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Items: 1 to 20 of 89

1.

Candidate genes as potential links between periodontal and cardiovascular diseases.

Kornman KS, Duff GW.

Ann Periodontol. 2001 Dec;6(1):48-57. Review.

PMID:
11887471
2.

Interleukin-1 genotypes and the association between periodontitis and cardiovascular disease.

Kornman KS, Pankow J, Offenbacher S, Beck J, di Giovine F, Duff GW.

J Periodontal Res. 1999 Oct;34(7):353-7.

PMID:
10685360
3.

Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR).

Rozen R.

Thromb Haemost. 1997 Jul;78(1):523-6. Review. No abstract available.

PMID:
9198208
4.

[Role of polymorphic variants of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in the pathogenesis of cardiovascular diseases].

Spiridonova MG, Stepanov VA, Puzyrev VP.

Klin Med (Mosk). 2001;79(2):10-6. Review. Russian. No abstract available.

PMID:
11419077
5.

Interleukin-1 as a genetic marker for periodontitis: review of the literature.

Grigoriadou ME, Koutayas SO, Madianos PN, Strub JR.

Quintessence Int. 2010 Jun;41(6):517-25. Review.

PMID:
20490394
6.

A second common variant in the methylenetetrahydrofolate reductase (MTHFR) gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk.

Lievers KJ, Boers GH, Verhoef P, den Heijer M, Kluijtmans LA, van der Put NM, Trijbels FJ, Blom HJ.

J Mol Med (Berl). 2001 Sep;79(9):522-8.

PMID:
11692165
7.

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

Kluijtmans LA, van den Heuvel LP, Boers GH, Frosst P, Stevens EM, van Oost BA, den Heijer M, Trijbels FJ, Rozen R, Blom HJ.

Am J Hum Genet. 1996 Jan;58(1):35-41.

8.

MTHFR gene polymorphism, homocysteine and cardiovascular disease.

Cortese C, Motti C.

Public Health Nutr. 2001 Apr;4(2B):493-7. Review.

PMID:
11683544
9.

V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit.

Hegele RA, Tully C, Young TK, Connelly PW.

Lancet. 1997 Apr 26;349(9060):1221-2. No abstract available.

PMID:
9130949
10.

Genetic variations in cytokine expression: a risk factor for severity of adult periodontitis.

Kornman KS, di Giovine FS.

Ann Periodontol. 1998 Jul;3(1):327-38. Review.

PMID:
9722717
12.

Genes and gene polymorphisms associated with periodontal disease.

Kinane DF, Hart TC.

Crit Rev Oral Biol Med. 2003;14(6):430-49. Review.

PMID:
14656898
13.

Reduced frequency of the thermolabile methylenetetrahydrofolate reductase genotype in the elderly.

Kluijtmans LA, Whitehead AS.

Atherosclerosis. 1999 Oct;146(2):395-7. No abstract available.

PMID:
10532696
14.

Homocysteine and methylenetetrahydrofolate reductase genotype: association with risk of coronary heart disease and relation to inflammatory, hemostatic, and lipid parameters.

Rothenbacher D, Fischer HG, Hoffmeister A, Hoffmann MM, März W, Bode G, Rosenthal J, Koenig W, Brenner H.

Atherosclerosis. 2002 May;162(1):193-200.

PMID:
11947914
15.

The MTHFR C677T, APOE, and PON55 gene polymorphisms show relevant interactions with cardiovascular risk factors.

Murphy MM, Vilella E, Ceruelo S, Figuera L, Sanchez M, Camps J, Cuco G, Ferré N, Labad A, Tasevska N, Arija V, Joven J, Fernandez-Ballart J.

Clin Chem. 2002 Feb;48(2):372-5. No abstract available.

16.
17.

[Familial predisposition to ischemic cardiopathy: role of homocysteine and genetic polymorphism of methylenetetrahydrofolate reductase].

Potena L, Grigioni F, Mantovani V, Magnani G, Magelli C, Branzi A.

Ital Heart J Suppl. 2001 Jul;2(7):748-53. Review. Italian.

PMID:
11508292
18.

Evidence for an association of the R485K polymorphism in the coagulation factor V gene with severe preeclampsia from screening 35 polymorphisms in 27 candidate genes.

Watanabe H, Hamada H, Yamakawa-Kobayashi K, Yoshikawa H, Arinami T.

Thromb Haemost. 2001 Dec;86(6):1594-5. No abstract available.

PMID:
11776341
19.

Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations.

Isotalo PA, Wells GA, Donnelly JG.

Am J Hum Genet. 2000 Oct;67(4):986-90. Epub 2000 Aug 24.

20.

Methylenetetrahydrofolate reductase (MTHFR). Incidence of the C677T mutation in a Siberian female population.

Belkovets AV, Kurilovich SA, Agarwal DP.

Anthropol Anz. 2001 Mar;59(1):19-25.

PMID:
11360806

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