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Items: 1 to 20 of 96

1.

Association of reduced folate carrier-1 (RFC-1) polymorphisms with ischemic stroke and silent brain infarction.

Cho Y, Kim JO, Lee JH, Park HM, Jeon YJ, Oh SH, Bae J, Park YS, Kim OJ, Kim NK.

PLoS One. 2015 Feb 6;10(2):e0115295. doi: 10.1371/journal.pone.0115295. eCollection 2015.

2.

Solute Carrier Family 19, member 1 (SLC19A1) polymorphisms (-43T>C, 80G>A, and 696C>T), and haplotypes in idiopathic recurrent spontaneous abortion in a Korean population.

Rah H, Choi YS, Jeon YJ, Choi Y, Cha SH, Choi DH, Ko JJ, Shim SH, Kim NK.

Reprod Sci. 2012 May;19(5):513-9. doi: 10.1177/1933719111426604. Epub 2012 Feb 16.

PMID:
22344739
3.

Association of the miR-146a, miR-149, miR-196a2, and miR-499 polymorphisms with ischemic stroke and silent brain infarction risk.

Jeon YJ, Kim OJ, Kim SY, Oh SH, Oh D, Kim OJ, Shin BS, Kim NK.

Arterioscler Thromb Vasc Biol. 2013 Feb;33(2):420-30. doi: 10.1161/ATVBAHA.112.300251. Epub 2012 Nov 29.

PMID:
23202363
4.

Association between VEGF polymorphisms and homocysteine levels in patients with ischemic stroke and silent brain infarction.

Kim OJ, Hong SH, Oh SH, Kim TG, Min KT, Oh D, Kim NK.

Stroke. 2011 Sep;42(9):2393-402. doi: 10.1161/STROKEAHA.110.607739. Epub 2011 Jul 7.

PMID:
21737794
5.

Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.

Białecka M, Kurzawski M, Roszmann A, Robowski P, Sitek EJ, Honczarenko K, Gorzkowska A, Budrewicz S, Mak M, Jarosz M, Gołąb-Janowska M, Koziorowska-Gawron E, Droździk M, Sławek J.

Pharmacogenet Genomics. 2012 Oct;22(10):716-24. doi: 10.1097/FPC.0b013e32835693f7.

PMID:
22890010
6.

Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population.

Han IB, Kim OJ, Ahn JY, Oh D, Hong SP, Huh R, Chung SS, Kim NK.

Yonsei Med J. 2010 Mar;51(2):253-60. doi: 10.3349/ymj.2010.51.2.253. Epub 2010 Feb 12.

7.

Association of MTHFR, SLC19A1 Genetic Polymorphism, Serum Folate, Vitamin B12 and Hcy Status with Cognitive Functions in Chinese Adults.

Cai C, Xiao R, Van Halm-Lutterodt N, Zhen J, Huang X, Xu Y, Chen S, Yuan L.

Nutrients. 2016 Oct 24;8(10). pii: E665.

8.

Association between tumor necrosis factor-alpha (-308G→A and -238G→A) polymorphisms and homocysteine levels in patients with ischemic strokes and silent brain infarctions.

Kim OJ, Lee JH, Choi JK, Oh SH, Hong SH, Oh D, Kim NK.

Cerebrovasc Dis. 2010;30(5):483-90. doi: 10.1159/000319023. Epub 2010 Aug 25.

PMID:
20798494
9.

Reduced folate carrier polymorphism (80A-->G) and neural tube defects.

De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V.

Eur J Hum Genet. 2003 Mar;11(3):245-52.

10.

ACE I/D polymorphism in Korean patients with ischemic stroke and silent brain infarction.

Hong SH, Park HM, Ahn JY, Kim OJ, Hwang TS, Oh D, Kim NK.

Acta Neurol Scand. 2008 Apr;117(4):244-9. Epub 2007 Oct 8.

PMID:
17922891
11.

