Sfoglia per SSD
Phosphoryl-EZH-ion
2011 Caretti, G.; Palacios, Daniela; Sartorelli, V.; Puri, P. L.
Praja1 E3 ubiquitin ligase promotes skeletal myogenesis through degradation of EZH2 upon p38α activation
2017 Consalvi, S.; Brancaccio, A.; Dall'Agnese, A.; Puri, P. L.; Palacios, Daniela
Rare Pathogenic Variants Predispose to Hepatocellular Carcinoma in Nonalcoholic Fatty Liver Disease
2019 Pelusi, Serena; Baselli, Guido; Pietrelli, Alessandro; Dongiovanni, Paola; Donati, Maria Benedetta; Mccain, Misti Vanette; Meroni, Marica; Fracanzani, Anna Ludovica; Romagnoli, Renato; Petta, Salvatore; Grieco, Antonio; Miele, Luca; Soardo, Giorgio; Bugianesi, Elisabetta; Fargion, Silvia; Aghemo, Alessio; D'Ambrosio, Roberta; Xing, Chao; Romeo, Stefano; De Francesco, Raffaele; Reeves, Helen Louise; Valenti, Luca Vittorio Carlo
Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration.
2009 Colombo, Roberto; Tavian, Daniela; Baker, Matthew; Richardson, Anna; Snowden, Julie; Neary, David; Mann, David; Pickering Brown, Stuart
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).
2025 Hendricks, Laj; Verbeek, Kcj; Schuurs-Hoeijmakers, Jhm; De Jong, Mm; Links, Tp; Brems, H; Aerden, M; Brunet, J; Lleuger-Pujol, R; Hüneburg, R; Aretz, S; Colas, C; Villy, Mc; Woodward, Er; Evans, Dg; Bosch, Dgm; Donze, Sh; Foretová, L; Blatnik, A; Leter, Em; Tischkowitz, M; Jahn, A; De Putter, R; Dupont, J; Briskemyr, S; Steinke-Lange, V; Baldassarri, M; Anastasiadou, Vc; Irmejs, A; Oliveira, C; Van Der Post, Rs; Mensenkamp, Ar; Tesi, B; Mu, N; Benusiglio, Pr; Gerasimenko, A; Innella, G; Turchetti, D; Houdayer, C; Branchaud, M; Høberg Vetti, H; Tveit Haavind, M; Balmaña, J; Torres, M; Genuardi, Maurizio; Panfili, A; Jørgensen, K; Mæhle, L; Hoogerbrugge, N; Vos, Jr.
SNeP: A tool to estimate trends in recent effective population size trajectories using genome-wide SNP data
2015 Barbato, Mario; Orozco-terWengel, Pablo; Tapio, Miika; Bruford, Michael W.
Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1
2012 Zhou, J; Tawk, M; Tiziano, Francesco Danilo; Veillet, J; Bayes, M; Nolent, F; Garcia, V; Servidei, Serenella; Bertini, E; Castro Giner, F; Renda, Y; Carpentier, S; Andrieu Abadie, N; Gut, I; Levade, T; Topaloglu, H; Melki, J.
Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD
2015 Lattante, Serena; De Calbiac, H; Le Ber, I; Brice, A; Ciura, S; Kabashi, E.
TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration
2010 Palacios, Daniela; Mozzetta, C.; Consalvi, S.; Caretti, G.; Saccone, Valentina; Proserpio, V.; Marquez, V. E.; Valente, S.; Mai, A.; Forcales, S. V.; Sartorelli, V.; Puri, P. L.
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2011 | Phosphoryl-EZH-ion | Caretti, G.; Palacios, Daniela; Sartorelli, V.; Puri, P. L. | |
| 1-gen-2017 | Praja1 E3 ubiquitin ligase promotes skeletal myogenesis through degradation of EZH2 upon p38α activation | Consalvi, S.; Brancaccio, A.; Dall'Agnese, A.; Puri, P. L.; Palacios, Daniela | |
| 1-gen-2019 | Rare Pathogenic Variants Predispose to Hepatocellular Carcinoma in Nonalcoholic Fatty Liver Disease | Pelusi, Serena; Baselli, Guido; Pietrelli, Alessandro; Dongiovanni, Paola; Donati, Maria Benedetta; Mccain, Misti Vanette; Meroni, Marica; Fracanzani, Anna Ludovica; Romagnoli, Renato; Petta, Salvatore; Grieco, Antonio; Miele, Luca; Soardo, Giorgio; Bugianesi, Elisabetta; Fargion, Silvia; Aghemo, Alessio; D'Ambrosio, Roberta; Xing, Chao; Romeo, Stefano; De Francesco, Raffaele; Reeves, Helen Louise; Valenti, Luca Vittorio Carlo | |
| 1-gen-2009 | Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration. | Colombo, Roberto; Tavian, Daniela; Baker, Matthew; Richardson, Anna; Snowden, Julie; Neary, David; Mann, David; Pickering Brown, Stuart | |
| 1-gen-2025 | The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS). | Hendricks, Laj; Verbeek, Kcj; Schuurs-Hoeijmakers, Jhm; De Jong, Mm; Links, Tp; Brems, H; Aerden, M; Brunet, J; Lleuger-Pujol, R; Hüneburg, R; Aretz, S; Colas, C; Villy, Mc; Woodward, Er; Evans, Dg; Bosch, Dgm; Donze, Sh; Foretová, L; Blatnik, A; Leter, Em; Tischkowitz, M; Jahn, A; De Putter, R; Dupont, J; Briskemyr, S; Steinke-Lange, V; Baldassarri, M; Anastasiadou, Vc; Irmejs, A; Oliveira, C; Van Der Post, Rs; Mensenkamp, Ar; Tesi, B; Mu, N; Benusiglio, Pr; Gerasimenko, A; Innella, G; Turchetti, D; Houdayer, C; Branchaud, M; Høberg Vetti, H; Tveit Haavind, M; Balmaña, J; Torres, M; Genuardi, Maurizio; Panfili, A; Jørgensen, K; Mæhle, L; Hoogerbrugge, N; Vos, Jr. | |
| 1-gen-2015 | SNeP: A tool to estimate trends in recent effective population size trajectories using genome-wide SNP data | Barbato, Mario; Orozco-terWengel, Pablo; Tapio, Miika; Bruford, Michael W. | |
| 1-gen-2012 | Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 | Zhou, J; Tawk, M; Tiziano, Francesco Danilo; Veillet, J; Bayes, M; Nolent, F; Garcia, V; Servidei, Serenella; Bertini, E; Castro Giner, F; Renda, Y; Carpentier, S; Andrieu Abadie, N; Gut, I; Levade, T; Topaloglu, H; Melki, J. | |
| 1-gen-2015 | Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD | Lattante, Serena; De Calbiac, H; Le Ber, I; Brice, A; Ciura, S; Kabashi, E. | |
| 1-gen-2010 | TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration | Palacios, Daniela; Mozzetta, C.; Consalvi, S.; Caretti, G.; Saccone, Valentina; Proserpio, V.; Marquez, V. E.; Valente, S.; Mai, A.; Forcales, S. V.; Sartorelli, V.; Puri, P. L. |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile