Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Schwartz, Peter J  [Clear All Filters]
2019
Schwartz, P.J., Gnecchi, M., Dagradi, F., Castelletti, S., Parati, G., Spazzolini, C., Sala, L., and Crotti, L. (2019). From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2.Eur Heart J.
Mura, M., Lee, Y.-K., Pisano, F., Ginevrino, M., Boni, M., Calabrò, F., Crotti, L., Valente, E.Maria, Schwartz, P.J., Tse, H.-F., et al. (2019). Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation.Stem Cell Res37, 101431.
Mura, M., Lee, Y.-K., Pisano, F., Ginevrino, M., Boni, M., Calabrò, F., Crotti, L., Valente, E.Maria, Schwartz, P.J., Tse, H.-F., et al. (2019). Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation.Stem Cell Res37, 101437.
Mura, M., Pisano, F., Stefanello, M., Ginevrino, M., Boni, M., Calabrò, F., Crotti, L., Valente, E.Maria, Schwartz, P.J., Brink, P.A., et al. (2019). 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.Stem Cell Res36, 101416.
Mura, M., Pisano, F., Stefanello, M., Ginevrino, M., Boni, M., Calabrò, F., Crotti, L., Valente, E.Maria, Schwartz, P.J., Brink, P.A., et al. (2019). Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population.Stem Cell Res39, 101510.
Wren, L.M., Jiménez-Jáimez, J., Al-Ghamdi, S., Al-Aama, J.Y., Bdeir, A., Al-Hassnan, Z.N., Kuan, J.L., Foo, R.Y., Potet, F., Johnson, C.N., et al. (2019). Genetic Mosaicism in Calmodulinopathy.Circ Genom Precis Med.
Wu, J.C., Garg, P., Yoshida, Y., Yamanaka, S., Gepstein, L., Hulot, J.-S., Knollmann, B.C., and Schwartz, P.J. (2019). Towards Precision Medicine With Human iPSCs for Cardiac Channelopathies.Circ Res125, 653-658.