Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 151

1.

Association study of two steroid biosynthesis genes (COMT and CYP17) with Alzheimer's disease in the Italian population.

Corbo RM, Gambina G, Broggio E, Scarabino D, Scacchi R.

J Neurol Sci. 2014 Sep 15;344(1-2):149-53. doi: 10.1016/j.jns.2014.06.045. Epub 2014 Jun 29.

PMID:
25012481
2.

Variants in CYP17 and CYP19 cytochrome P450 genes are associated with onset of Alzheimer's disease in women with down syndrome.

Chace C, Pang D, Weng C, Temkin A, Lax S, Silverman W, Zigman W, Ferin M, Lee JH, Tycko B, Schupf N.

J Alzheimers Dis. 2012;28(3):601-12. doi: 10.3233/JAD-2011-110860.

3.

Two single nucleotide polymorphisms in the CYP17 and COMT Genes--relation to bone mass and longitudinal bone changes in postmenopausal women with or without hormone replacement therapy. The Danish Osteoporosis Prevention Study.

Tofteng CL, Abrahamsen B, Jensen JE, Petersen S, Teilmann J, Kindmark A, Vestergaard P, Gram J, Langdahl BL, Mosekilde L.

Calcif Tissue Int. 2004 Aug;75(2):123-32. Epub 2004 Apr 29.

PMID:
15129369
4.

Estrogen-metabolizing gene COMT polymorphism synergistic APOE epsilon4 allele increases the risk of Alzheimer disease.

Wang PN, Liu HC, Liu TY, Chu A, Hong CJ, Lin KN, Chi CW.

Dement Geriatr Cogn Disord. 2005;19(2-3):120-5. Epub 2004 Dec 9.

5.

Association between the catechol-O-methyltransferase polymorphism Val158Met and Alzheimer's disease in a Japanese population.

Shibata N, Nagata T, Tagai K, Shinagawa S, Ohnuma T, Kawai E, Kasanuki K, Shimazaki H, Toda A, Tagata Y, Nakada T, Nakayama K, Yamada H, Arai H.

Int J Geriatr Psychiatry. 2015 Sep;30(9):927-33. doi: 10.1002/gps.4237. Epub 2014 Dec 9.

PMID:
25491588
6.

Influence of COMT Val158Met polymorphism on Alzheimer's disease and mild cognitive impairment in Italian patients.

Lanni C, Garbin G, Lisa A, Biundo F, Ranzenigo A, Sinforiani E, Cuzzoni G, Govoni S, Ranzani GN, Racchi M.

J Alzheimers Dis. 2012;32(4):919-26. doi: 10.3233/JAD-2012-120358.

PMID:
22890094
7.

Lack of association between COMT Val158Met polymorphism and late-onset Alzheimer's disease in Han Chinese.

Zhou J, Li XM, Jiang T, Liu Y, Chi S, Yu JT, Tan L.

Neurosci Lett. 2013 Oct 25;554:162-6. doi: 10.1016/j.neulet.2013.09.006. Epub 2013 Sep 11.

PMID:
24035893
8.

The COMT Val158 Met polymorphism as an associated risk factor for Alzheimer disease and mild cognitive impairment in APOE 4 carriers.

Martínez MF, Martín XE, Alcelay LG, Flores JC, Valiente JM, Juanbeltz BI, Beldarraín MA, López JM, Gonzalez-Fernández MC, Salazar AM, Gandarias RB, Borda SI, Marqués NO, Amillano MB, Zabaleta MC, de Pancorbo MM.

BMC Neurosci. 2009 Sep 30;10:125. doi: 10.1186/1471-2202-10-125.

9.
10.

CYP17, catechol-o-methyltransferase, and glutathione transferase M1 genetic polymorphisms, lifestyle factors, and breast cancer risk in women on Prince Edward Island.

Cribb AE, Joy Knight M, Guernsey J, Dryer D, Hender K, Shawwa A, Tesch M, Saleh TM.

