Tritto Viviana

Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes / V. Tritto, P. Bettinaglio, E. Mangano, C. Cesaretti, F. Marasca, C. Castronovo, R. Bordoni, C. Battaglia, V. Saletti, V. Ranzani, B. Bodega, M. Eoli, F. Natacci, P. Riva. - In: HUMAN GENETICS. - ISSN 1432-1203. - 143:6(2024 Jun), pp. 775-795. [10.1007/s00439-024-02683-0]

Expression analysis of NF1-mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR / P. Bettinaglio, V. Tritto, R. Paterra, M. Eoli, P. Riva. - In: ANNALS OF HUMAN GENETICS. - ISSN 1469-1809. - 88:3(2024 May), pp. 183-193. [10.1111/ahg.12540]

Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes / V. Tritto, D. Capitanio, C. Gelfi, P. Riva. - In: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. - ISSN 1422-0067. - 24:4(2023 Feb 17), pp. 4035.1-4035.14. [10.3390/ijms24044035]

New insights into the molecular basis of spinal neurofibromatosis type 1 / P. Bettinaglio, E. Mangano, V. Tritto, R. Bordoni, R. Paterra, A. Borghi, M. Volontè, C. Battaglia, V. Saletti, C. Cesaretti, F. Natacci, M.A.B. Melone, M. Eoli, P. Riva. - In: EUROPEAN JOURNAL OF HUMAN GENETICS. - ISSN 1018-4813. - (2023), pp. 1-8. [Epub ahead of print] [10.1038/s41431-023-01377-x]

Deregulated expression of polycomb repressive complex 2 target genes in a NF1 patient with microdeletion generating the RNF135-SUZ12 chimeric gene / V. Tritto, F. Grilli, D. Milani, P.V. Riva. - In: NEUROGENETICS. - ISSN 1364-6745. - (2023), pp. 1-8. [Epub ahead of print] [10.1007/s10048-023-00718-8]