Sfoglia per Afferenza ROMA - Dipartimento di Scienze della vita e sanità pubblica
NOVEL MEMBERS OF THE PLEXIN FAMILY AND USES THEREOF
2000 Artigiani, Stefania; COMOGLIO Paolo, M; GOODMAN Corey, S; TESSIER-LAVIGNE, Marc; Tamagnone, Luca
A novel MEN1 pathogenic variant in an Italian patient with multiple endocrine neoplasia type 1
2020 Corsello, Andrea; Bruno, Carmine; Rizza, Roberta; Concolino, Paola; Papi, Giampaolo; Pontecorvi, Alfredo; Rindi, Guido; Paragliola, Rosa Maria
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer
2005 Lucci-Cordisco, E; Zollino, Marcella; Baglioni, S; Mancuso, I; Lecce, R; Gurrieri, Fiorella; Crucitti, Antonio; Papi, L; Neri, G; Genuardi, Maurizio
A novel nonsense PTH1R variant shows incomplete penetrance of primary failure of eruption: a case report
2019 Grippaudo, Cristina; Cafiero, Concetta; D'Apolito, Isabella; Re, Agnese; Genuardi, Maurizio; Chiurazzi, Pietro; Frazier-Bowers, Sylvia A.
Novel Osteointegrative Sr-Substituted Apatitic Cements Enriched with Alginate
2016 Sprio, Simone; Dapporto, Massimiliano; Montesi, Monica; Panseri, Silvia; Lattanzi, Wanda; Pola, Enrico; Logroscino, Giandomenico; Tampieri, Anna
A Novel Prognostic Marker for Primary CNS Lymphoma: Lactate Dehydrogenase-to-Lymphocyte Ratio Improves Stratification of Patients Within the Low and Intermediate MSKCC Risk Groups
2021 Gao, Yuting; Wei, Li; Jin Kim, Seok; Wang, Liang; He, Yingzhi; Zheng, Yanfang; Bertero, Luca; Pellerino, Alessia; Cassoni, Paola; Tamagnone, Luca; Katharina Theresa, Prochazka; Deutsch, Alexander; Zhan, Huien; Lai, Jing; Wang, Yao; You, Hua
A novel prognostic model based on pretreatment serum albumin and ECOG PS for primary CNS lymphoma: an international, multi-center study
2023 Wei, Li; Gao, Yuting; Theresa Prochazka, Katharina; Liu, Rongqiu; Wang, Liang; Liu, Boyang; He, Yingzhi; Bertero, Luca; Pellerino Paola Cassoni, Alessia; Tamagnone, Luca; J Deutsch, Alexander; Zhan, Huien; Lai, Jing; Jin Kim, Seok; You, Hua
A novel self-lipid antigen targets human T cells against CD1c(+) leukemias
2014 Lepore, Marco; de Lalla, Claudia; Gundimeda, S Ramanjaneyulu; Gsellinger, Heiko; Consonni, Michela; Garavaglia, Claudio; Sansano, Sebastiano; Piccolo, Francesco; Scelfo, Andrea; Häussinger, Daniel; Montagna, Daniela; Locatelli, Franco; Bonini, Chiara; Bondanza, Attilio; Forcina, Alessandra; Li, Zhiyuan; Ni, Guanghui; Ciceri, Fabio; Jenö, Paul; Xia, Chengfeng; Mori, Lucia; Dellabona, Paolo; Casorati, Giulia; De Libero, Gennaro
Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy
2022 Bosco, Luca; Leone, Daniela; Costa Comellas, Laura; Monforte, Mauro; Pane, Marika; Mercuri, Eugenio Maria; Bertini, Enrico Silvio; D'Amico, Adele; Fattori, Fabiana
Novel Therapeutic Approaches to Familial HLH (Emapalumab in FHL)
2020 Merli, P.; Algeri, M.; Gaspari, S.; Locatelli, Franco
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis
2021 Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, Amelia; Marangi, Giuseppe; Martello, Francesco; Bisogni, Giulia; Meleo, Emiliana; Colavito, Davide; Del Giudice, Elda; Patanella, Agata Katia; Bernardo, Daniela; Romano, Angela; Zollino, Marcella; Sabatelli, Mario
