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Camille Humbert

Showing results (1-10 of 10) with videos related to

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Journal of Visualized Experiments : Jove|May 29, 2023
Nuclei Isolation from Mouse Cardiac Progenitor Cells for Epigenome and Gene Expression Profiling at Single-Cell ResolutionStephanie Ibrahim, Catherine Robert, Camille Humbert, et al.
Ebiomedicine|May 7, 2024
First-in-man use of a cardiovascular cell-derived secretome in heart failure. Case reportPhilippe Menasché, Nisa K Renault, Albert Hagège, et al.
Journal of Extracellular Vesicles|August 20, 2025
GMP-Compliant Process for the Manufacturing of an Extracellular Vesicles-Enriched Secretome Product Derived From Cardiovascular Progenitor Cells Suitable for a Phase I Clinical TrialCamille Humbert, Chloé Cordier, Iouri Drut, et al.
Development (Cambridge, England)|February 10, 2025
Multi-modal refinement of the human heart atlas during the first gestational trimesterChristopher De Bono, Yichi Xu, Samina Kausar, et al.
Frontiers in Cardiovascular Medicine|July 24, 2023
Therapeutic potential of extracellular vesicles derived from cardiac progenitor cells in rodent models of chemotherapy-induced cardiomyopathyManon Desgres, Bruna Lima Correa, Lorena Petrusca, et al.
American Journal of Human Genetics|January 21, 2014
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humansCamille Humbert, Flora Silbermann, Bharti Morar, et al.
Brain : a Journal of Neurology|February 5, 2026
Benchmarking long-read sequencing approaches to resolve facioscapulohumeral dystrophy locus complexityCharlotte Tardy, Jean Philippe Trani, Victor Murcia Pienkowski, et al.
Human Molecular Genetics|May 2, 2019
Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesionMarie Alice Dupont, Camille Humbert, Céline Huber, et al.
Journal of the American Society of Nephrology : JASN|June 2, 2017
Targeted Exome Sequencing Identifies <i>PBX1</i> as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary TractLaurence Heidet, Vincent Morinière, Charline Henry, et al.
American Journal of Human Genetics|November 4, 2017
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and MiceLara De Tomasi, Pierre David, Camille Humbert, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Journal of Visualized Experiments : Jove|May 29, 2023
Nuclei Isolation from Mouse Cardiac Progenitor Cells for Epigenome and Gene Expression Profiling at Single-Cell ResolutionStephanie Ibrahim, Catherine Robert, Camille Humbert, et al.
Ebiomedicine|May 7, 2024
First-in-man use of a cardiovascular cell-derived secretome in heart failure. Case reportPhilippe Menasché, Nisa K Renault, Albert Hagège, et al.
Journal of Extracellular Vesicles|August 20, 2025
GMP-Compliant Process for the Manufacturing of an Extracellular Vesicles-Enriched Secretome Product Derived From Cardiovascular Progenitor Cells Suitable for a Phase I Clinical TrialCamille Humbert, Chloé Cordier, Iouri Drut, et al.
Development (Cambridge, England)|February 10, 2025
Multi-modal refinement of the human heart atlas during the first gestational trimesterChristopher De Bono, Yichi Xu, Samina Kausar, et al.
Frontiers in Cardiovascular Medicine|July 24, 2023
Therapeutic potential of extracellular vesicles derived from cardiac progenitor cells in rodent models of chemotherapy-induced cardiomyopathyManon Desgres, Bruna Lima Correa, Lorena Petrusca, et al.
American Journal of Human Genetics|January 21, 2014
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humansCamille Humbert, Flora Silbermann, Bharti Morar, et al.
Brain : a Journal of Neurology|February 5, 2026
Benchmarking long-read sequencing approaches to resolve facioscapulohumeral dystrophy locus complexityCharlotte Tardy, Jean Philippe Trani, Victor Murcia Pienkowski, et al.
Human Molecular Genetics|May 2, 2019
Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesionMarie Alice Dupont, Camille Humbert, Céline Huber, et al.
Journal of the American Society of Nephrology : JASN|June 2, 2017
Targeted Exome Sequencing Identifies <i>PBX1</i> as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary TractLaurence Heidet, Vincent Morinière, Charline Henry, et al.
American Journal of Human Genetics|November 4, 2017
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and MiceLara De Tomasi, Pierre David, Camille Humbert, et al.
Pageof 1