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Amandine Caillaud

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Bioengineering & Translational Medicine|July 22, 2024
Human induced pluripotent stem cells-derived liver organoids grown on a Biomimesys® hyaluronic acid-based hydroscaffold as a new model for studying human lipoprotein metabolismMeryl Roudaut, Amandine Caillaud, Zied Souguir, et al.
International Journal of Molecular Sciences|April 23, 2022
<i>APOB</i> CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel VariantsXavier Vanhoye, Alexandre Janin, Amandine Caillaud, et al.
STAR Protocols|September 17, 2022
FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cellsAmandine Caillaud, Antoine Lévêque, Aurélie Thédrez, et al.
Stem Cell Reports|November 5, 2021
PCSK9 regulates the NODAL signaling pathway and cellular proliferation in hiPSCsMeryl Roudaut, Salam Idriss, Amandine Caillaud, et al.
Stem Cell Research|January 9, 2022
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic backgroundAurore Girardeau, Diane Atticus, Robin Canac, et al.
European Journal of Human Genetics : EJHG|February 19, 2020
A dominant vimentin variant causes a rare syndrome with premature agingBenjamin Cogné, Jamal-Eddine Bouameur, Gaëlle Hayot, et al.
Circulation|July 28, 2022
Identification of a Gain-of-Function <i>LIPC</i> Variant as a Novel Cause of Familial Combined HypocholesterolemiaWieneke Dijk, Mathilde Di Filippo, Sander Kooijman, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 1, 2022
Variants in the <i>GPR146</i> Gene Are Associated With a Favorable Cardiometabolic Risk ProfileAntoine Rimbert, Ming W Yeung, Nawar Dalila, et al.
Haematologica|June 15, 2023
Characterization of genetic variants in the <i>EGLN1/PHD2</i> gene identified in a European collection of patients with erythrocytosisMarine Delamare, Amandine Le Roy, Mathilde Pacault, et al.
The New England Journal of Medicine|April 30, 2025
Identification of Hepatic-like EPO as a Cause of PolycythemiaLaurent Martin, Darko Maric, Salam Idriss, et al.
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Showing results (11-20 of 20) with videos related to

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You have reached the last page of results.This site can display upto 20 results.
Bioengineering & Translational Medicine|July 22, 2024
Human induced pluripotent stem cells-derived liver organoids grown on a Biomimesys® hyaluronic acid-based hydroscaffold as a new model for studying human lipoprotein metabolismMeryl Roudaut, Amandine Caillaud, Zied Souguir, et al.
International Journal of Molecular Sciences|April 23, 2022
<i>APOB</i> CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel VariantsXavier Vanhoye, Alexandre Janin, Amandine Caillaud, et al.
STAR Protocols|September 17, 2022
FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cellsAmandine Caillaud, Antoine Lévêque, Aurélie Thédrez, et al.
Stem Cell Reports|November 5, 2021
PCSK9 regulates the NODAL signaling pathway and cellular proliferation in hiPSCsMeryl Roudaut, Salam Idriss, Amandine Caillaud, et al.
Stem Cell Research|January 9, 2022
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic backgroundAurore Girardeau, Diane Atticus, Robin Canac, et al.
European Journal of Human Genetics : EJHG|February 19, 2020
A dominant vimentin variant causes a rare syndrome with premature agingBenjamin Cogné, Jamal-Eddine Bouameur, Gaëlle Hayot, et al.
Circulation|July 28, 2022
Identification of a Gain-of-Function <i>LIPC</i> Variant as a Novel Cause of Familial Combined HypocholesterolemiaWieneke Dijk, Mathilde Di Filippo, Sander Kooijman, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 1, 2022
Variants in the <i>GPR146</i> Gene Are Associated With a Favorable Cardiometabolic Risk ProfileAntoine Rimbert, Ming W Yeung, Nawar Dalila, et al.
Haematologica|June 15, 2023
Characterization of genetic variants in the <i>EGLN1/PHD2</i> gene identified in a European collection of patients with erythrocytosisMarine Delamare, Amandine Le Roy, Mathilde Pacault, et al.
The New England Journal of Medicine|April 30, 2025
Identification of Hepatic-like EPO as a Cause of PolycythemiaLaurent Martin, Darko Maric, Salam Idriss, et al.
Pageof 2