Andreassi MG - Search Results

1

Coronary atherosclerosis and somatic mutations: an overview of the contributive factors for oxidative DNA damage.

Andreassi MG. Andreassi MG. Mutat Res. 2003 Jan;543(1):67-86. doi: 10.1016/s1383-5742(02)00089-3. Mutat Res. 2003. PMID: 12510018 Review.

2

Induction of binucleation in human lymphocytes by 14 synthetic isoindolone derivatives related to cytochalasins.

Migliore L, Pistelli L, Papa S, Andreassi MG, Balata T, Benassi S. Migliore L, et al. Among authors: andreassi mg. Mutat Res. 1994 Aug;313(1):89-97. doi: 10.1016/0165-1161(94)90036-1. Mutat Res. 1994. PMID: 7519314

3

Effects of chronic long-term therapy with calcium antagonists on cytogenetic damage in humans.

Andreassi MG, Picano E, Del Ry S, Petrozzi L, Giannessi D, Varga A. Andreassi MG, et al. J Hypertens. 1999 Jun;17(6):843-6. doi: 10.1097/00004872-199917060-00017. J Hypertens. 1999. PMID: 10459883

4

Genetic instability and atherosclerosis: can somatic mutations account for the development of cardiovascular diseases?

Andreassi MG, Botto N, Colombo MG, Biagini A, Clerico A. Andreassi MG, et al. Environ Mol Mutagen. 2000;35(4):265-9. doi: 10.1002/1098-2280(2000)35:4<265::aid-em1>3.0.co;2-m. Environ Mol Mutagen. 2000. PMID: 10861945 Review.

5

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: andreassi mg. Mutat Res. 2001 Jun 27;493(1-2):23-30. doi: 10.1016/s1383-5718(01)00162-0. Mutat Res. 2001. PMID: 11516712

6

Evidence for association of a common variant of the endothelial nitric oxide synthase gene (Glu298-->Asp polymorphism) to the presence, extent, and severity of coronary artery disease.

Colombo MG, Andreassi MG, Paradossi U, Botto N, Manfredi S, Masetti S, Rossi G, Clerico A, Biagini A. Colombo MG, et al. Among authors: andreassi mg. Heart. 2002 Jun;87(6):525-8. doi: 10.1136/heart.87.6.525. Heart. 2002. PMID: 12010932 Free PMC article.

7

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. Among authors: andreassi mg. Environ Mol Mutagen. 2002;40(2):110-5. doi: 10.1002/em.10098. Environ Mol Mutagen. 2002. PMID: 12203403

8

Deoxyribonucleic acid damage in human lymphocytes after percutaneous transluminal coronary angioplasty.

Andreassi MG, Botto N, Rizza A, Colombo MG, Palmieri C, Berti S, Manfredi S, Masetti S, Clerico A, Biagini A. Andreassi MG, et al. J Am Coll Cardiol. 2002 Sep 4;40(5):862-8. doi: 10.1016/s0735-1097(02)02042-9. J Am Coll Cardiol. 2002. PMID: 12225708

9

Elevated levels of oxidative DNA damage in patients with coronary artery disease.

Botto N, Masetti S, Petrozzi L, Vassalle C, Manfredi S, Biagini A, Andreassi MG. Botto N, et al. Among authors: andreassi mg. Coron Artery Dis. 2002 Aug;13(5):269-74. doi: 10.1097/00019501-200208000-00004. Coron Artery Dis. 2002. PMID: 12394651

10

Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease.

Andreassi MG, Botto N, Cocci F, Battaglia D, Antonioli E, Masetti S, Manfredi S, Colombo MG, Biagini A, Clerico A. Andreassi MG, et al. Hum Genet. 2003 Feb;112(2):171-7. doi: 10.1007/s00439-002-0859-3. Epub 2002 Nov 13. Hum Genet. 2003. PMID: 12522558

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