Sfoglia per SSD
Genetica dello sviluppo animale
2018 Nicolis, S
Snf1/AMPK is involved in the mitotic spindle alignment in Saccharomyces cerevisiae
2018 Tripodi, F; Fraschini, R; Zocchi, M; Reghellin, V; Coccetti, P
Swe1 and Mih1 regulate mitotic spindle dynamics in budding yeast via Bik1
2018 Raspelli, E; Facchinetti, S; Fraschini, R
Modifier genes for sudden cardiac death.
2018 Schwartz, P; Crotti, L; George, A
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
2018 Baruteau, A; Kyndt, F; Behr, E; Vink, A; Lachaud, M; Joong, A; Schott, J; Horie, M; Denjoy, I; Crotti, L; Shimizu, W; Bos, J; Stephenson, E; Wong, L; Abrams, D; Davis, A; Winbo, A; Dubin, A; Sanatani, S; Liberman, L; Kaski, J; Rudic, B; Kwok, S; Rieubland, C; Tfelt-Hansen, J; Van Hare, G; Guyomarc'h-Delasalle, B; Blom, N; Wijeyeratne, Y; Gourraud, J; Le Marec, H; Ozawa, J; Fressart, V; Lupoglazoff, J; Dagradi, F; Spazzolini, C; Aiba, T; Tester, D; Zahavich, L; Beauséjour-Ladouceur, V; Jadhav, M; Skinner, J; Franciosi, S; Krahn, A; Abdelsayed, M; Ruben, P; Yung, T; Ackerman, M; Wilde, A; Schwartz, P; Probst, V
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
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
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
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1
2018 Mura, M; Ginevrino, M; Zappatore, R; Pisano, F; Boni, M; Castelletti, S; Crotti, L; Valente, E; Schwartz, P; Gnecchi, M
Rad9/53BP1 protects stalled replication forks from degradation in Mec1/ATR-defective cells
2018 Villa, M; Bonetti, D; Carraro, M; Longhese, M
Risk stratification for sudden cardiac death in primary electrical disorders.
2018 Schwartz, P; Crotti, L
Factors that control mitotic spindle dynamics
2017 Fraschini, R
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H2O2-induced oxidative stress and cytotoxicity in vitro
2017 Chisci, E; De Giorgi, M; Zanfrini, E; Testasecca, A; Brambilla, E; Cinti, A; Farina, L; Kutryb Zając, B; Bugarin, C; Villa, C; Grassilli, E; Combi, R; Gaipa, G; Cerrito, M; Rivolta, I; Smolenski, R; Lavitrano, M; Giovannoni, R
Fluorescence microscopy applied to the analysis of mitotic spindle dynamics
2017 Fraschini, R
The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by Long QT Syndrome type 2
2017 Mura, M; Mehta, A; Ramachandra, C; Zappatore, R; Pisano, F; Ciuffreda, M; Barbaccia, V; Crotti, L; Schwartz, P; Shim, W; Gnecchi, M
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation
2017 Castelletti, S; Vischer, A; Syrris, P; Crotti, L; Spazzolini, C; Ghidoni, A; Parati, G; Jenkins, S; Kotta, M; Mckenna, W; Schwartz, P; Pantazis, A
Evolutionary restoration of fertility in an interspecies hybrid yeast, by whole-genome duplication after a failed mating-type switch
2017 Ortiz-merino, R; Kuanyshev, N; Braun-galleani, S; Byrne, K; Porro, D; Branduardi, P; Wolfe, K
Rab1 interacts with GOLPH3 and controls Golgi structure and contractile ring constriction during cytokinesis in Drosophila melanogaster.
2017 Sechi, S; Frappaolo, A; Fraschini, R; Capalbo, L; Gottardo, M; Belloni, G; Glover, D; Wainman, A; Giansanti, M
COG7 deficiency in Drosophila generates multifaceted developmental, behavioral and protein glycosylation phenotypes
2017 Frappaolo, A; Sechi, S; Kumagai, T; Robinson, S; Fraschini, R; Ghahnavieh, A; Belloni, G; Piergentili, R; Tiemeyer, K; Tiemeyer, M; Giansanti, M
The role of genetics in primary ventricular fibrillation, inherited channelopathies and cardiomyopathies
2017 Crotti, L; Kotta, M
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