Sfoglia per SSD
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation
2019 Mura, M; Lee, Y; Pisano, F; Ginevrino, M; Boni, M; Calabrò, F; Crotti, L; Valente, E; Schwartz, P; Tse, H; Gnecchi, M
Uncoupling Sae2 functions in downregulation of Tel1 and Rad53 signaling activities
2019 Colombo, C; Menin, L; Ranieri, R; Bonetti, D; Clerici, M; Longhese, M
Editorial: Model Organisms: A Precious Resource for the Understanding of Molecular Mechanisms Underlying Human Physiology and Disease
2019 Fraschini, R; Giansanti, M
Spindle pole power in health and disease
2019 Raspelli, E; Fraschini, R
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population
2019 Mura, M; Pisano, F; Stefanello, M; Ginevrino, M; Boni, M; Calabrò, F; Crotti, L; Valente, E; Schwartz, P; Brink, P; Gnecchi, M
Processing of DNA double-strand breaks by the MRX complex in a chromatin context
2019 Casari, E; Rinaldi, C; Marsella, A; Gnugnoli, M; Colombo, C; Bonetti, D; Longhese, M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene
2019 Mura, M; Pisano, F; Stefanello, M; Ginevrino, M; Boni, M; Calabrò, F; Crotti, L; Valente, E; Schwartz, P; Brink, P; Gnecchi, M
Divide Precisely and Proliferate Safely: Lessons from Budding Yeast
2019 Fraschini, R
Genetic Mosaicism in Calmodulinopathy
2019 Wren, L; Jiménez-Jáimez, J; Al-Ghamdi, S; Al-Aama, J; Bdeir, A; Al-Hassnan, Z; Kuan, J; Foo, R; Potet, F; Johnson, C; Aziz, M; Carvill, G; Kaski, J; Crotti, L; Perin, F; Monserrat, L; Burridge, P; Schwartz, P; Chazin, W; Bhuiyan, Z; George AL, J
Structure–function relationships of the Mre11 protein in the control of DNA end bridging and processing
2019 Marsella, A; Cassani, C; Casari, E; Tisi, R; Longhese, M
International Triadin Knockout Syndrome Registry: The Clinical Phenotype and Treatment Outcomes of Patients with Triadin Knockout Syndrome
2019 Clemens, D; Tester, D; Giudicessi, J; Bos, J; Rohatgi, R; Abrams, D; Balaji, S; Crotti, L; Faure, J; Napolitano, C; Priori, S; Probst, V; Rooryck-Thambo, C; Roux-Buisson, N; Sacher, F; Schwartz, P; Silka, M; Walsh, M; Ackerman, M
Regulation of DNA-end resection at DNA double strand breaks and stalled replication forks
2018 Villa, M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene
2018 Mura, M; Lee, Y; Ginevrino, M; Zappatore, R; Pisano, F; Boni, M; Dagradi, F; Crotti, L; Valente, E; Schwartz, P; Tse, H; Gnecchi, M
Genetica dello sviluppo animale
2018 Nicolis, S
Sox2 functions in neural cancer stem cells: the importance of the context
2018 Barone, C; Pagin, M; Serra, L; Motta, A; Rigoldi, L; Giubbolini, S; Badiola-Sanga, A; Mercurio, S; Nicolis, S
Risk stratification for sudden cardiac death in primary electrical disorders.
2018 Schwartz, P; Crotti, L
Monogenic and oligogenic cardiovascular diseases: genetics of arrhythmias—Catecholaminergic polymorphic ventricular tachycardia.
2018 Schwartz, P; Crotti, L
Modifier genes for sudden cardiac death.
2018 Schwartz, P; Crotti, L; George, A
The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?
2018 Leinonen, J; Crotti, L; Djupsjöbacka, A; Castelletti, S; Junna, N; Ghidoni, A; Tuiskula, A; Spazzolini, C; Dagradi, F; Viitasalo, M; Kontula, K; Kotta, M; Widén, E; Swan, H; Schwartz, P
R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome
2018 Catania, A; Battini, R; Pippucci, T; Pasquariello, R; Chiapparini, M; Seri, M; Garavaglia, B; Zorzi, G; Nardocci, N; Ghezzi, D; Tiranti, V
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