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Splicing program of human MENA produces a previously undescribed isoform associated with invasive, mesenchymal-like breast tumors.
Proc Natl Acad Sci U S A. 2012 Nov 20;109(47):19280-5. doi: 10.1073/pnas.1214394109. Epub 2012 Nov 5.
Proc Natl Acad Sci U S A. 2012.
PMID: 23129656
Free PMC article.
hMENA isoforms impact NSCLC patient outcome through fibronectin/β1 integrin axis.
Di Modugno F, Spada S, Palermo B, Visca P, Iapicca P, Di Carlo A, Antoniani B, Sperduti I, Di Benedetto A, Terrenato I, Mottolese M, Gandolfi F, Facciolo F, Chen EI, Schwartz MA, Santoni A, Bissell MJ, Nisticò P.
Di Modugno F, et al. Among authors: iapicca p.
Oncogene. 2018 Oct;37(42):5605-5617. doi: 10.1038/s41388-018-0364-3. Epub 2018 Jun 15.
Oncogene. 2018.
PMID: 29907768
Free PMC article.
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Prognostic impact of alternative splicing-derived hMENA isoforms in resected, node-negative, non-small-cell lung cancer.
Bria E, Di Modugno F, Sperduti I, Iapicca P, Visca P, Alessandrini G, Antoniani B, Pilotto S, Ludovini V, Vannucci J, Bellezza G, Sidoni A, Tortora G, Radisky DC, Crinò L, Cognetti F, Facciolo F, Mottolese M, Milella M, Nisticò P.
Bria E, et al. Among authors: iapicca p.
Oncotarget. 2014 Nov 30;5(22):11054-63. doi: 10.18632/oncotarget.2609.
Oncotarget. 2014.
PMID: 25373410
Free PMC article.
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The pattern of hMENA isoforms is regulated by TGF-β1 in pancreatic cancer and may predict patient outcome.
Melchionna R, Iapicca P, Di Modugno F, Trono P, Sperduti I, Fassan M, Cataldo I, Rusev BC, Lawlor RT, Diodoro MG, Milella M, Grazi GL, Bissell MJ, Scarpa A, Nisticò P.
Melchionna R, et al. Among authors: iapicca p.
Oncoimmunology. 2016 Aug 12;5(12):e1221556. doi: 10.1080/2162402X.2016.1221556. eCollection 2016.
Oncoimmunology. 2016.
PMID: 28123868
Free PMC article.
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Molecular and genetic bases of pancreatic cancer.
Vaccaro V, Gelibter A, Bria E, Iapicca P, Cappello P, Di Modugno F, Pino MS, Nuzzo C, Cognetti F, Novelli F, Nistico P, Milella M.
Vaccaro V, et al. Among authors: iapicca p.
Curr Drug Targets. 2012 Jun;13(6):731-43. doi: 10.2174/138945012800564077.
Curr Drug Targets. 2012.
PMID: 22458519
Free article.
Review.
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Reliability and reproducibility among different platforms for tumour BRCA testing in ovarian cancer: a study of the Italian NGS Network.
Fumagalli C, Guerini-Rocco E, Buttitta F, Iapicca P, You W, Mauri M, Felicioni L, Troncone G, Malapelle U, Scarpa A, Zamboni G, Calistri D, Barberis M, Marchetti A.
Fumagalli C, et al. Among authors: iapicca p.
J Clin Pathol. 2021 Oct;74(10):668-672. doi: 10.1136/jclinpath-2020-206800. Epub 2020 Oct 5.
J Clin Pathol. 2021.
PMID: 33020174
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Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework.
Tenedini E, Celestini F, Iapicca P, Marino M, Castellano S, Artuso L, Biagiarelli F, Cortesi L, Toss A, Barbieri E, Roncucci L, Pedroni M, Manfredini R, Luppi M, Trenti T, Tagliafico E.
Tenedini E, et al. Among authors: iapicca p.
Diagnosis (Berl). 2021 Jun 16;9(1):115-122. doi: 10.1515/dx-2021-0051.
Diagnosis (Berl). 2021.
PMID: 34142509
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The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein.
Laforgia N, De Cosmo L, Palumbo O, Ranieri C, Sesta M, Capodiferro D, Pantaleo A, Iapicca P, Lastella P, Capozza M, Schettini F, Bukvic N, Bagnulo R, Resta N.
Laforgia N, et al. Among authors: iapicca p.
Genes (Basel). 2020 Dec 18;11(12):1519. doi: 10.3390/genes11121519.
Genes (Basel). 2020.
PMID: 33353066
Free PMC article.
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