TRITTO, VIVIANA

TRITTO, VIVIANA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes 2023 Tritto, VivianaCapitanio, DanieleGelfi, CeciliaRiva, Paola Article (author) -
Deregulated expression of polycomb repressive complex 2 target genes in a NF1 patient with microdeletion generating the RNF135-SUZ12 chimeric gene 2023 Viviana TrittoFederico GrilliDonatella MilaniPaola Riva Article (author) -
Expression analysis of NF1-mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR 2023 Bettinaglio, PaolaTritto, VivianaRiva, Paola + Article (author) -
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort 2023 Paola BettinaglioEleonora ManganoViviana TrittoClaudia CesarettiRoberta BordoniMarco MoscatelliPaola Riva + Article (author) -
New insights into the molecular basis of spinal neurofibromatosis type 1 2023 Bettinaglio, PaolaMangano, EleonoraTritto, VivianaBordoni, RobertaBattaglia, CristinaCesaretti, ClaudiaRiva, Paola + Article (author) -
Position effect and of modifier Ras pathway genes in Neurofibromatosis type I microdeletion syndrome 2022 V. TrittoC. BattagliaP. Riva + Article (author) -
Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes 2022 Tritto, VivianaRusconi, FrancescoRiva, Paola + Article (author) -
Preclinical and clinical evidence on the approach-avoidance conflict evaluation as an integrative tool for psychopathology 2022 Rusconi, FForastieri, CTritto, VBattaglioli, E + Article (author) -
Role of hypomorphic variants in variable expressivity of Noonan syndrome 2022 V. TrittoC. BattagliaP. Riva + Article (author) -
NF1 Gene Mutation Mediates Neuronal Signaling De-Regulation Triggering Pediatric Optic Glioma Development: Another Small Step towards a Cure of NF1 Disorder? 2021 P. RivaV. Tritto Article (author) -
Prevalence of NF1 missense mutations and candidate modifier genes in 12 familial and 15 sporadic spinal neurofibromatosis patients 2020 P. RivaV. TrittoC. Battaglia + Article (author) -
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 Tritto, VivianaFerrari, LucaZuccotti, PaolaRiva, Paola + Article (author) -