De novo a-to-i rna editing discovery in lncrna
2020 Silvestris, D. A.; Scopa, C.; Hanchi, S.; Locatelli, Franco; Gallo, A.
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
2012 Heinzen, El; Swoboda, Kj; Hitomi, Y; Gurrieri, Fiorella; Tiziano, Francesco Danilo; Nicole, S; Fontaine, B; De Vries, B; Walley, Nm; Heavin, S; Panagiotakaki, E; Koelewijn, S; Kamphorst, J; Geilenkirchen, M; Pelzer, N; Laan, L; Haan, J; Ferrari, Mirella; Van Den Maagdenberg, A; Fiori, S; Abiusi, Emanuela; Di Pietro, Lorena; Sweney, Mt; Newcomb, Tm; Viollet, L; Huff, C; Jorde, Lb; Reyna, Sp; Murphy, Kj; Shianna, Kv; Gumbs, Ce; Little, L; Silver, K; Ptáček, Lj; Haan, J; Herke, S Gk; Whitelaw, Cm; Webb, D; Lynch, Bj; Uldall, P; King, Md; Scheffer, Ie; Neri, Giovanni; Arzimanoglou, A; Sisodiya, Sm; Mikati, Ma; Goldstein, Db
De novo partial 13q22-q34 trisomy with typical neurological and immunological findings: A case report with new genetic insights
2021 Brogna, Claudia; Milano, Valentina; Brogna, B.; Cristiano, Lara; Rovere, Giuseppe; De Sanctis, Roberto; Romeo, Domenico Marco; Mercuri, Eugenio Maria; Zampino, Giuseppe
De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides–Baraitser syndrome
2020 Cappuccio, G.; Sayou, C.; Tanno, P. L.; Tisserant, E.; Bruel, A. -L.; Kennani, S. E.; Sa, J.; Low, K. J.; Dias, C.; Havlovicova, M.; Hancarova, M.; Eichler, E. E.; Devillard, F.; Moutton, S.; Van-Gils, J.; Dubourg, C.; Odent, S.; Gerard, B.; Piton, A.; Yamamoto, T.; Okamoto, N.; Firth, H.; Metcalfe, K.; Moh, A.; Chapman, K. A.; Aref-Eshghi, E.; Kerkhof, J.; Torella, A.; Nigro, V.; Perrin, L.; Piard, J.; Le Guyader, G.; Jouan, T.; Thauvin-Robinet, C.; Duffourd, Y.; George-Abraham, J. K.; Buchanan, C. A.; Williams, D.; Kini, U.; Wilson, K.; Nigro, V.; Brunetti-Pierri, N.; Casari, G.; Cappuccio, G.; Torella, A.; Pinelli, M.; Musacchia, F.; Mutarelli, M.; Carrella, D.; Vitiello, G.; Capra, V.; Parenti, G.; Leuzzi, V.; Selicorni, A.; Maitz, S.; Banfi, S.; Zollino, Marcella; Montomoli, M.; Milani, D.; Romano, C.; Tummolo, A.; De Brasi, D.; Coppola, A.; Santoro, C.; Peron, A.; Pantaleoni, C.; Castello, R.; D'Arrigo, S.; Sousa, S. B.; Hennekam, R. C. M.; Sadikovic, B.; Thevenon, J.; Govin, J.; Vitobello, A.; Brunetti-Pierri, N.
