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Charles Fouillade

Showing results (1-10 of 31) with videos related to

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The European Respiratory Journal|November 5, 2021
PD-L1<sup>high</sup> AT2 cells: a new player for alveoli regenerationCharles Fouillade, Arturo Londoño-Vallejo
Medecine Sciences : M/S|March 7, 2015
[The radiotherapy FLASH to save healthy tissues]Vincent Favaudon, Charles Fouillade, Marie-Catherine Vozenin
Methods in Molecular Biology (Clifton, N.J.)|November 11, 2024
Homebuilt Imaging-Based Spatial Transcriptomics: Tertiary Lymphoid Structures as a Case ExampleThomas Defard, Auxence Desrentes, Charles Fouillade, et al.
Cardiovascular Research|January 24, 2012
Notch signalling in smooth muscle cells during development and diseaseCharles Fouillade, Marie Monet-Leprêtre, Céline Baron-Menguy, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|April 20, 2019
Simulation and experimental validation of a prototype electron beam linear accelerator for preclinical studiesPierre Lansonneur, Vincent Favaudon, Sophie Heinrich, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|September 29, 2024
A multidisciplinary view of flash irradiationFlavia Gesualdi, Ludovic de Marzi, Marie Dutreix, et al.
The European Respiratory Journal|April 9, 2021
Spatial transcriptomics for respiratory research and medicineSandra Curras-Alonso, Juliette Soulier, Thomas Walter, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 3, 2012
Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculatureCharles Fouillade, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Human Mutation|February 15, 2008
Activating NOTCH3 mutation in a patient with small-vessel-disease of the brainCharles Fouillade, Hugues Chabriat, Florence Riant, et al.
Stroke|January 16, 2014
Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanismEmmanuel Cognat, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
The European Respiratory Journal|November 5, 2021
PD-L1<sup>high</sup> AT2 cells: a new player for alveoli regenerationCharles Fouillade, Arturo Londoño-Vallejo
Medecine Sciences : M/S|March 7, 2015
[The radiotherapy FLASH to save healthy tissues]Vincent Favaudon, Charles Fouillade, Marie-Catherine Vozenin
Methods in Molecular Biology (Clifton, N.J.)|November 11, 2024
Homebuilt Imaging-Based Spatial Transcriptomics: Tertiary Lymphoid Structures as a Case ExampleThomas Defard, Auxence Desrentes, Charles Fouillade, et al.
Cardiovascular Research|January 24, 2012
Notch signalling in smooth muscle cells during development and diseaseCharles Fouillade, Marie Monet-Leprêtre, Céline Baron-Menguy, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|April 20, 2019
Simulation and experimental validation of a prototype electron beam linear accelerator for preclinical studiesPierre Lansonneur, Vincent Favaudon, Sophie Heinrich, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|September 29, 2024
A multidisciplinary view of flash irradiationFlavia Gesualdi, Ludovic de Marzi, Marie Dutreix, et al.
The European Respiratory Journal|April 9, 2021
Spatial transcriptomics for respiratory research and medicineSandra Curras-Alonso, Juliette Soulier, Thomas Walter, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 3, 2012
Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculatureCharles Fouillade, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Human Mutation|February 15, 2008
Activating NOTCH3 mutation in a patient with small-vessel-disease of the brainCharles Fouillade, Hugues Chabriat, Florence Riant, et al.
Stroke|January 16, 2014
Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanismEmmanuel Cognat, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Pageof 4