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Titolo Data di pubblicazione Autore(i) File
Epigenetic bivalent marking is permissive to the synergy of HDAC and PARP inhibitors on TXNIP expression in breast cancer cells 1-gen-2015 Baldan, Federica; Mio, Catia; Lavarone, Elisa; DI LORETO, Carla; Puglisi, Fabio; Damante, Giuseppe; Puppin, Cinzia
Synergy between HDAC and PARP Inhibitors on Proliferation of a Human Anaplastic Thyroid Cancer-Derived Cell Line 1-gen-2015 Baldan, Federica; Mio, Catia; Allegri, Lorenzo; Puppin, Cinzia; Russo, Diego; Filetti, Sebastiano; Damante, Giuseppe
Identification of tumorigenesis-related mRNAs associated with RNA-binding protein HuR in thyroid cancer cells 1-gen-2016 Baldan, Federica; Mio, Catia; Allegri, Lorenzo; Conzatti, Ketty; Toffoletto, Barbara; Puppin, Cinzia; Radovic, Slobodanka; Vascotto, Carlo; Russo, Diego; DI LORETO, Carla; Damante, Giuseppe
MCM5 as a target of BET inhibitors in thyroid cancer cells 1-gen-2016 Mio, Catia; Lavarone, Elisa; Conzatti, Ketty; Baldan, Federica; Toffoletto, Barbara; Puppin, Cinzia; Filetti, Sebastiano; Durante, Cosimo; Russo, Diego; Orlacchio, Arturo; Di Cristofano, Antonio; DI LORETO, Carla; Damante, Giuseppe
Effects of BP-14, a novel cyclin-dependent kinase inhibitor, on anaplastic thyroid cancer cells 1-gen-2016 Allegri, Lorenzo; Baldan, Federica; Mio, Catia; Puppin, Cinzia; Russo, Diego; Kry͉tof, Vladimir; Damante, Giuseppe
Expression of PAX8 target genes in papillary thyroid carcinoma 1-gen-2016 Rosignolo, Francesca; Sponziello, Marialuisa; Durante, Cosimo; Puppin, Cinzia; Mio, Catia; Baldan, Federica; DI LORETO, Carla; Russo, Diego; Filetti, Sebastiano; Damante, Giuseppe
A polymorphic GGC repeat in the NPAS2 gene and its association with melanoma 1-gen-2017 Franzoni, Alessandra; Markova-Car, Elitza; Dević-Pavlić, Sanja; Jurišić, Davor; Puppin, Cinzia; Mio, Catia; De Luca, Marila; Petruz, Giulia; Damante, Giuseppe; Pavelić, Sandra Kraljević
Analysis of the biological mechanisms de-regulated after pharmacological BET inhibition in a model of anaplastic thyroid cancer 29-mar-2017 Mio, Catia
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches 1-gen-2018 Baldan, Federica; Mio, Catia; Allegri, Lorenzo; Passon, Nadia; Lepore, Saverio M.; Russo, Diego; Damante, Giuseppe
Targeting post-translational histone modifications for the treatment of non-medullary thyroid cancer 1-gen-2018 Celano, Marilena; Mio, Catia; Sponziello, Marialuisa; Verrienti, Antonella; Bulotta, Stefania; Durante, Cosimo; Damante, Giuseppe; Russo, Diego
Effects of nutraceuticals on anaplastic thyroid cancer cells 1-gen-2018 Allegri, Lorenzo; Rosignolo, Francesca; Mio, Catia; Baldan, Federica; Damante, Giuseppe; Filetti, Sebastiano
Effects of HuR downregulation on anaplastic thyroid cancer cells 1-gen-2018 Allegri, L.; Mio, C.; Russo, D.; Filetti, S.; Baldan, F.
BET bromodomain inhibitor JQ1 modulates microRNA expression in thyroid cancer cells 1-gen-2018 Mio, Catia; Conzatti, Ketty; Baldan, Federica; Allegri, Lorenzo; Sponziello, Marialuisa; Rosignolo, Francesca; Russo, Diego; Filetti, Sebastiano; Damante, Giuseppe
Molecular defects in thyroid dysgenesis 1-gen-2019 Mio, C.; Grani, G.; Durante, C.; Damante, G.
