Sfoglia per SSD
Sae2 and Rif2 regulate MRX endonuclease activity at DNA double-strand breaks in opposite manners
2021 Marsella, A; Gobbini, E; Cassani, C; Tisi, R; Cannavo, E; Reginato, G; Cejka, P; Longhese, M
Interplay between Sae2 and Rif2 in the regulation of Mre11-Rad50 activities at DNA ends
2021 Bonetti, D; Clerici, M; Longhese, M
Lactic acid-based deep eutectic solvents for the extraction of bioactive metabolites of Humulus lupulus L.: supramolecular organization, phytochemical profiling and biological activity
2021 Macchioni, V; Carbone, K; Cataldo, A; Fraschini, R; Bellucci, S
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
2021 Walsh, R; Lahrouchi, N; Tadros, R; Kyndt, F; Glinge, C; Postema, P; Amin, A; Nannenberg, E; Ware, J; Whiffin, N; Mazzarotto, F; Skoric-Milosavljevic, D; Krijger, C; Arbelo, E; Babuty, D; Barajas-Martinez, H; Beckmann, B; Bezieau, S; Bos, J; Breckpot, J; Campuzano, O; Castelletti, S; Celen, C; Clauss, S; Corveleyn, A; Crotti, L; Dagradi, F; de Asmundis, C; Denjoy, I; Dittmann, S; Ellinor, P; Ortuno, C; Giustetto, C; Gourraud, J; Hazeki, D; Horie, M; Ishikawa, T; Itoh, H; Kaneko, Y; Kanters, J; Kimoto, H; Kotta, M; Krapels, I; Kurabayashi, M; Lazarte, J; Leenhardt, A; Loeys, B; Lundin, C; Makiyama, T; Mansourati, J; Martins, R; Mazzanti, A; Morner, S; Napolitano, C; Ohkubo, K; Papadakis, M; Rudic, B; Molina, M; Sacher, F; Sahin, H; Sarquella-Brugada, G; Sebastiano, R; Sharma, S; Sheppard, M; Shimamoto, K; Shoemaker, M; Stallmeyer, B; Steinfurt, J; Tanaka, Y; Tester, D; Usuda, K; van der Zwaag, P; Van Dooren, S; Van Laer, L; Winbo, A; Winkel, B; Yamagata, K; Zumhagen, S; Volders, P; Lubitz, S; Antzelevitch, C; Platonov, P; Odening, K; Roden, D; Roberts, J; Skinner, J; Tfelt-Hansen, J; van den Berg, M; Olesen, M; Lambiase, P; Borggrefe, M; Hayashi, K; Rydberg, A; Nakajima, T; Yoshinaga, M; Saenen, J; Kaab, S; Brugada, P; Robyns, T; Giachino, D; Ackerman, M; Brugada, R; Brugada, J; Gimeno, J; Hasdemir, C; Guicheney, P; Priori, S; Schulze-Bahr, E; Makita, N; Schwartz, P; Shimizu, W; Aiba, T; Schott, J; Redon, R; Ohno, S; Probst, V; Arnaout, A; Amelot, M; Anselme, F; Billon, O; Defaye, P; Dupuis, J; Jesel, L; Laurent, G; Maury, P; Pasquie, J; Wiart, F; Behr, E; Barc, J; Bezzina, C
Role of the Sox2 and COUP-TF1 transcription factors in the development of the visual system by conditional knock-out in mouse
2020 Serra, L
Progenitor Cell Differentiation As a Gradient Flow
2020 Crosta, G
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition
2020 Roberts, J; Asaki, S; Mazzanti, A; Bos, J; Tuleta, I; Muir, A; Crotti, L; Krahn, A; Kutyifa, V; Shoemaker, M; Johnsrude, C; Aiba, T; Marcondes, L; Baban, A; Udupa, S; Dechert, B; Fischbach, P; Knight, L; Vittinghoff, E; Kukavica, D; Stallmeyer, B; Giudicessi, J; Spazzolini, C; Shimamoto, K; Tadros, R; Cadrin-Tourigny, J; Duff, H; Simpson, C; Roston, T; Wijeyeratne, Y; El Hajjaji, I; Yousif, M; Gula, L; Leong-Sit, P; Chavali, N; Landstrom, A; Marcus, G; Dittmann, S; Wilde, A; Behr, E; Tfelt-Hansen, J; Scheinman, M; Perez, M; Kaski, J; Gow, R; Drago, F; Aziz, P; Abrams, D; Gollob, M; Skinner, J; Shimizu, W; Kaufman, E; Roden, D; Zareba, W; Schwartz, P; Schulze-Bahr, E; Etheridge, S; Priori, S; Ackerman, M
Cytokinesis in Eukaryotic Cells: The Furrow Complexity at a Glance
2020 Fraschini, R
Functional and structural insights into the MRX/MRN complex, a key player in recognition and repair of DNA double-strand breaks
2020 Tisi, R; Vertemara, J; Zampella, G; Longhese, M
