Manfredi S - Search Results

1

GSTM1, GSTT1 and CYP1A1 detoxification gene polymorphisms and susceptibility to smoking-related coronary artery disease: a case-only study.

Manfredi S, Federici C, Picano E, Botto N, Rizza A, Andreassi MG. Manfredi S, et al. Mutat Res. 2007 Aug 1;621(1-2):106-12. doi: 10.1016/j.mrfmmm.2007.02.014. Epub 2007 Mar 2. Mutat Res. 2007. PMID: 17408703

2

P53 codon 72 polymorphism in coronary artery disease: no evidence for association with increased risk or micronucleus frequency.

Manfredi S, Masetti S, Botto N, Colombo MG, Terrazzi M, Vassalle C, Biagini A, Andreassi MG. Manfredi S, et al. Environ Mol Mutagen. 2002;40(2):110-5. doi: 10.1002/em.10098. Environ Mol Mutagen. 2002. PMID: 12203403

3

Endothelial nitric oxide synthase gene polymorphisms and risk of coronary artery disease.

Colombo MG, Paradossi U, Andreassi MG, Botto N, Manfredi S, Masetti S, Biagini A, Clerico A. Colombo MG, et al. Among authors: manfredi s. Clin Chem. 2003 Mar;49(3):389-95. doi: 10.1373/49.3.389. Clin Chem. 2003. PMID: 12600950 Free article.

4

Interactive effect of the glutathione S-transferase genes and cigarette smoking on occurrence and severity of coronary artery risk.

Masetti S, Botto N, Manfredi S, Colombo MG, Rizza A, Vassalle C, Clerico A, Biagini A, Andreassi MG. Masetti S, et al. Among authors: manfredi s. J Mol Med (Berl). 2003 Aug;81(8):488-94. doi: 10.1007/s00109-003-0448-5. Epub 2003 Jun 17. J Mol Med (Berl). 2003. PMID: 12811412

5

Detection of mtDNA with 4977 bp deletion in blood cells and atherosclerotic lesions of patients with coronary artery disease.

Botto N, Berti S, Manfredi S, Al-Jabri A, Federici C, Clerico A, Ciofini E, Biagini A, Andreassi MG. Botto N, et al. Among authors: manfredi s. Mutat Res. 2005 Feb 15;570(1):81-8. doi: 10.1016/j.mrfmmm.2004.10.003. Mutat Res. 2005. PMID: 15680405

6

Diabetes and chronic nitrate therapy as co-determinants of somatic DNA damage in patients with coronary artery disease.

Andreassi MG, Botto N, Simi S, Casella M, Manfredi S, Lucarelli M, Venneri L, Biagini A, Picano E. Andreassi MG, et al. Among authors: manfredi s. J Mol Med (Berl). 2005 Apr;83(4):279-86. doi: 10.1007/s00109-005-0634-8. Epub 2005 Mar 16. J Mol Med (Berl). 2005. PMID: 15770499

7

Relation of increased chromosomal damage to future adverse cardiac events in patients with known coronary artery disease.

Federici C, Botto N, Manfredi S, Rizza A, Del Fiandra M, Andreassi MG. Federici C, et al. Among authors: manfredi s. Am J Cardiol. 2008 Nov 15;102(10):1296-300. doi: 10.1016/j.amjcard.2008.07.024. Epub 2008 Sep 5. Am J Cardiol. 2008. PMID: 18993144

8

Glutathione S-transferase T1- and M1-null genotypes and coronary artery disease risk in patients with Type 2 diabetes mellitus.

Manfredi S, Calvi D, del Fiandra M, Botto N, Biagini A, Andreassi MG. Manfredi S, et al. Pharmacogenomics. 2009 Jan;10(1):29-34. doi: 10.2217/14622416.10.1.29. Pharmacogenomics. 2009. PMID: 19102712

9

Genetic polymorphisms in XRCC1, OGG1, APE1 and XRCC3 DNA repair genes, ionizing radiation exposure and chromosomal DNA damage in interventional cardiologists.

Andreassi MG, Foffa I, Manfredi S, Botto N, Cioppa A, Picano E. Andreassi MG, et al. Among authors: manfredi s. Mutat Res. 2009 Jun 18;666(1-2):57-63. doi: 10.1016/j.mrfmmm.2009.04.003. Epub 2009 Apr 22. Mutat Res. 2009. PMID: 19393248

10

Evidence for DNA damage in patients with coronary artery disease.

Botto N, Rizza A, Colombo MG, Mazzone AM, Manfredi S, Masetti S, Clerico A, Biagini A, Andreassi MG. Botto N, et al. Among authors: manfredi s. Mutat Res. 2001 Jun 27;493(1-2):23-30. doi: 10.1016/s1383-5718(01)00162-0. Mutat Res. 2001. PMID: 11516712

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