Folate, vitamin B12 and Homocysteine status in the post-folic acid fortification era in different subgroups of the Brazilian population attended to at a public health care center.

Barnabé A, Aléssio AC, Bittar LF, de Moraes Mazetto B, Bicudo AM, de Paula EV, Höehr NF, Annichino-Bizzacchi JM.

Nutr J. 2015 Feb 19;14:19. doi: 10.1186/s12937-015-0006-3.

12.

Reduced folate carrier 80A-->G polymorphism, plasma folate, and risk of placental abruption.

Ananth CV, Peltier MR, Moore DF, Kinzler WL, Leclerc D, Rozen RR; New Jersey-Placental Abruption Study Investigators.

Hum Genet. 2008 Sep;124(2):137-45. doi: 10.1007/s00439-008-0531-7. Epub 2008 Jul 16.

13.

A pilot study evaluating the contribution of SLC19A1 (RFC-1) 80G>a polymorphism to Alzheimer's disease in Italian Caucasians.

Coppedè F, Tannorella P, Tognoni G, Bagnoli S, Bongioanni P, Nacmias B, Siciliano G, Sorbi S, Bonuccelli U, Migliore L.

Biomed Res Int. 2014;2014:608104. doi: 10.1155/2014/608104. Epub 2014 Jun 5.

14.

C677t polymorphism of MTHFR and G80A polymorphism of RFC genes and their relation with homocysteine levels in obese Tunisian children.

Gara S, Ochi H, Chango A, Najjar L, Feki M, B'chir F, Kaabachi N, Ben Becher S, Boukthir S, Abdennebi M.

Tunis Med. 2011 Jun;89(6):565-8.

15.

The effect of RFC G80A polymorphism in Cretan children with acute lymphoblastic leukemia and its interaction with MTHFR C677T and A1298C polymorphisms.

Karathanasis NV, Stiakaki E, Goulielmos GΝ, Kalmanti M.

Int J Lab Hematol. 2014 Aug;36(4):425-30. doi: 10.1111/ijlh.12160. Epub 2013 Nov 16.

PMID:
24237708
16.

The reduced folate carrier (RFC-1) 80A>G polymorphism and maternal risk of having a child with Down syndrome: a meta-analysis.

Coppedè F, Lorenzoni V, Migliore L.

Nutrients. 2013 Jul 5;5(7):2551-63. doi: 10.3390/nu5072551.

17.

Association between common genetic variants of α2A-, α2B- and α2C-adrenoceptors and the risk of silent brain infarction.

Kim JO, Jeon YJ, Kim OJ, Oh SH, Kim HS, Shin BS, Oh D, Kim EJ, Cho YK, Kim NK.

Mol Med Rep. 2014 Jun;9(6):2459-66. doi: 10.3892/mmr.2014.2072. Epub 2014 Mar 27.

PMID:
24676565
18.

Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V.

Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7.

PMID:
11813127
19.

Clinical Relevance of MTHFR, eNOS, ACE, and ApoE Gene Polymorphisms and Serum Vitamin Profile among Malay Patients with Ischemic Stroke.

Wei LK, Au A, Menon S, Gan SH, Griffiths LR.

J Stroke Cerebrovasc Dis. 2015 Sep;24(9):2017-25. doi: 10.1016/j.jstrokecerebrovasdis.2015.04.011. Epub 2015 Jul 15.

PMID:
26187788
20.

An Association Study of the SLC19A1 Gene Polymorphisms/Haplotypes with Idiopathic Recurrent Pregnancy Loss in an Iranian Population.

Mohtaram S, Sheikhha MH, Honarvar N, Sazegari A, Maraghechi N, Feizollahi Z, Ghasemi N.

Genet Test Mol Biomarkers. 2016 May;20(5):235-40. doi: 10.1089/gtmb.2015.0230. Epub 2016 Mar 9.

PMID:
26959650

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