De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment
2020 Rodger, C.; Flex, E.; Allison, R. J.; Sanchis-Juan, A.; Hasenahuer, M. A.; Cecchetti, S.; French, C. E.; Edgar, J. R.; Carpentieri, G.; Ciolfi, A.; Pantaleoni, F.; Bruselles, A.; Onesimo, Roberta; Zampino, Giuseppe; Marcon, F.; Siniscalchi, E.; Lees, M.; Krishnakumar, D.; Mccann, E.; Yosifova, D.; Jarvis, J.; Kruer, M. C.; Marks, W.; Campbell, J.; Allen, L. E.; Gustincich, S.; Raymond, F. L.; Tartaglia, M.; Reid, Sheena Elisabeth Campbell
NPM1 mutational status underlines different biological features in pediatric AML
2021 Tregnago, C.; Benetton, M.; Padrin, D.; Polato, K.; Borella, G.; Da Ros, A.; Marchetti, A.; Porcu, E.; Del Bufalo, F.; Mecucci, C.; Locatelli, Franco; Pigazzi, M.
The Nrf2 Pathway in Depressive Disorders: A Systematic Review of Animal and Human Studies
2023 Sani, Gabriele; Margoni, Stella; Brugnami, Andrea; Ferrara, Ottavia Marianna; Bernardi, Evelina; Simonetti, Alessio; Monti, Laura; Mazza, Marianna; Janiri, Delfina; Moccia, Lorenzo; Kotzalidis, G. D.; Chieffo, Daniela Pia Rosaria; Janiri, Luigi
Nrf2-Mediated System xc- Activation in Astroglial Cells Is Involved in HIV-1 Tat-Induced Neurotoxicity
2019 Mastrantonio, Roberta; D'Ezio, Veronica; Colasanti, Marco; Persichini, Tiziana
Nuclear Expression of β-Catenin Is Associated with Improved Outcomes in Endometrial Cancer
2022 Masciullo, Valeria; Susini, Tommaso; Corrado, Giacomo; Stepanova, Marina; Baroni, Alessandro; Renda, Irene; Castiglione, Francesca; Minimo, Corrado; Bellacosa, Alfonso; Chiofalo, Benito; Vizza, Enrico; Scambia, Giovanni
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2000 | NOVEL MEMBERS OF THE PLEXIN FAMILY AND USES THEREOF | Artigiani, Stefania; COMOGLIO Paolo, M; GOODMAN Corey, S; TESSIER-LAVIGNE, Marc; Tamagnone, Luca | |
| 1-gen-2020 | A novel MEN1 pathogenic variant in an Italian patient with multiple endocrine neoplasia type 1 | Corsello, Andrea; Bruno, Carmine; Rizza, Roberta; Concolino, Paola; Papi, Giampaolo; Pontecorvi, Alfredo; Rindi, Guido; Paragliola, Rosa Maria | |
| 1-gen-2005 | A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer | Lucci-Cordisco, E; Zollino, Marcella; Baglioni, S; Mancuso, I; Lecce, R; Gurrieri, Fiorella; Crucitti, Antonio; Papi, L; Neri, G; Genuardi, Maurizio | |
| 1-gen-2019 | A novel nonsense PTH1R variant shows incomplete penetrance of primary failure of eruption: a case report | Grippaudo, Cristina; Cafiero, Concetta; D'Apolito, Isabella; Re, Agnese; Genuardi, Maurizio; Chiurazzi, Pietro; Frazier-Bowers, Sylvia A. | |
| 1-gen-2016 | Novel Osteointegrative Sr-Substituted Apatitic Cements Enriched with Alginate | Sprio, Simone; Dapporto, Massimiliano; Montesi, Monica; Panseri, Silvia; Lattanzi, Wanda; Pola, Enrico; Logroscino, Giandomenico; Tampieri, Anna | |
