Sfoglia per SSD
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
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-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-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. |
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