Focher F - Search Results

1

Super-telomeres in transformed human fibroblasts.

Chiodi I, Belgiovine C, Zongaro S, Ricotti R, Horard B, Lossani A, Focher F, Gilson E, Giulotto E, Mondello C. Chiodi I, et al. Among authors: focher f. Biochim Biophys Acta. 2013 Aug;1833(8):1885-93. doi: 10.1016/j.bbamcr.2013.03.030. Epub 2013 Apr 6. Biochim Biophys Acta. 2013. PMID: 23570868 Free article.

2

Clostridium difficile DNA polymerase IIIC: basis for activity of antibacterial compounds.

Torti A, Lossani A, Savi L, Focher F, Wright GE, Brown NC, Xu WC. Torti A, et al. Among authors: focher f. Curr Enzym Inhib. 2011 Oct;7(3):147-153. doi: 10.2174/157340811798807597. Curr Enzym Inhib. 2011. PMID: 22844265 Free PMC article.

3

N²-Phenyl-9-(hydroxyalkyl)guanines and related compounds are substrates for Herpes simplex virus thymidine kinases.

Lossani A, Savi L, Manikowski A, Maioli A, Gambino J, Focher F, Spadari S, Wright GE. Lossani A, et al. Among authors: focher f. J Mol Biochem. 2012;1(1):21-25. J Mol Biochem. 2012. PMID: 24734222 Free PMC article.

4

Thymidine kinase and uridine-cytidine kinase from Entamoeba histolytica: cloning, characterization, and search for specific inhibitors.

Lossani A, Torti A, Gatti S, Bruno A, Maserati R, Wright GE, Focher F. Lossani A, et al. Among authors: focher f. Parasitology. 2009 May;136(6):595-602. doi: 10.1017/S0031182009005964. Epub 2009 Apr 16. Parasitology. 2009. PMID: 19368743

5

Site-directed Mutagenesis of Key Residues Unveiled a Novel Allosteric Site on Human Adenosine Kinase for Pyrrolobenzoxa(thia)zepinone Non-Nucleoside Inhibitors.

Savi L, Brindisi M, Alfano G, Butini S, La Pietra V, Novellino E, Marinelli L, Lossani A, Focher F, Cavella C, Campiani G, Gemma S. Savi L, et al. Among authors: focher f. Chem Biol Drug Des. 2016 Jan;87(1):112-20. doi: 10.1111/cbdd.12630. Epub 2015 Sep 18. Chem Biol Drug Des. 2016. PMID: 26242695

6

Enzymes of DNA metabolism in a patient with the Wiedemann-Rautenstrauch progeroid syndrome.

Mazzarello P, Verri A, Mondello C, Colombo S, Maga G, Spadari S, Focher F. Mazzarello P, et al. Among authors: focher f. Ann N Y Acad Sci. 1992 Nov 21;663:440-1. doi: 10.1111/j.1749-6632.1992.tb38694.x. Ann N Y Acad Sci. 1992. PMID: 1482079 No abstract available.

7

Microwave-assisted synthesis and biological evaluation of novel uracil derivatives inhibiting human thymidine phosphorylase.

Corelli F, Botta M, Lossani A, Pasquini S, Spadari S, Focher F. Corelli F, et al. Among authors: focher f. Farmaco. 2004 Dec;59(12):987-92. doi: 10.1016/j.farmac.2004.08.007. Farmaco. 2004. PMID: 15598434

8

Non-nucleoside inhibitors of human adenosine kinase: synthesis, molecular modeling, and biological studies.

Butini S, Gemma S, Brindisi M, Borrelli G, Lossani A, Ponte AM, Torti A, Maga G, Marinelli L, La Pietra V, Fiorini I, Lamponi S, Campiani G, Zisterer DM, Nathwani SM, Sartini S, La Motta C, Da Settimo F, Novellino E, Focher F. Butini S, et al. Among authors: focher f. J Med Chem. 2011 Mar 10;54(5):1401-20. doi: 10.1021/jm101438u. Epub 2011 Feb 14. J Med Chem. 2011. PMID: 21319802

9

Simplified analogues of immucillin-G retain potent human purine nucleoside phosphorylase inhibitory activity.

Semeraro T, Lossani A, Botta M, Ghiron C, Alvarez R, Manetti F, Mugnaini C, Valensin S, Focher F, Corelli F. Semeraro T, et al. Among authors: focher f. J Med Chem. 2006 Oct 5;49(20):6037-45. doi: 10.1021/jm060547+. J Med Chem. 2006. PMID: 17004717

10

Enantioselective binding of second generation pyrrolobenzoxazepinones to the catalytic ternary complex of HIV-1 RT wild-type and L100I and K103N drug resistant mutants.

Butini S, Gemma S, Brindisi M, Borrelli G, Fiorini I, Samuele A, Karytinos A, Facchini M, Lossani A, Zanoli S, Campiani G, Novellino E, Focher F, Maga G. Butini S, et al. Among authors: focher f. Bioorg Med Chem Lett. 2011 Jul 1;21(13):3935-8. doi: 10.1016/j.bmcl.2011.05.020. Epub 2011 May 14. Bioorg Med Chem Lett. 2011. PMID: 21636271

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