| 1-gen-2021 | A Novel Prognostic Marker for Primary CNS Lymphoma: Lactate Dehydrogenase-to-Lymphocyte Ratio Improves Stratification of Patients Within the Low and Intermediate MSKCC Risk Groups | Gao, Yuting; Wei, Li; Jin Kim, Seok; Wang, Liang; He, Yingzhi; Zheng, Yanfang; Bertero, Luca; Pellerino, Alessia; Cassoni, Paola; Tamagnone, Luca; Katharina Theresa, Prochazka; Deutsch, Alexander; Zhan, Huien; Lai, Jing; Wang, Yao; You, Hua | |
| 1-gen-2023 | A novel prognostic model based on pretreatment serum albumin and ECOG PS for primary CNS lymphoma: an international, multi-center study | Wei, Li; Gao, Yuting; Theresa Prochazka, Katharina; Liu, Rongqiu; Wang, Liang; Liu, Boyang; He, Yingzhi; Bertero, Luca; Pellerino Paola Cassoni, Alessia; Tamagnone, Luca; J Deutsch, Alexander; Zhan, Huien; Lai, Jing; Jin Kim, Seok; You, Hua | |
| 1-gen-2014 | A novel self-lipid antigen targets human T cells against CD1c(+) leukemias | Lepore, Marco; de Lalla, Claudia; Gundimeda, S Ramanjaneyulu; Gsellinger, Heiko; Consonni, Michela; Garavaglia, Claudio; Sansano, Sebastiano; Piccolo, Francesco; Scelfo, Andrea; Häussinger, Daniel; Montagna, Daniela; Locatelli, Franco; Bonini, Chiara; Bondanza, Attilio; Forcina, Alessandra; Li, Zhiyuan; Ni, Guanghui; Ciceri, Fabio; Jenö, Paul; Xia, Chengfeng; Mori, Lucia; Dellabona, Paolo; Casorati, Giulia; De Libero, Gennaro | |
| 1-gen-2022 | Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy | Bosco, Luca; Leone, Daniela; Costa Comellas, Laura; Monforte, Mauro; Pane, Marika; Mercuri, Eugenio Maria; Bertini, Enrico Silvio; D'Amico, Adele; Fattori, Fabiana | |
| 1-gen-2020 | Novel Therapeutic Approaches to Familial HLH (Emapalumab in FHL) | Merli, P.; Algeri, M.; Gaspari, S.; Locatelli, Franco | |
| 1-gen-2021 | Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis | Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, Amelia; Marangi, Giuseppe; Martello, Francesco; Bisogni, Giulia; Meleo, Emiliana; Colavito, Davide; Del Giudice, Elda; Patanella, Agata Katia; Bernardo, Daniela; Romano, Angela; Zollino, Marcella; Sabatelli, Mario | |
| 1-gen-2020 | De novo a-to-i rna editing discovery in lncrna | Silvestris, D. A.; Scopa, C.; Hanchi, S.; Locatelli, Franco; Gallo, A. | |
| 1-gen-2012 | De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. | Heinzen, El; Swoboda, Kj; Hitomi, Y; Gurrieri, Fiorella; Tiziano, Francesco Danilo; Nicole, S; Fontaine, B; De Vries, B; Walley, Nm; Heavin, S; Panagiotakaki, E; Koelewijn, S; Kamphorst, J; Geilenkirchen, M; Pelzer, N; Laan, L; Haan, J; Ferrari, Mirella; Van Den Maagdenberg, A; Fiori, S; Abiusi, Emanuela; Di Pietro, Lorena; Sweney, Mt; Newcomb, Tm; Viollet, L; Huff, C; Jorde, Lb; Reyna, Sp; Murphy, Kj; Shianna, Kv; Gumbs, Ce; Little, L; Silver, K; Ptáček, Lj; Haan, J; Herke, S Gk; Whitelaw, Cm; Webb, D; Lynch, Bj; Uldall, P; King, Md; Scheffer, Ie; Neri, Giovanni; Arzimanoglou, A; Sisodiya, Sm; Mikati, Ma; Goldstein, Db | |
| 1-gen-2021 | De novo partial 13q22-q34 trisomy with typical neurological and immunological findings: A case report with new genetic insights | Brogna, Claudia; Milano, Valentina; Brogna, B.; Cristiano, Lara; Rovere, Giuseppe; De Sanctis, Roberto; Romeo, Domenico Marco; Mercuri, Eugenio Maria; Zampino, Giuseppe | |