Breast J. 2011 Jan-Feb;17(1):24-31. doi: 10.1111/j.1524-4741.2010.01025.x. Epub 2010 Dec 6.

PMID:
21129090
11.

CYP17 and COMT gene polymorphisms can influence bone directly, or indirectly through their effects on endogenous sex steroids, in postmenopausal Japanese women.

Gorai I, Inada M, Morinaga H, Uchiyama Y, Yamauchi H, Hirahara F, Chaki O.

Bone. 2007 Jan;40(1):28-36. Epub 2006 Sep 12.

PMID:
16971197
12.

Polymorphisms in CYP17, COMT, and ESR1 genes in women after menopause and association with bone mineral density.

Gonçalves CG, Almeida BC, Camargo-Kosugi CM, Costa AM, Silva ID, Haidar MA.

Genet Mol Res. 2015 Dec 2;14(4):15802-10. doi: 10.4238/2015.December.1.32.

13.

Polymorphisms of the neurotrophic factor-3 (NTF-3) in Alzheimer's disease: rs6332 associated with onset time and rs6489630 T allele exhibited a protective role.

Liu M, Huo YR, Wang J, Liu S, Liu S, Wang C, Wang J, Ji Y.

J Neurogenet. 2015;29(4):183-7. doi: 10.3109/01677063.2015.1099651.

PMID:
26814132
14.

Catechol-O-methyltransferase genetic variant associated with the risk of Alzheimer's disease in a Brazilian population.

Pereira PA, Romano-Silva MA, Bicalho MA, de Moraes EN, Malloy-Diniz L, Pimenta GJ, Mello MP, Bozzi IC, de Marco LA, Nicolato R, Miranda DM.

Dement Geriatr Cogn Disord. 2012;34(2):90-5. Epub 2012 Aug 27.

PMID:
22922787
15.

Cytochrome P450 17A1 and catechol O-methyltransferase polymorphisms and age at Lynch syndrome colon cancer onset in Newfoundland.

Campbell PT, Edwards L, McLaughlin JR, Green J, Younghusband HB, Woods MO.

Clin Cancer Res. 2007 Jul 1;13(13):3783-8.

16.

Genetic variation in the choline O-acetyltransferase gene in depression and Alzheimer's disease: the VITA and Milano studies.

Grünblatt E, Reif A, Jungwirth S, Galimberti D, Weber H, Scarpini E, Sauer C, Wichart I, Rainer MK, Huber K, Danielczyk W, Tragl KH, Deckert J, Fischer P, Riederer P.

J Psychiatr Res. 2011 Sep;45(9):1250-6. doi: 10.1016/j.jpsychires.2011.03.017. Epub 2011 Apr 19.

PMID:
21507424
17.

Genetic variation of CYP19 (aromatase) gene influences age at onset of Alzheimer's disease in women.

Corbo RM, Gambina G, Ulizzi L, Moretto G, Scacchi R.

Dement Geriatr Cogn Disord. 2009;27(6):513-8. doi: 10.1159/000221832. Epub 2009 May 29.

PMID:
19478482
18.

Association between CYP17A1 rs3824755 and rs743572 gene polymorphisms and Alzheimer's disease in the Chinese Han population.

Xie L, Yan H, Shi L, Kong Y, Huang M, Li J, Li J, Zheng J, Zhao Y, Zhao S.

Neurosci Lett. 2016 Apr 8;618:77-82. doi: 10.1016/j.neulet.2016.02.053. Epub 2016 Mar 3.

PMID:
26940238
19.

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
20.

Genetic Basis of the Relationship Between Reproduction and Longevity: A Study on Common Variants of Three Genes in Steroid Hormone Metabolism--CYP17, HSD17B1, and COMT.

Scarabino D, Scacchi R, Pinto A, Corbo RM.

Rejuvenation Res. 2015 Oct;18(5):464-72. doi: 10.1089/rej.2015.1665. Epub 2015 Sep 29.

PMID:
25936248

Supplemental Content

Support Center