Sfoglia per SSD
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
Sox2-Dependent 3D Chromatin Interactomes in Transcription, Neural Stem Cell Proliferation and Neurodevelopmental Diseases
2019 Wei, C; Nicolis, S; Zhu, Y; Pagin, M
Genetic of adult and fetal forms of Long QT Syndrome.
2019 Crotti, L; Ghidoni, A; Dagradi, F
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
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
The pleiotropic effects of GATA1 and KLF1 in physiological erythropoiesis and in dyserythropoietic disorders
2019 Barbarani, G; Fugazza, C; Strouboulis, J; Ronchi, A
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
Spindle pole power in health and disease
2019 Raspelli, E; Fraschini, R
Divide Precisely and Proliferate Safely: Lessons from Budding Yeast
2019 Fraschini, R
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
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
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation
2019 Mura, M; Lee, Y; Pisano, F; Ginevrino, M; Boni, M; Calabrò, F; Crotti, L; Valente, E; Schwartz, P; Tse, H; 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
Regulation of DNA-end resection at DNA double strand breaks and stalled replication forks
2018 Villa, M
Monogenic and oligogenic cardiovascular diseases: genetics of arrhythmias—Catecholaminergic polymorphic ventricular tachycardia.
2018 Schwartz, P; Crotti, L
Local unwinding of double-strand DNA ends by the MRX complex promotes Exo1 processing activity
2018 Gobbini, E; Vertemara, J; Longhese, M
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
Genetica dello sviluppo animale
2018 Nicolis, S
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