RIVA, PAOLA VANDA
RIVA, PAOLA VANDA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
Deregulated expression of polycomb repressive complex 2 target genes in a NF1 patient with microdeletion generating the RNF135-SUZ12 chimeric gene
2023 V. Tritto, F. Grilli, D. Milani, P.V. Riva
Expression analysis of NF1-mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR
2023 P. Bettinaglio, V. Tritto, R. Paterra, M. Eoli, P. Riva
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators?
2023 S. Redaelli, F.R. Grati, V. Tritto, G. Giannuzzi, M.P. Recalcati, E. Sala, N. Villa, F. Crosti, G. Roversi, F. Malvestiti, V. Zanatta, E. Repetti, O. Rodeschini, C. Valtorta, I. Catusi, L. Romitti, E. Martinoli, D. Conconi, L. Dalprà, M. Lavitrano, P. Riva, A. Bentivegna
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes
2023 V. Tritto, D. Capitanio, C. Gelfi, P. Riva
New insights into the molecular basis of spinal neurofibromatosis type 1
2023 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
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
2023 R. Paterra, P. Bettinaglio, A. Borghi, E. Mangano, V. Tritto, C. Cesaretti, C. Schettino, R. Bordoni, C. Santoro, S. Avignone, M.E.M. Moscatelli, M. Anna Beatrice Melone, V. Saletti, G. Piluso, F. Natacci, P.V. Riva, M. Eoli
Position effect and of modifier Ras pathway genes in Neurofibromatosis type I microdeletion syndrome
2022 P. Bettinaglio, V. Tritto, E. Mangano, R. Bordoni, C. Castronuovo, M. Volontè, C. Cesaretti, G.A. Cagnoli, C. Battaglia, V. Saletti, D. Bianchessi, F. Natacci, M. Eoli, P. Riva
Role of hypomorphic variants in variable expressivity of Noonan syndrome
2022 V. Tritto, E. Mangano, M.T. Bonati, P. Bettinaglio, C. Battaglia, R. Bordoni, P. Riva
Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes
2022 V. Tritto, M. Eoli, R. Paterra, S. Redaelli, M. Moscatelli, F. Rusconi, P. Riva
NF1 Gene Mutation Mediates Neuronal Signaling De-Regulation Triggering Pediatric Optic Glioma Development: Another Small Step towards a Cure of NF1 Disorder?
2021 P. Riva, V. Tritto
Human chromosome 18 and acrocentrics : a dangerous liaison
2021 N. Villa, S. Redaelli, E. Sala, D. Conconi, L. Romitti, E. Manfredini, F. Crosti, G. Roversi, M. Lavitrano, O. Rodeschini, M. Paola Recalcati, P. Rocco, L. Dalprà, P.V. Riva, A. Bentivegna
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?
2020 L. Ferrari, E. Mangano, M.T. Bonati, I. Monterosso, D. Capitanio, F. Chiappori, I. Brambilla, C. Gelfi, C. Battaglia, R. Bordoni, P. Riva
Instability of short arm of acrocentric chromosomes : Lesson from non-acrocentric satellited chromosomes. Report of 24 unrelated cases
2020 S. Redaelli, D. Conconi, N. Villa, E. Sala, F. Crosti, C. Corti, I. Catusi, M. Garzo, L. Romitti, E. Martinoli, A. Patrizi, R. Malgara, M.P. Recalcati, L. Dalprà, M. Lavitrano, P. Riva, G. Roversi, A. Bentivegna
Prevalence of NF1 missense mutations and candidate modifier genes in 12 familial and 15 sporadic spinal neurofibromatosis patients
2020 P. Riva, E. Mangano, C. Cesaretti, P. Bettinaglio, R. Bordoni, V. Tritto, C. Battaglia, V. Saletti, D. Bianchessi, M. Marina Melone, C. Schettino, F. Natacci, M. Eoli
HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal muscles
2019 L. Ferrari, C. Bragato, L. Brioschi, M. Spreafico, S. Esposito, A. Pezzotta, F. Pizzetti, A. Moreno-Fortuny, G. Bellipanni, A. Giordano, P. Riva, F. Frabetti, P. Viani, G. Cossu, M. Mora, A. Marozzi, A. Pistocchi
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients
2019 V. Tritto, L. Ferrari, S. Esposito, P. Zuccotti, D. Bianchessi, F. Natacci, V. Saletti, M. Eoli, P. Riva
NIPBL: a new player in myeloid cells differentiation
2019 M. Mazzola, G. Deflorian, A. Pezzotta, L. Ferrari, G. Fazio, E. Bresciani, C. Saitta, L. Ferrari, M. Fumagalli, M. Parma, F. Marasca, B. Bodega, P. Riva, F. Cotelli, A. Biondi, A. Marozzi, G. Cazzaniga, A. Pistocchi
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases
2019 P. Riva, C. Battaglia, M. Venturin
Introduzione al genoma umano
2018 A. Marozzi, M. Capasso, L. Ferrari, B. Franco, A. Iolascon, L. Migliore, M.R. Miozzo, A. Pizzuti, B. Porfirio, N. Resta, P.V. Riva, S.M. Sirchia, A. Turco, O. Zuffardi
NIPBL a new player with NPMc+ in the onset of acute myeloid leukemia
2018 M. Mazzola, G. Fazio, G. De florian, L. Ferrari, M. Spreafico, C. Saitta, L. Ferrari, E. Bresciani, A. Biondi, F. Cotelli, M. Fumagalli, M. Parma, P. Riva, A. Marozzi, G. Cazzaniga, A. Pistocchi