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The NIPBL-gene mutation of a Cornelia de Lange Syndrome patient causes deficits in the hepatocyte differentiation of induced Pluripotent Stem Cells via altered chromatin-accessibility

Title:	The NIPBL-gene mutation of a Cornelia de Lange Syndrome patient causes deficits in the hepatocyte differentiation of induced Pluripotent Stem Cells via altered chromatin-accessibility
Authors:	Foglia, Marika^Aff1; Guarrera, Luca^Aff1; Kurosaki, Mami^Aff1; Cassanmagnago, Giada Andrea^Aff2; Bolis, Marco^{Aff2, Aff3}; Miduri, Matteo^Aff1; Cereseto, Anna^Aff4; Umbach, Alessandro^Aff4; Craparotta, Ilaria^Aff2; Fratelli, Maddalena^Aff1; Vallerga, Arianna^Aff1; Paroni, Gabriela^Aff1; Zanetti, Adriana^Aff1; Cavallaro, Andrea Vincenzo^Aff1; Russo, Luca^Aff5; Garattini, Enrico^Aff1; Terao, Mineko^{Aff1, IDs0001802405481z_cor17}
Source:	Cellular and Molecular Life Sciences. 81(1)
Database:	Springer Nature Journals