Botto N - Search Results

1

Sequencing of NOTCH1, GATA5, TGFBR1 and TGFBR2 genes in familial cases of bicuspid aortic valve.

Foffa I, Ait Alì L, Panesi P, Mariani M, Festa P, Botto N, Vecoli C, Andreassi MG. Foffa I, et al. Among authors: botto n. BMC Med Genet. 2013 Apr 11;14:44. doi: 10.1186/1471-2350-14-44. BMC Med Genet. 2013. PMID: 23578328 Free PMC article.

2

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. Among authors: botto n. 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.

3

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

4

Chronic long-term nitrate therapy: possible cytogenetic effect in humans?

Andreassi MG, Picano E, Del Ry S, Botto N, Colombo MG, Giannessi D, Lubrano V, Vassalle C, Biagini A. Andreassi MG, et al. Among authors: botto n. Mutagenesis. 2001 Nov;16(6):517-21. doi: 10.1093/mutage/16.6.517. Mutagenesis. 2001. PMID: 11682643

5

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: botto n. Heart. 2002 Jun;87(6):525-8. doi: 10.1136/heart.87.6.525. Heart. 2002. PMID: 12010932 Free PMC article.

6

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: botto n. Environ Mol Mutagen. 2002;40(2):110-5. doi: 10.1002/em.10098. Environ Mol Mutagen. 2002. PMID: 12203403

7

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. Among authors: botto n. 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 Free article.

8

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. Coron Artery Dis. 2002 Aug;13(5):269-74. doi: 10.1097/00019501-200208000-00004. Coron Artery Dis. 2002. PMID: 12394651

9

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. Among authors: botto n. Hum Genet. 2003 Feb;112(2):171-7. doi: 10.1007/s00439-002-0859-3. Epub 2002 Nov 13. Hum Genet. 2003. PMID: 12522558

10

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: botto n. Clin Chem. 2003 Mar;49(3):389-95. doi: 10.1373/49.3.389. Clin Chem. 2003. PMID: 12600950 Free article.

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