Malacrida S - Search Results

1

Association Between ERCC1 rs3212986 and ERCC2/XPD rs1799793 and OS in Patients With Advanced Esophageal Cancer.

Boldrin E, Malacrida S, Rumiato E, Battaglia G, Ruol A, Amadori A, Saggioro D. Boldrin E, et al. Among authors: malacrida s. Front Oncol. 2019 Feb 21;9:85. doi: 10.3389/fonc.2019.00085. eCollection 2019. Front Oncol. 2019. PMID: 30847299 Free PMC article.

2

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

3

Detection of genetic alterations in cfDNA as a possible strategy to monitor the neoplastic progression of Barrett's esophagus.

Rumiato E, Boldrin E, Malacrida S, Realdon S, Fassan M, Morbin T, Battaglia G, Amadori A, Rugge M, Saggioro D. Rumiato E, et al. Among authors: malacrida s. Transl Res. 2017 Dec;190:16-24.e1. doi: 10.1016/j.trsl.2017.09.004. Epub 2017 Oct 6. Transl Res. 2017. PMID: 29066320

4

Identification of host variants associated with overall survival of esophageal cancer patients receiving platinum-based therapy.

Rumiato E, Boldrin E, Malacrida S, Battaglia G, Sileni VC, Ruol A, Amadori A, Saggioro D. Rumiato E, et al. Among authors: malacrida s. Pharmacogenomics. 2020 Apr;21(6):393-402. doi: 10.2217/pgs-2019-0165. Epub 2020 Apr 14. Pharmacogenomics. 2020. PMID: 32285752

5

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

6

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.

7

Editorial: Human Molecular and Physiological Responses to Hypoxia.

Malacrida S, Strapazzon G, Mrakic-Sposta S, Pun M, Cogo A. Malacrida S, et al. Front Physiol. 2022 Apr 29;13:888005. doi: 10.3389/fphys.2022.888005. eCollection 2022. Front Physiol. 2022. PMID: 35574452 Free PMC article. No abstract available.

8

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.

9

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.

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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