A novel coordinated function of Myosin II with GOLPH3 controls centralspindlin localization during cytokinesis in Drosophila
2020 Sechi, S; Frappaolo, A; Karimpour-Ghahnavieh, A; Fraschini, R; Giansanti, M
DNA binding modes influence Rap1 activity in the regulation of telomere length and MRX functions at DNA ends
2020 Bonetti, D; Rinaldi, C; Vertemara, J; Notaro, M; Pizzul, P; Tisi, R; Zampella, G; Longhese, M
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome
2020 Lahrouchi, N; Tadros, R; Crotti, L; Mizusawa, Y; Postema, P; Beekman, L; Walsh, R; Hasegawa, K; Barc, J; Ernsting, M; Turkowski, K; Mazzanti, A; Beckmann, B; Shimamoto, K; Diamant, U; Wijeyeratne, Y; Kucho, Y; Robyns, T; Ishikawa, T; Arbelo, E; Christiansen, M; Winbo, A; Jabbari, R; Lubitz, S; Steinfurt, J; Rudic, B; Loeys, B; Shoemaker, M; Weeke, P; Pfeiffer, R; Davies, B; Andorin, A; Hofman, N; Dagradi, F; Pedrazzini, M; Tester, D; Bos, J; Sarquella-Brugada, G; Campuzano, Ó; Platonov, P; Stallmeyer, B; Zumhagen, S; Nannenberg, E; Veldink, J; van den Berg, L; Al-Chalabi, A; Shaw, C; Shaw, P; Morrison, K; Andersen, P; Müller-Nurasyid, M; Cusi, D; Barlassina, C; Galan, P; Lathrop, M; Munter, M; Werge, T; Ribasés, M; Aung, T; Khor, C; Ozaki, M; Lichtner, P; Meitinger, T; van Tintelen, J; Hoedemaekers, Y; Denjoy, I; Leenhardt, A; Napolitano, C; Shimizu, W; Schott, J; Gourraud, J; Makiyama, T; Ohno, S; Itoh, H; Krahn, A; Antzelevitch, C; Roden, D; Saenen, J; Borggrefe, M; Odening, K; Ellinor, P; Tfelt-Hansen, J; Skinner, J; van den Berg, M; Olesen, M; Brugada, J; Brugada, R; Makita, N; Breckpot, J; Yoshinaga, M; Behr, E; Rydberg, A; Aiba, T; Kääb, S; Priori, S; Guicheney, P; Tan, H; Newton-Cheh, C; Ackerman, M; Schwartz, P; Schulze-Bahr, E; Probst, V; Horie, M; Wilde, A; Tanck, M; Bezzina, C
SCN5A mutation type and a genetic risk score associate variably with brugada syndrome phenotype in SCN5A families
2020 Wijeyeratne, Y; Tanck, M; Mizusawa, Y; Batchvarov, V; Barc, J; Crotti, L; Bos, J; Tester, D; Muir, A; Veltmann, C; Ohno, S; Page, S; Galvin, J; Tadros, R; Muggenthaler, M; Raju, H; Denjoy, I; Schott, J; Gourraud, J; Skoric-Milosavljevic, D; Nannenberg, E; Redon, R; Papadakis, M; Kyndt, F; Dagradi, F; Castelletti, S; Torchio, M; Meitinger, T; Lichtner, P; Ishikawa, T; Wilde, A; Takahashi, K; Sharma, S; Roden, D; Borggrefe, M; Mckeown, P; Shimizu, W; Horie, M; Makita, N; Aiba, T; Ackerman, M; Schwartz, P; Probst, V; Bezzina, C; Behr, E
Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk
2020 Musa, H; Marcou, C; Herron, T; Makara, M; Tester, D; O'Connell, R; Rosinski, B; Guerrero-Serna, G; Milstein, M; Monteiro Da Rocha, A; Ye, D; Crotti, L; Nesterenko, V; Castelletti, S; Torchio, M; Kotta, M; Dagradi, F; Antzelevitch, C; Mohler, P; Schwartz, P; Ackerman, M; Anumonwo, J
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1
2020 Mura, M; Bastaroli, F; Corli, M; Ginevrino, M; Calabrò, F; Boni, M; Crotti, L; Valente, E; Schwartz, P; Gnecchi, M
How do cells sense DNA lesions?
2020 Colombo, C; Gnugnoli, M; Gobbini, E; Longhese, M
Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome
2020 Dagradi, F; Spazzolini, C; Castelletti, S; Pedrazzini, M; Kotta, M; Crotti, L; Schwartz, P
New insights into the regulation of DNA end processing and DNA damage checkpoint
2019 Colombo, C
Role of Tel1/ATM in protecting and signaling abnormal replication forks and short telomeres
2019 Menin, L
Spindle pole power in health and disease
2019 Raspelli, E; Fraschini, R
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