Malacrida S - Search Results

1

Polymorphisms of innate immunity genes influence disease progression in HIV-1-infected children.

Freguja R, Gianesin K, Del Bianco P, Malacrida S, Rampon O, Zanchetta M, Giaquinto C, De Rossi A. Freguja R, et al. Among authors: malacrida s. AIDS. 2012 Mar 27;26(6):765-8. doi: 10.1097/QAD.0b013e3283514350. AIDS. 2012. PMID: 22269973

2

Role of beta-defensin-1 polymorphisms in mother-to-child transmission of HIV-1.

Ricci E, Malacrida S, Zanchetta M, Montagna M, Giaquinto C, De Rossi A. Ricci E, et al. Among authors: malacrida s. J Acquir Immune Defic Syndr. 2009 May 1;51(1):13-9. doi: 10.1097/QAI.0b013e31819df249. J Acquir Immune Defic Syndr. 2009. PMID: 19390326

3

Toll-like receptor 9 polymorphisms influence mother-to-child transmission of human immunodeficiency virus type 1.

Ricci E, Malacrida S, Zanchetta M, Mosconi I, Montagna M, Giaquinto C, De Rossi A. Ricci E, et al. Among authors: malacrida s. J Transl Med. 2010 May 25;8:49. doi: 10.1186/1479-5876-8-49. J Transl Med. 2010. PMID: 20500814 Free PMC article.

4

The role of genetic variants of Stromal cell-Derived Factor 1 in pediatric HIV-1 infection and disease progression.

Gianesin K, Freguja R, Carmona F, Zanchetta M, Del Bianco P, Malacrida S, Montagna M, Rampon O, Giaquinto C, De Rossi A. Gianesin K, et al. Among authors: malacrida s. PLoS One. 2012;7(9):e44460. doi: 10.1371/journal.pone.0044460. Epub 2012 Sep 4. PLoS One. 2012. PMID: 22962615 Free PMC article.

5

Genetic Variants of the TERT Gene, Telomere Length, and Circulating TERT as Prognostic Markers in Rectal Cancer Patients.

Rampazzo E, Cecchin E, Del Bianco P, Menin C, Spolverato G, Giunco S, Lonardi S, Malacrida S, De Paoli A, Toffoli G, Pucciarelli S, De Rossi A. Rampazzo E, et al. Among authors: malacrida s. Cancers (Basel). 2020 Oct 25;12(11):3115. doi: 10.3390/cancers12113115. Cancers (Basel). 2020. PMID: 33113831 Free PMC article.

6

Studies on the Role of Compartmentalized Profiles of Cytokines in the Risk of Hepatocellular Carcinoma.

Fasolato S, Del Bianco P, Malacrida S, Mattiolo A, Gringeri E, Angeli P, Pontisso P, Calabrò ML. Fasolato S, et al. Among authors: malacrida s. Int J Mol Sci. 2023 Aug 30;24(17):13432. doi: 10.3390/ijms241713432. Int J Mol Sci. 2023. PMID: 37686245 Free PMC article.

7

Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy.

Busolin G, Malacrida S, Bisulli F, Striano P, Di Bonaventura C, Egeo G, Pasini E, Cianci V, Ferlazzo E, Bianchi A, Coppola G, Elia M, Mecarelli O, Gobbi G, Casellato S, Marchini M, Binelli S, Freri E, Granata T, Posar A, Parmeggiani A, Vigliano P, Boniver C, Aguglia U, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Busolin G, et al. Among authors: malacrida s. Epilepsy Res. 2011 Mar;94(1-2):110-6. doi: 10.1016/j.eplepsyres.2011.01.010. Epub 2011 Feb 18. Epilepsy Res. 2011. PMID: 21333500

8

A germline predictive signature of response to platinum chemotherapy in esophageal cancer.

Rumiato E, Boldrin E, Malacrida S, Battaglia G, Bocus P, Castoro C, Cagol M, Chiarion-Sileni V, Ruol A, Amadori A, Saggioro D. Rumiato E, et al. Among authors: malacrida s. Transl Res. 2016 May;171:29-37.e1. doi: 10.1016/j.trsl.2015.12.011. Epub 2015 Dec 22. Transl Res. 2016. PMID: 26772957

9

BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from Northeast Italy.

Malacrida S, Agata S, Callegaro M, Casella C, Barana D, Scaini MC, Manoukian S, Oliani C, Radice P, Barile M, Menin C, D'Andrea E, Montagna M. Malacrida S, et al. J Clin Oncol. 2008 Jan 1;26(1):26-31. doi: 10.1200/JCO.2007.13.2118. J Clin Oncol. 2008. PMID: 18165637

10

Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation.

Scaini MC, Rossi E, de Siqueira Torres PL, Zullato D, Callegaro M, Casella C, Quaggio M, Agata S, Malacrida S, Chiarion-Sileni V, Vecchiato A, Alaibac M, Montagna M, Mann GJ, Menin C, D'Andrea E. Scaini MC, et al. Among authors: malacrida s. Mutat Res. 2009 Dec 1;671(1-2):26-32. doi: 10.1016/j.mrfmmm.2009.08.007. Epub 2009 Aug 25. Mutat Res. 2009. PMID: 19712690

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