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Items: 1 to 20 of 90

1.

Polymorphisms in the PON gene cluster are associated with Alzheimer disease.

Erlich PM, Lunetta KL, Cupples LA, Huyck M, Green RC, Baldwin CT, Farrer LA; MIRAGE Study Group..

Hum Mol Genet. 2006 Jan 1;15(1):77-85. Epub 2005 Nov 30.

PMID:
16319130
2.

Paraoxonase gene cluster variations associated with coronary heart disease in Chinese Han women.

Su SY, Chen JH, Huang JF, Wang XL, Zhao JG, Shen Y, Qiang BQ, Gu DF.

Chin Med J (Engl). 2005 Jul 20;118(14):1167-74.

PMID:
16117861
3.

Genetic association between endothelial nitric oxide synthase and Alzheimer disease.

Akomolafe A, Lunetta KL, Erlich PM, Cupples LA, Baldwin CT, Huyck M, Green RC, Farrer LA; MIRAGE Study Group..

Clin Genet. 2006 Jul;70(1):49-56.

PMID:
16813604
4.
5.

Paraoxonase cluster polymorphisms are associated with sporadic ALS.

Saeed M, Siddique N, Hung WY, Usacheva E, Liu E, Sufit RL, Heller SL, Haines JL, Pericak-Vance M, Siddique T.

Neurology. 2006 Sep 12;67(5):771-6. Epub 2006 Jul 5.

PMID:
16822964
6.

Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease.

Erlich PM, Lunetta KL, Cupples LA, Abraham CR, Green RC, Baldwin CT, Farrer LA.

Neurobiol Aging. 2012 May;33(5):1015.e7-23. doi: 10.1016/j.neurobiolaging.2010.08.003. Epub 2010 Oct 27.

7.
8.

Paraoxonase gene polymorphism and the risk for Alzheimer's disease in the polish population.

Klimkowicz-Mrowiec A, Marona M, Wolkow P, Witkowski A, Maruszak A, Styczynska M, Barcikowska M, Szczudlik A, Slowik A.

Dement Geriatr Cogn Disord. 2011;31(6):417-23. doi: 10.1159/000329571. Epub 2011 Jul 13.

PMID:
21757906
9.

Association study of the paraoxonase 1 gene with the risk of developing Alzheimer's disease.

Chapuis J, Boscher M, Bensemain F, Cottel D, Amouyel P, Lambert JC.

Neurobiol Aging. 2009 Jan;30(1):152-6. Epub 2007 Jul 12.

PMID:
17624629
10.

Mutation screen of the GAD2 gene and association study of alcoholism in three populations.

Lappalainen J, Krupitsky E, Kranzler HR, Luo X, Remizov M, Pchelina S, Taraskina A, Zvartau E, Räsanen P, Makikyro T, Somberg LK, Krystal JH, Stein MB, Gelernter J.

Am J Med Genet B Neuropsychiatr Genet. 2007 Mar 5;144B(2):183-92.

PMID:
17034009
12.

Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease.

Borroni B, Grassi M, Costanzi C, Zanetti M, Archetti S, Franzoni S, Caimi L, Padovani A.

Neurobiol Aging. 2007 Aug;28(8):1231-8. Epub 2006 Jul 11.

PMID:
16837108
13.

Gln192Arg polymorphism in paraoxonase 1 gene is associated with Alzheimer disease in a Chinese Han ethnic population.

He XM, Zhang ZX, Zhang JW, Zhou YT, Tang MN, Wu CB, Hong Z.

Chin Med J (Engl). 2006 Jul 20;119(14):1204-9.

PMID:
16863614
14.

Paraoxonase 1 gene promoter polymorphisms are associated with the extent of stenosis in coronary arteries.

Najafi M, Gohari LH, Firoozrai M.

Thromb Res. 2009;123(3):503-10. doi: 10.1016/j.thromres.2008.03.004. Epub 2008 Apr 22.

PMID:
18433845
15.

Association of polymorphisms in the promoter region of the PNMT gene with essential hypertension in African Americans but not in whites.

Cui J, Zhou X, Chazaro I, DeStefano AL, Manolis AJ, Baldwin CT, Gavras H.

Am J Hypertens. 2003 Oct;16(10):859-63.

PMID:
14553966
16.

Sequence variation of bradykinin receptors B1 and B2 and association with hypertension.

Cui J, Melista E, Chazaro I, Zhang Y, Zhou X, Manolis AJ, Baldwin CT, Destefano AL, Gavras H.

J Hypertens. 2005 Jan;23(1):55-62.

PMID:
15643125
17.

Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene.

Koda Y, Tachida H, Soejima M, Takenaka O, Kimura H.

Ann Hum Genet. 2004 Mar;68(Pt 2):110-9.

PMID:
15008790
18.

Intronic variants in the dopa decarboxylase (DDC) gene are associated with smoking behavior in European-Americans and African-Americans.

Yu Y, Panhuysen C, Kranzler HR, Hesselbrock V, Rounsaville B, Weiss R, Brady K, Farrer LA, Gelernter J.

Hum Mol Genet. 2006 Jul 15;15(14):2192-9. Epub 2006 Jun 1.

PMID:
16740595
19.

Investigation of the estrogen receptor-alpha gene with type 2 diabetes and/or nephropathy in African-American and European-American populations.

Gallagher CJ, Keene KL, Mychaleckyj JC, Langefeld CD, Hirschhorn JN, Henderson BE, Gordon CJ, Freedman BI, Rich SS, Bowden DW, Sale MM.

Diabetes. 2007 Mar;56(3):675-84.

20.

Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population.

Tang WC, Yip SP, Lo KK, Ng PW, Choi PS, Lee SY, Yap MK.

Mol Vis. 2007 Apr 4;13:534-44.

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