BET proteins regulate homologous recombination-mediated DNA repair: BRCAness and implications for cancer therapy 1-gen-2019 Mio, Catia; Gerratana, Lorenzo; Bolis, Marco; Caponnetto, Federica; Zanello, Andrea; Barbina, Mattia; Di Loreto, Carla; Garattini, Enrico; Damante, Giuseppe; Puglisi, Fabio
Inhibition of APE1-endonuclease activity affects cell metabolism in colon cancer cells via a p53-dependent pathway 1-gen-2019 Codrich, Marta; Comelli, Marina; Malfatti, Matilde Clarissa; Mio, Catia; Ayyildiz, Dilara; Zhang, Chi; Kelley, Mark R; Terrosu, Giovanni; Pucillo, Carlo E M; Tell, Gianluca
Human telomerase reverse transcriptase in papillary thyroid cancer: gene expression, effects of silencing and regulation by BET inhibitors in thyroid cancer cells 1-gen-2019 Maggisano, Valentina; Celano, Marilena; Lepore, Saverio Massimo; Sponziello, Marialuisa; Rosignolo, Francesca; Pecce, Valeria; Verrienti, Antonella; Baldan, Federica; Mio, Catia; Allegri, Lorenzo; Maranghi, Marianna; Falcone, Rosa; Damante, Giuseppe; Russo, Diego; Bulotta, Stefania
Biological and molecular effects of bromodomain and extra-terminal (BET) inhibitors JQ1, IBET-151, and IBET-762 in OSCC cells 1-gen-2019 Baldan, Federica; Allegri, Lorenzo; Lazarevic, Milos; Mio, Catia; Milosevic, Maja; Damante, Giuseppe; Milasin, Jelena
Reading cancer: Chromatin readers as druggable targets for cancer treatment 1-gen-2019 Mio, Catia; Bulotta, Stefania; Russo, Diego; Damante, Giuseppe
A Streamlined Approach to Rapidly Detect SARS-CoV-2 Infection Avoiding RNA Extraction: Workflow Validation 1-gen-2020 Mio, C.; Cifu, A.; Marzinotto, S.; Bergamin, N.; Caldana, C.; Cattarossi, S.; Cmet, S.; Cussigh, A.; Martinella, R.; Zucco, J.; Verardo, R.; Schneider, C.; Marcon, B.; Zampieri, S.; Pipan, C.; Curcio, F.
Exploring the molecular insights of concurrent composite mucoepidermoid carcinoma and papillary thyroid carcinoma 1-gen-2020 Falcone, Rosa; Sponziello, Marialuisa; Carletti, Raffella; Di Gioia, Cira; Nardi, Francesco; Mio, Catia; Pecce, Valeria; Abballe, Luana; Grani, Giorgio; Ramundo, Valeria; Damante, Giuseppe; Durante, Cosimo; Filetti, Marco; Roberto, Michela; Marchetti, Paolo; Verrienti, Antonella
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers 1-gen-2020 Mio, C.; Passon, N.; Baldan, F.; Bregant, E.; Monaco, E.; Mancini, L.; Demori, E.; Damante, G.
BAZ1B is a candidate gene responsible for hypothyroidism in Williams syndrome 1-gen-2020 Allegri, L.; Baldan, F.; Mio, C.; De Felice, M.; Amendola, E.; Damante, G.
Missense NR2F1 variant in monozygotic twins affected with the Bosch–Boonstra–Schaaf optic atrophy syndrome 1-gen-2020 Mio, C.; Fogolari, F.; Pezzoli, L.; D'Elia, A. V.; Iascone, M.; Damante, G.
Correction to: Exploring the molecular insights of concurrent composite mucoepidermoid carcinoma and papillary thyroid carcinoma (Endocrine, (2020), 10.1007/s12020-020-02221-8) 1-gen-2020 Falcone, R.; Sponziello, M.; Carletti, R.; Di Gioia, C.; Nardi, F.; Mio, C.; Pecce, V.; Abballe, L.; Grani, G.; Ramundo, V.; Damante, G.; Durante, C.; Filetti, M.; Roberto, M.; Marchetti, P.; Verrienti, A.
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 1-gen-2020 Mio, C.; Allegri, L.; Passon, N.; Bregant, E.; Demori, E.; Franzoni, A.; Driul, D.; Riccio, A.; Damante, G.; Baldan, F.
Nanoparticles loaded with the BET inhibitor JQ1 block the growth of triple negative breast cancer cells in vitro and in vivo 1-gen-2020 Maggisano, V.; Celano, M.; Malivindi, R.; Barone, I.; Cosco, D.; Mio, C.; Mignogna, C.; Panza, S.; Damante, G.; Fresta, M.; Ando, S.; Russo, D.; Catalano, S.; Bulotta, S.
Monitoring the SPREAD of the SARS-CoV-2 lineage B.1.621 in Udine, Italy 1-gen-2021 Mio, Catia; Dal Secco, Chiara; Marzinotto, Stefania; Pipan, Corrado; Sozio, Emanuela; Tascini, Carlo; Damante, Giuseppe; Curcio, Francesco
A novel de novo HDAC8 missense mutation causing Cornelia de Lange syndrome 1-gen-2021 Mio, C.; Passon, N.; Fogolari, F.; Cesario, C.; Novelli, A.; Pittini, C.; Damante, G.
