Warram JH, Krolewski AS.

J Am Soc Nephrol. 2003 Aug;14(8):2015-24.

6.

The HLA 8.1 ancestral haplotype is strongly linked to the C allele of -429T>C promoter polymorphism of receptor of the advanced glycation endproduct (RAGE) gene. Haplotype-independent association of the -429C allele with high hemoglobinA1C levels in diabetic patients.

Laki J, Kiszel P, Vatay A, Blaskó B, Kovács M, Körner A, Madácsy L, Blatniczky L, Almássy Z, Szalai C, Rajczy K, Pozsonyi E, Karádi I, Fazakas A, Hosszúfalusi N, Pánczél P, Arason GJ, Wu YL, Zhou B, Yang Y, Yu CY, Füst G.

Mol Immunol. 2007 Jan;44(4):648-55. Epub 2006 Feb 28.

PMID:
16504296
7.

Association of plasma lipids and apolipoproteins with the insulin response element in the apoC-III promoter region in familial combined hyperlipidemia.

Groenendijk M, Cantor RM, Blom NH, Rotter JI, de Bruin TW, Dallinga-Thie GM.

J Lipid Res. 1999 Jun;40(6):1036-44.

8.

Two newly identified SNPs in the APO AI-CIII intergenic region are strongly associated with familial combined hyperlipidaemia.

Groenendijk M, Cantor RM, Funke H, Dallinga-Thie GM.

Eur J Clin Invest. 2001 Oct;31(10):852-9.

PMID:
11737222
9.

Promoter region -318 C/ T and -1661 A/G CTLA-4 single nucleotide polymorphisms and type 1 diabetes in North Indians.

Baniasadi V, Narain N, Goswami R, Das SN.

Tissue Antigens. 2006 May;67(5):383-9.

PMID:
16671945
10.

Association of VEGF and eNOS gene polymorphisms in type 2 diabetic retinopathy.

Suganthalakshmi B, Anand R, Kim R, Mahalakshmi R, Karthikprakash S, Namperumalsamy P, Sundaresan P.

Mol Vis. 2006 Apr 11;12:336-41.

11.
12.

Genetic variation and association analyses of the nuclear respiratory factor 1 (nRF1) gene in Chinese patients with type 2 diabetes.

Liu Y, Niu N, Zhu X, Du T, Wang X, Chen D, Wu X, Gu HF, Liu Y.

Diabetes. 2008 Mar;57(3):777-82. Epub 2007 Dec 10.

13.

[DNA polymorphisms and haplotypes in the apoAI-CIII gene region and coronary heart disease].

Meng X, Zhang G, Li P, Du Y.

Yi Chuan Xue Bao. 1990;17(6):411-7. Chinese.

PMID:
1981133
14.

CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians.

Gragnoli C.

J Cell Physiol. 2008 Nov;217(2):291-5. doi: 10.1002/jcp.21553.

PMID:
18680108
15.

An apolipoprotein CIII marker associated with hypertriglyceridemia in Caucasians also confers increased risk in a west Japanese population.

Zeng Q, Dammerman M, Takada Y, Matsunaga A, Breslow JL, Sasaki J.

Hum Genet. 1995 Apr;95(4):371-5.

PMID:
7705829
16.

Interleukin IL-18 gene promoter polymorphisms in adult patients with type 1 diabetes mellitus and latent autoimmune diabetes in adults.

Novota P, Kolostova K, Pinterova D, Novak J, Treslova L, Andel M, Cerna M.

Immunol Lett. 2005 Jan 31;96(2):247-51.

PMID:
15585330
17.

The variable number of tandem repeats upstream of the insulin gene is a susceptibility locus for latent autoimmune diabetes in adults.

Desai M, Zeggini E, Horton VA, Owen KR, Hattersley AT, Levy JC, Hitman GA, Walker M, Holman RR, McCarthy MI, Clark A.

Diabetes. 2006 Jun;55(6):1890-4.

18.

No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations.

Cinek O, Hradsky O, Ahmedov G, Slavcev A, Kolouskova S, Kulich M, Sumnik Z.

Diabetes Res Clin Pract. 2007 May;76(2):297-303. Epub 2006 Sep 26.

PMID:
17000021
19.

[A related analysis for alpha, beta fibrinogen gene haplotypes and nucleotide polymorphisms associated with the ischemic stroke in Hainan Han population].

Liang L, Sun C, Liao XP, Xiao F, Chen XD, Huang SX, Tang XL, Wen GQ, Long ZG, Wang XY, Liu GX, Cheng S, Cai WW.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):316-9. Chinese.

PMID:
16767673
20.

Association of sterol regulatory element-binding protein-1c gene polymorphism with type 2 diabetes mellitus, insulin resistance and blood lipid levels in Chinese population.

Liu JX, Liu J, Li PQ, Xie XD, Guo Q, Tian LM, Ma XQ, Zhang JP, Liu J, Gao JY.

Diabetes Res Clin Pract. 2008 Oct;82(1):42-7. doi: 10.1016/j.diabres.2008.06.017. Epub 2008 Aug 8.

PMID:
18692268

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