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The Genetic Landscape of Human Glioblastoma and Matched Primary Cancer Stem Cells Reveals Intratumour Similarity and Intertumour Heterogeneity.
Pesenti C, Navone SE, Guarnaccia L, Terrasi A, Costanza J, Silipigni R, Guarneri S, Fusco N, Fontana L, Locatelli M, Rampini P, Campanella R, Tabano S, Miozzo M, Marfia G. Pesenti C, et al. Among authors: fontana l. Stem Cells Int. 2019 Mar 7;2019:2617030. doi: 10.1155/2019/2617030. eCollection 2019. Stem Cells Int. 2019. PMID: 30984267 Free PMC article.
Differential signature of the centrosomal MARK4 isoforms in glioma.
Magnani I, Novielli C, Fontana L, Tabano S, Rovina D, Moroni RF, Bauer D, Mazzoleni S, Colombo EA, Tedeschi G, Monti L, Porta G, Bosari S, Frassoni C, Galli R, Bello L, Larizza L. Magnani I, et al. Among authors: fontana l. Anal Cell Pathol (Amst). 2011;34(6):319-38. doi: 10.3233/ACP-2011-0031. Anal Cell Pathol (Amst). 2011. PMID: 22156016 Free PMC article.
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion.
Fontana L, Tabano S, Bonaparte E, Marfia G, Pesenti C, Falcone R, Augello C, Carlessi N, Silipigni R, Guerneri S, Campanella R, Caroli M, Sirchia SM, Bosari S, Miozzo M. Fontana L, et al. J Neuropathol Exp Neurol. 2016 Aug;75(8):791-800. doi: 10.1093/jnen/nlw052. Epub 2016 Jun 26. J Neuropathol Exp Neurol. 2016. PMID: 27346749 Free PMC article.
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies.
Azzollini J, Pesenti C, Ferrari L, Fontana L, Calvello M, Peissel B, Portera G, Tabano S, Carcangiu ML, Riva P, Miozzo M, Manoukian S. Azzollini J, et al. Among authors: fontana l. PLoS One. 2017 Feb 15;12(2):e0171663. doi: 10.1371/journal.pone.0171663. eCollection 2017. PLoS One. 2017. PMID: 28199346 Free PMC article.
Fragile X syndrome: a review of clinical and molecular diagnoses.
Ciaccio C, Fontana L, Milani D, Tabano S, Miozzo M, Esposito S. Ciaccio C, et al. Among authors: fontana l. Ital J Pediatr. 2017 Apr 19;43(1):39. doi: 10.1186/s13052-017-0355-y. Ital J Pediatr. 2017. PMID: 28420439 Free PMC article. Review.
Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status.
Pesenti C, Paganini L, Fontana L, Veniani E, Runza L, Ferrero S, Bosari S, Menghi M, Marfia G, Caroli M, Silipigni R, Guerneri S, Tabano S, Miozzo M. Pesenti C, et al. Among authors: fontana l. Oncotarget. 2017 Jul 8;8(34):57134-57148. doi: 10.18632/oncotarget.19103. eCollection 2017 Aug 22. Oncotarget. 2017. PMID: 28915660 Free PMC article.
873 results