Generation of 3 human induced pluripotent stem cell lines LUMCi005-A, B and C from a Hereditary Cerebral Hemorrhage with Amyloidosis-Dutch type patient

Hereditary Cerebral Hemorrhage with Amyloidosis-Dutch type (HCHWA-D) is an autosomal dominant hereditary disease caused by a point mutation in exon 17 of the APP gene. We generated human induced pluripotent stem cells (hiPSCs) from a symptomatic HCHWA-D patient by using non-integrating Sendai virus (SeV). The newly generated hiPSCs express all pluripotency markers, have a normal karyotype, carry the Dutch mutation, can differentiate in the three germ layers in vitro and are SeV free.

Verfasser: Daoutsali, E. (Elena)
Buijsen, R.A.M. (Ronald)
Pas, S. (Simone) van de
Jong, A. (Anke 't)
Mikkers, H. (H.)
Brands, T. (Tom)
Eussen, H.J.F.M.M. (Bert)
Klein, A. (Annelies) de
van der Graaf, L.M. (Linda M.)
Pepers, B.A. (Barry)
Freund, C. (Christian)
Terwindt, G.M. (Gisela)
Orlova, V.V. (Valeria V.)
Roon-Mom, W.M.C. (Willeke) van
Dokumenttyp: Artikel
Erscheinungsdatum: 2019
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29035168
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://repub.eur.nl/pub/113801