Andreassi MG - Search Results

1

Analysis of miRNAs Targeting 3'UTR of H2AFX Gene: a General in Silico Approach.

Sabina S, Vecoli C, Borghini A, Guarino R, Andreassi MG. Sabina S, et al. Among authors: andreassi mg. Microrna. 2015;4(1):41-9. doi: 10.2174/2211536604666150227232003. Microrna. 2015. PMID: 25738604

2

Adenosine A2(A) receptor gene polymorphism (1976C>T) affects coronary flow reserve response during vasodilator stress testing in patients with non ischemic-dilated cardiomyopathy.

Andreassi MG, Laghi Pasini F, Picano E, Capecchi PL, Pompella G, Foffa I, Borghini A, Sicari R. Andreassi MG, et al. Pharmacogenet Genomics. 2011 Aug;21(8):469-75. doi: 10.1097/FPC.0b013e328347d2c6. Pharmacogenet Genomics. 2011. PMID: 21633321 Clinical Trial.

3

T(-786)→C polymorphism of the endothelial nitric oxide synthase gene is associated with insulin resistance in patients with ischemic or non ischemic cardiomyopathy.

Vecoli C, Andreassi MG, Liga R, Colombo MG, Coceani M, Carpeggiani C, L'Abbate A, Neglia D. Vecoli C, et al. Among authors: andreassi mg. BMC Med Genet. 2012 Oct 2;13:92. doi: 10.1186/1471-2350-13-92. BMC Med Genet. 2012. PMID: 23031426 Free PMC article.

4

Next generation sequencing in cardiovascular diseases.

Faita F, Vecoli C, Foffa I, Andreassi MG. Faita F, et al. Among authors: andreassi mg. World J Cardiol. 2012 Oct 26;4(10):288-95. doi: 10.4330/wjc.v4.i10.288. World J Cardiol. 2012. PMID: 23110245 Free PMC article.

5

Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.

Cresci M, Vecoli C, Foffa I, Pulignani S, Ait-Ali L, Andreassi MG. Cresci M, et al. Among authors: andreassi mg. Pediatr Cardiol. 2013 Apr;34(4):938-41. doi: 10.1007/s00246-012-0578-z. Epub 2012 Nov 15. Pediatr Cardiol. 2013. PMID: 23229290

6

Congenital anomalies among live births in a polluted area. A ten-year retrospective study.

Gianicolo EA, Bruni A, Rosati E, Sabina S, Guarino R, Padolecchia G, Leo C, Vigotti MA, Andreassi MG, Latini G. Gianicolo EA, et al. Among authors: andreassi mg. BMC Pregnancy Childbirth. 2012 Dec 27;12:165. doi: 10.1186/1471-2393-12-165. BMC Pregnancy Childbirth. 2012. PMID: 23270371 Free PMC article.

7

DNA damage and repair in atherosclerosis: current insights and future perspectives.

Cervelli T, Borghini A, Galli A, Andreassi MG. Cervelli T, et al. Among authors: andreassi mg. Int J Mol Sci. 2012 Dec 11;13(12):16929-44. doi: 10.3390/ijms131216929. Int J Mol Sci. 2012. PMID: 23443128 Free PMC article. Review.

8

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: andreassi mg. BMC Med Genet. 2013 Apr 11;14:44. doi: 10.1186/1471-2350-14-44. BMC Med Genet. 2013. PMID: 23578328 Free PMC article.

9

Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.

Sabina S, Pulignani S, Rizzo M, Cresci M, Vecoli C, Foffa I, Ait-Ali L, Pitto L, Andreassi MG. Sabina S, et al. Among authors: andreassi mg. J Mol Cell Cardiol. 2013 Jul;60:84-9. doi: 10.1016/j.yjmcc.2013.04.002. Epub 2013 Apr 11. J Mol Cell Cardiol. 2013. PMID: 23583740 Clinical Trial.

10

Development of a new multiplex quantitative real-time PCR assay for the detection of the mtDNA(4977) deletion in coronary artery disease patients: a link with telomere shortening.

Sabatino L, Botto N, Borghini A, Turchi S, Andreassi MG. Sabatino L, et al. Among authors: andreassi mg. Environ Mol Mutagen. 2013 Jun;54(5):299-307. doi: 10.1002/em.21783. Epub 2013 May 24. Environ Mol Mutagen. 2013. PMID: 23703697

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