Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Girardeau, Aurore  [Clear All Filters]
2024
Geryk M, Canac R, Forest V, Lindenbaum P, Girardeau A, Baudic M, Baron E, Bibonne A, Chariau C, Kyndt F, et al. Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in line. Stem Cell Res. 2024;77:103396.
2023
Caillaud A, Bray L, Girardeau A, Begué-Racapé Z, Vince L, Patitucci M, Le May C, Lambert G, Cariou B, Rimbert A. Generation of an induced pluripotent stem cell line (ITXi012-A) from a patient with genetically determined high-lipoprotein(a) plasma levels. Stem Cell Res. 2023;72:103205.
2022
Bray L, Caillaud A, Girardeau A, Patitucci M, Le May C, Cariou B, Rimbert A. Generation of a GPR146 knockout human induced pluripotent stem cell line (ITXi001-A-1). Stem Cell Res. 2022;60:102721.
2021
Sayed ZRAl, Jouni M, Gourraud J-B, Belbachir N, Barc J, Girardeau A, Forest V, Derevier A, Gaignerie A, Chariau C, et al. A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype. Clin Transl Med. 2021;11(6):e413.
Cimarosti B, Canac R, Girardeau A, Arnaud M, Francheteau Q, Probst V, Lemarchand P, Redon R, Gourraud J-B, Gaborit N, et al. Generation of human induced pluripotent stem cell lines from two patients affected by catecholamine-induced QT prolongation (CIQTP). Stem Cell Res. 2021;59:102649.
Canac R, Caillaud A, Cimarosti B, Girardeau A, Hamamy H, Reversade B, Bonnard C, Sayed ZRAl, David L, Poschmann J, et al. Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system. Stem Cell Res. 2021;58:102627.
Roudaut M, Idriss S, Caillaud A, Girardeau A, Rimbert A, Champon B, David A, Lévêque A, Arnaud L, Pichelin M, et al. PCSK9 regulates the NODAL signaling pathway and cellular proliferation in hiPSCs. Stem Cell Reports. 2021.
2020
Sayed ZRAl, Canac R, Cimarosti B, Bonnard C, Gourraud J-B, Hamamy H, Kayserili H, Girardeau A, Jouni M, Jacob N, et al. Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction. Cardiovasc Res. 2020.