| 1-gen-2020 | De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides–Baraitser syndrome | Cappuccio, G.; Sayou, C.; Tanno, P. L.; Tisserant, E.; Bruel, A. -L.; Kennani, S. E.; Sa, J.; Low, K. J.; Dias, C.; Havlovicova, M.; Hancarova, M.; Eichler, E. E.; Devillard, F.; Moutton, S.; Van-Gils, J.; Dubourg, C.; Odent, S.; Gerard, B.; Piton, A.; Yamamoto, T.; Okamoto, N.; Firth, H.; Metcalfe, K.; Moh, A.; Chapman, K. A.; Aref-Eshghi, E.; Kerkhof, J.; Torella, A.; Nigro, V.; Perrin, L.; Piard, J.; Le Guyader, G.; Jouan, T.; Thauvin-Robinet, C.; Duffourd, Y.; George-Abraham, J. K.; Buchanan, C. A.; Williams, D.; Kini, U.; Wilson, K.; Nigro, V.; Brunetti-Pierri, N.; Casari, G.; Cappuccio, G.; Torella, A.; Pinelli, M.; Musacchia, F.; Mutarelli, M.; Carrella, D.; Vitiello, G.; Capra, V.; Parenti, G.; Leuzzi, V.; Selicorni, A.; Maitz, S.; Banfi, S.; Zollino, Marcella; Montomoli, M.; Milani, D.; Romano, C.; Tummolo, A.; De Brasi, D.; Coppola, A.; Santoro, C.; Peron, A.; Pantaleoni, C.; Castello, R.; D'Arrigo, S.; Sousa, S. B.; Hennekam, R. C. M.; Sadikovic, B.; Thevenon, J.; Govin, J.; Vitobello, A.; Brunetti-Pierri, N. | |
| 1-gen-2020 | De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment | Rodger, C.; Flex, E.; Allison, R. J.; Sanchis-Juan, A.; Hasenahuer, M. A.; Cecchetti, S.; French, C. E.; Edgar, J. R.; Carpentieri, G.; Ciolfi, A.; Pantaleoni, F.; Bruselles, A.; Onesimo, Roberta; Zampino, Giuseppe; Marcon, F.; Siniscalchi, E.; Lees, M.; Krishnakumar, D.; Mccann, E.; Yosifova, D.; Jarvis, J.; Kruer, M. C.; Marks, W.; Campbell, J.; Allen, L. E.; Gustincich, S.; Raymond, F. L.; Tartaglia, M.; Reid, Sheena Elisabeth Campbell | |
| 1-gen-2021 | NPM1 mutational status underlines different biological features in pediatric AML | Tregnago, C.; Benetton, M.; Padrin, D.; Polato, K.; Borella, G.; Da Ros, A.; Marchetti, A.; Porcu, E.; Del Bufalo, F.; Mecucci, C.; Locatelli, Franco; Pigazzi, M. | |
| 1-gen-2023 | The Nrf2 Pathway in Depressive Disorders: A Systematic Review of Animal and Human Studies | Sani, Gabriele; Margoni, Stella; Brugnami, Andrea; Ferrara, Ottavia Marianna; Bernardi, Evelina; Simonetti, Alessio; Monti, Laura; Mazza, Marianna; Janiri, Delfina; Moccia, Lorenzo; Kotzalidis, G. D.; Chieffo, Daniela Pia Rosaria; Janiri, Luigi | |
| 1-gen-2019 | Nrf2-Mediated System xc- Activation in Astroglial Cells Is Involved in HIV-1 Tat-Induced Neurotoxicity | Mastrantonio, Roberta; D'Ezio, Veronica; Colasanti, Marco; Persichini, Tiziana | |
| 1-gen-2022 | Nuclear Expression of β-Catenin Is Associated with Improved Outcomes in Endometrial Cancer | Masciullo, Valeria; Susini, Tommaso; Corrado, Giacomo; Stepanova, Marina; Baroni, Alessandro; Renda, Irene; Castiglione, Francesca; Minimo, Corrado; Bellacosa, Alfonso; Chiofalo, Benito; Vizza, Enrico; Scambia, Giovanni |
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