Sfoglia per Autore
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers
2020-01-01 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
2020-01-01 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
2020-01-01 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)
2020-01-01 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
2020-01-01 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
2020-01-01 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.
Exploring the molecular insights of concurrent composite mucoepidermoid carcinoma and papillary thyroid carcinoma
2020-01-01 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
Monitoring the SPREAD of the SARS-CoV-2 lineage B.1.621 in Udine, Italy
2021-01-01 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
2021-01-01 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
2021-01-01 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
2021-01-01 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
2021-01-01 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
2021-01-01 Mio, C.; Verrienti, A.; Pecce, V.; Sponziello, M.; Damante, G.
A novel de novo NIPA1 missense mutation associated to hereditary spastic paraplegia
2021-01-01 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
2021-01-01 Mio, Catia; Cifu', Adriana; Marzinotto, Stefania; Marcon, Barbara; Pipan, Corrado; Damante, Giuseppe; Curcio, Francesco
NK2 homeobox gene cluster: Functions and roles in human diseases
2022-01-01 Mio, C.; Baldan, F.; Damante, G.
Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structure
2022-01-01 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
2022-01-01 Mio, C.; Damante, G.
Role of m6A RNA Methylation in Thyroid Cancer Cell Lines
2022-01-01 Allegri, L.; Baldan, F.; Molteni, E.; Mio, C.; Damante, G.
Monoallelic variants resulting in substitutions of MAB21L1 Arg51 Cause Aniridia and microphthalmia
2022-01-01 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.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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. | |
| 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 | |
| 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. |
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