Integrated multi-omics analyses on patient-derived CRC organoids highlight altered molecular pathways in colorectal cancer progression involving PTEN 1-gen-2021 Codrich, M.; Dalla, E.; Mio, C.; Antoniali, G.; Malfatti, M. C.; Marzinotto, S.; Pierobon, M.; Baldelli, E.; Di Loreto, C.; Damante, G.; Terrosu, G.; Pucillo, C. E. M.; Tell, G.
Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia 1-gen-2021 Mio, C.; Dal Secco, C.; Marzinotto, S.; Bruno, C.; Pimpo, S.; Betto, E.; Bertoni, M.; Pipan, C.; Sozio, E.; Tascini, C.; Damante, G.; Curcio, F.
Pro‐inflammatory microenvironment modulates the transfer of mutated tp53 mediated by tumor exosomes 1-gen-2021 Domenis, R.; Cifu, A.; Mio, C.; Fabris, M.; Curcio, F.
Rare germline variants in DNA repair-related genes are accountable for papillary thyroid cancer susceptibility 1-gen-2021 Mio, C.; Verrienti, A.; Pecce, V.; Sponziello, M.; Damante, G.
A novel de novo NIPA1 missense mutation associated to hereditary spastic paraplegia 1-gen-2021 Fabbro, D.; Mio, C.; Fogolari, F.; Damante, G.
Validation of a One-Step Reverse Transcription-Droplet Digital PCR (RT-ddPCR) Approach to Detect and Quantify SARS-CoV-2 RNA in Nasopharyngeal Swabs 1-gen-2021 Mio, Catia; Cifu', Adriana; Marzinotto, Stefania; Marcon, Barbara; Pipan, Corrado; Damante, Giuseppe; Curcio, Francesco
NK2 homeobox gene cluster: Functions and roles in human diseases 1-gen-2022 Mio, C.; Baldan, F.; Damante, G.
Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structure 1-gen-2022 Franzoni, A.; Baldan, F.; Passon, N.; Mio, C.; Driul, D.; Cogo, P.; Fogolari, F.; D'Aurizio, F.; Damante, G.
Challenges in promoter methylation analysis in the new era of translational oncology: a focus on liquid biopsy 1-gen-2022 Mio, C.; Damante, G.
Role of m6A RNA Methylation in Thyroid Cancer Cell Lines 1-gen-2022 Allegri, L.; Baldan, F.; Molteni, E.; Mio, C.; Damante, G.
Monoallelic variants resulting in substitutions of MAB21L1 Arg51 Cause Aniridia and microphthalmia 1-gen-2022 Hall, H. N.; Bengani, H.; Hufnagel, R. B.; Damante, G.; Ansari, M.; Marsh, J. A.; Grimes, G. R.; von Kriegsheim, A.; Moore, D.; Mckie, L.; Rahmat, J.; Mio, C.; Blyth, M.; Keng, W. T.; Islam, L.; Mcentargart, M.; Mannens, M. M.; Van Heyningen, V.; Rainger, J.; Brooks, B. P.; Fitzpatrick, D. R.
Identification of Exosomal microRNAs and Their Targets in Papillary Thyroid Cancer Cells 1-gen-2022 Maggisano, Valentina; Capriglione, Francesca; Verrienti, Antonella; Celano, Marilena; Gagliardi, Agnese; Bulotta, Stefania; Sponziello, Marialuisa; Mio, Catia; Pecce, Valeria; Durante, Cosimo; Damante, Giuseppe; Russo, Diego
Brain Endothelial Cells Activate Neuroinflammatory Pathways in Response to Early Cerebral Small Vessel Disease (CSVD) Patients’ Plasma 1-gen-2023 Cifu', A.; Janes, F.; Mio, C.; Pessa, M. E.; Garbo, R.; Curcio, F.; Valente, M.; Fabris, M.; Domenis, R.
Somatic genomic imbalances in ‘tumour-free’ surgical margins of oral cancer 1-gen-2023 Baldan, F.; Gnan, C.; Lazarevic, M.; Nikolic, N.; Mio, C.; Tepavcevic, Z.; Robiony, M.; Milasin, J.; Damante, G.
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases 1-gen-2024 Zucco, J.; Baldan, F.; Allegri, L.; Bregant, E.; Passon, N.; Franzoni, A.; D'Elia, A. V.; Faletra, F.; Damante, G.; Mio, C.
RNA Profile of Cell Bodies and Exosomes Released by Tumorigenic and Non-Tumorigenic Thyroid Cells 1-gen-2024 Maggisano, V.; Capriglione, F.; Mio, C.; Bulotta, S.; Damante, G.; Russo, D.; Celano, M.
Filamin C (FLNC) truncating mutation in a fatal arrhythmogenic left ventricular cardiomyopathy (ALVC) 1-gen-2024 Simonit, F.; Da Broi, U.; D'Elia, A. V.; Fabbro, D.; Mio, C.; Bussani, R.; Pinamonti, M.; Desinan, L.
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