Novelli G - Search Results

1

Precision Medicine in Non-Communicable Diseases.

Novelli G, Biancolella M, Latini A, Spallone A, Borgiani P, Papaluca M. Novelli G, et al. High Throughput. 2020 Feb 7;9(1):3. doi: 10.3390/ht9010003. High Throughput. 2020. PMID: 32046063 Free PMC article.

2

Role of genetics in prevention of coronary atherosclerosis.

Novelli G, Borgiani P, Giardina E, Mango R, Contino G, Romeo F, Mehta JL. Novelli G, et al. Curr Opin Cardiol. 2003 Sep;18(5):368-71. doi: 10.1097/00001573-200309000-00008. Curr Opin Cardiol. 2003. PMID: 12960469 Review.

3

Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population.

Giardina E, Novelli G, Costanzo A, Nisticò S, Bulli C, Sinibaldi C, Sorgi ML, Chimenti S, Pallone F, Taccari E, Borgiani P. Giardina E, et al. Among authors: novelli g. J Invest Dermatol. 2004 May;122(5):1106-7. doi: 10.1111/j.0022-202X.2004.22524.x. J Invest Dermatol. 2004. PMID: 15140210 Free article.

4

CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease.

Vavassori P, Borgiani P, Biancone L, D'Apice MR, Blanco Gdel V, Vallo L, De Nigris F, Monteleone I, Monteleone G, Pallone F, Novelli G. Vavassori P, et al. Among authors: novelli g. Inflamm Bowel Dis. 2004 Mar;10(2):116-21. doi: 10.1097/00054725-200403000-00009. Inflamm Bowel Dis. 2004. PMID: 15168811

5

Gene expression profiling of fibroblasts from a human progeroid disease (mandibuloacral dysplasia, MAD #248370) through cDNA microarrays.

Amati F, Biancolella M, D'Apice MR, Gambardella S, Mango R, Sbraccia P, D'Adamo M, Margiotti K, Nardone A, Lewis M, Novelli G. Amati F, et al. Among authors: novelli g. Gene Expr. 2004;12(1):39-47. doi: 10.3727/000000004783992189. Gene Expr. 2004. PMID: 15473259 Free PMC article.

6

Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population.

Vallo L, Bonifazi E, Borgiani P, Novelli G, Botta A. Vallo L, et al. Among authors: novelli g. Mol Cell Probes. 2005 Feb;19(1):71-4. doi: 10.1016/j.mcp.2004.09.003. Epub 2004 Nov 12. Mol Cell Probes. 2005. PMID: 15652222

7

Pharmacogenomics in cardiovascular disease: the role of single nucleotide polymorphisms in improving drug therapy.

Mango R, Vecchione L, Raso B, Borgiani P, Brunetti E, Mehta JL, Lauro R, Romeo F, Novelli G. Mango R, et al. Among authors: novelli g. Expert Opin Pharmacother. 2005 Dec;6(15):2565-76. doi: 10.1517/14656566.6.15.2565. Expert Opin Pharmacother. 2005. PMID: 16316297 Review.

8

A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice.

Cipollone D, Amati F, Carsetti R, Placidi S, Biancolella M, D'Amati G, Novelli G, Siracusa G, Marino B. Cipollone D, et al. Among authors: novelli g. Cardiovasc Pathol. 2006 Jul-Aug;15(4):194-202. doi: 10.1016/j.carpath.2006.04.004. Cardiovasc Pathol. 2006. PMID: 16844550

9

Gene expression profile study in CFTR mutated bronchial cell lines.

Gambardella S, Biancolella M, D'Apice MR, Amati F, Sangiuolo F, Farcomeni A, Chillemi G, Bueno S, Desideri A, Novelli G. Gambardella S, et al. Among authors: novelli g. Clin Exp Med. 2006 Dec;6(4):157-65. doi: 10.1007/s10238-006-0116-5. Clin Exp Med. 2006. PMID: 17191107

10

Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development.

Amati F, Biancolella M, Farcomeni A, Giallonardi S, Bueno S, Minella D, Vecchione L, Chillemi G, Desideri A, Novelli G. Amati F, et al. Among authors: novelli g. Gene. 2007 Apr 15;391(1-2):91-102. doi: 10.1016/j.gene.2006.12.026. Epub 2007 Jan 19. Gene. 2007. PMID: 17321697

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