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Items: 1 to 20 of 107

1.

Prevalence of MTHFR, Factor V, ACE and APOE gene polymorphisms among Muslims of Manipur, India.

Asghar M, Kabita S, Kalla L, Murry B, Saraswathy KN.

Ann Hum Biol. 2013 Jan;40(1):83-7. doi: 10.3109/03014460.2012.737832. Epub 2012 Oct 31.

PMID:
23110422
2.

Frequency of APOE, MTHFR and ACE polymorphisms in the Zambian population.

Atadzhanov M, Mwaba MH, Mukomena PN, Lakhi S, Mwaba P, Rayaprolu S, Meschia JF, Ross OA.

BMC Res Notes. 2014 Mar 28;7:194. doi: 10.1186/1756-0500-7-194.

3.

MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection.

Jara-Prado A, Alonso ME, Martínez Ruano L, Guerrero Camacho J, Leyva A, López M, Gutierrez-Castrellon P, Arauz A.

Int J Stroke. 2010 Apr;5(2):80-5. doi: 10.1111/j.1747-4949.2010.00412.x.

PMID:
20446941
4.

MTHFR C677T, A1298C and ACE I/D polymorphisms as risk factors for diabetic nephropathy among type 2 diabetic patients.

El-Baz R, Settin A, Ismaeel A, Khaleel AA, Abbas T, Tolba W, Abd Allah W, Sobh MA.

J Renin Angiotensin Aldosterone Syst. 2012 Dec;13(4):472-7. doi: 10.1177/1470320312444651. Epub 2012 May 3.

PMID:
22554825
5.

Evaluation of the interactions of common genetic mutations in stroke subtypes.

Szolnoki Z, Somogyvári F, Kondacs A, Szabó M, Fodor L.

J Neurol. 2002 Oct;249(10):1391-7.

PMID:
12382154
6.

APOE, MTHFR, LDLR and ACE polymorphisms among Angami and Lotha Naga populations of Nagaland, India.

Murry B, Vakha N, Achoubi N, Sachdeva MP, Saraswathy KN.

J Community Health. 2011 Dec;36(6):975-85. doi: 10.1007/s10900-011-9397-z.

PMID:
21461956
7.

Preeclampsia in North Indian women: the contribution of genetic polymorphisms.

Aggarwal S, Dimri N, Tandon I, Agarwal S.

J Obstet Gynaecol Res. 2011 Oct;37(10):1335-41. doi: 10.1111/j.1447-0756.2010.01523.x. Epub 2011 May 12.

PMID:
21564405
8.

Age-dependent prevalence of vascular disease-associated polymorphisms among 2689 volunteer blood donors.

Hessner MJ, Dinauer DM, Kwiatkowski R, Neri B, Raife TJ.

Clin Chem. 2001 Oct;47(10):1879-84.

9.

Migraine and coronary artery disease: an open study on the genetic polymorphism of the 5, 10 methylenetetrahydrofolate (MTHFR) and angiotensin I-converting enzyme (ACE) genes.

Pizza V, Bisogno A, Lamaida E, Agresta A, Bandieramonte G, Volpe A, Galasso R, Galasso L, Caputo M, Tecce MF, Capasso A.

Cent Nerv Syst Agents Med Chem. 2010 Jun 1;10(2):91-6.

PMID:
20518725
10.

Methylenetetrahydrofolate reductase gene polymorphisms are associated with ischemic and hemorrhagic stroke: Dual effect of MTHFR polymorphisms C677T and A1298C.

Sazci A, Ergul E, Tuncer N, Akpinar G, Kara I.

Brain Res Bull. 2006 Dec 11;71(1-3):45-50. Epub 2006 Aug 15.

PMID:
17113927
11.

Role of the ACE ID and MTHFR C677T polymorphisms in genetic susceptibility of migraine in a north Indian population.

Joshi G, Pradhan S, Mittal B.

J Neurol Sci. 2009 Feb 15;277(1-2):133-7. doi: 10.1016/j.jns.2008.11.002. Epub 2008 Dec 9.

PMID:
19081115
12.

Spectrum of MTHFR gene SNPs C677T and A1298C: a study among 23 population groups of India.

Saraswathy KN, Asghar M, Samtani R, Murry B, Mondal PR, Ghosh PK, Sachdeva MP.

Mol Biol Rep. 2012 Apr;39(4):5025-31. doi: 10.1007/s11033-011-1299-8. Epub 2011 Dec 7.

PMID:
22147263
13.

Association between genetic polymorphisms and sites of cervicocerebral artery atherosclerosis.

Chutinet A, Suwanwela NC, Snabboon T, Chaisinanunkul N, Furie KL, Phanthumchinda K.

J Stroke Cerebrovasc Dis. 2012 Jul;21(5):379-85. doi: 10.1016/j.jstrokecerebrovasdis.2010.10.002. Epub 2011 Feb 5.

PMID:
21296594
14.

Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.

Kader HA, Berman WF, Al-Seraihy AS, Ware RE, Ulshen MH, Treem WR.

J Pediatr Gastroenterol Nutr. 2002 Nov;35(5):629-35.

PMID:
12454577
15.

A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.

Almawi WY, Tamim H, Kreidy R, Timson G, Rahal E, Nabulsi M, Finan RR, Irani-Hakime N.

J Thromb Thrombolysis. 2005 Jun;19(3):189-96.

PMID:
16082606
16.

Genetic combination of angiotensin-converting enzyme with methylene tetrahydrofolate reductase polymorphisms and the risk of type 2 diabetes mellitus in Bahrain.

Al-Harbi EM, Farid EM, Gumaa KA, Darwish AH, Alenizi M, Singh J.

J Renin Angiotensin Aldosterone Syst. 2015 Mar;16(1):172-7. doi: 10.1177/1470320313478286. Epub 2013 Feb 27.

PMID:
23447104
17.

Prevalence of thrombotic risk factors among beta-thalassemia patients from Western Iran.

Rahimi Z, Ghaderi M, Nagel RL, Muniz A.

J Thromb Thrombolysis. 2008 Dec;26(3):229-33. Epub 2007 Nov 4.

PMID:
17982733
18.
19.

ACE and MTHFR gene polymorphisms in unexplained recurrent pregnancy loss.

Vettriselvi V, Vijayalakshmi K, Paul SF, Venkatachalam P.

J Obstet Gynaecol Res. 2008 Jun;34(3):301-6. doi: 10.1111/j.1447-0756.2008.00792.x.

PMID:
18588608
20.

Prevalence of MTHFR gene polymorphisms (C677T and A1298C) among Tamilians.

Angeline T, Jeyaraj N, Granito S, Tsongalis GJ.

Exp Mol Pathol. 2004 Oct;77(2):85-8.

PMID:
15351230

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