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Page 1
Testing calpain inhibition in tumor endothelial cells: novel targetable biomarkers against glioblastoma malignancy.
Guarnaccia L, Navone SE, Begani L, Barilla E, Garzia E, Campanella R, Miozzo M, Fontana L, Alotta G, Cordiglieri C, Gaudino C, Schisano L, Ampollini A, Riboni L, Locatelli M, Marfia G. Guarnaccia L, et al. Among authors: fontana l. Front Oncol. 2024 Aug 2;14:1355202. doi: 10.3389/fonc.2024.1355202. eCollection 2024. Front Oncol. 2024. PMID: 39156707 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.
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome.
Paganini L, Pesenti C, Milani D, Fontana L, Motta S, Sirchia SM, Scuvera G, Marchisio P, Esposito S, Cinnante CM, Tabano SM, Miozzo MR. Paganini L, et al. Among authors: fontana l. Am J Med Genet A. 2018 Jun;176(6):1427-1431. doi: 10.1002/ajmg.a.38704. Epub 2018 Apr 16. Am J Med Genet A. 2018. PMID: 29663667
877 results