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Showing results (671-680 of 685) with videos related to

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Science Immunology|November 15, 2024
A tetraspecific engager armed with a non-alpha IL-2 variant harnesses natural killer cells against B cell non-Hodgkin lymphomaOlivier Demaria, Guillaume Habif, Marie Vetizou, et al.
Nature Communications|September 3, 2022
Identification of risk loci for primary aldosteronism in genome-wide association studiesEdith Le Floch, Teresa Cosentino, Casper K Larsen, et al.
European Journal of Heart Failure|April 14, 2016
Traditional and new composite endpoints in heart failure clinical trials: facilitating comprehensive efficacy assessments and improving trial efficiencyStefan D Anker, Stefan Schroeder, Dan Atar, et al.
Medrxiv : the Preprint Server for Health Sciences|May 2, 2025
Clinical translation of ultrasoft Fleuron probes for stable, high-density, and bidirectional brain interfacesJongha Lee, Hyunsu Park, Andrew Spencer, et al.
Journal of Neurointerventional Surgery|December 2, 2022
Influence of prior intravenous thrombolysis in patients treated with mechanical thrombectomy for M2 occlusions: insight from the Endovascular Treatment in Ischemic Stroke (ETIS) registryAgathe Le Floch, Frédéric Clarençon, Aymeric Rouchaud, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2026
Disparate social structures are underpinned by distinct social rules across a primate radiationJacob A Feder, Susan C Alberts, Elizabeth A Archie, et al.
Nature Communications|August 7, 2024
Human genetic structure in Northwest France provides new insights into West European historical demographyIsabel Alves, Joanna Giemza, Michael G B Blum, et al.
Scientific Data|March 2, 2026
Wheat historical phenotypic data from European genebanks as an important resource for research and breedingErwan Le Floch, Anne-Françoise Adam-Blondon, Michael Alaux, et al.
Human Mutation|March 3, 2019
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disordersChristina Zeitz, Christelle Michiels, Marion Neuillé, et al.
European Journal of Cancer (Oxford, England : 1990)|December 12, 2022
Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the diseaseYue Jiao, Thérèse Truong, Séverine Eon-Marchais, et al.
Pageof 69

Showing results (671-680 of 685) with videos related to

Sort By:
Pageof 69
Science Immunology|November 15, 2024
A tetraspecific engager armed with a non-alpha IL-2 variant harnesses natural killer cells against B cell non-Hodgkin lymphomaOlivier Demaria, Guillaume Habif, Marie Vetizou, et al.
Nature Communications|September 3, 2022
Identification of risk loci for primary aldosteronism in genome-wide association studiesEdith Le Floch, Teresa Cosentino, Casper K Larsen, et al.
European Journal of Heart Failure|April 14, 2016
Traditional and new composite endpoints in heart failure clinical trials: facilitating comprehensive efficacy assessments and improving trial efficiencyStefan D Anker, Stefan Schroeder, Dan Atar, et al.
Medrxiv : the Preprint Server for Health Sciences|May 2, 2025
Clinical translation of ultrasoft Fleuron probes for stable, high-density, and bidirectional brain interfacesJongha Lee, Hyunsu Park, Andrew Spencer, et al.
Journal of Neurointerventional Surgery|December 2, 2022
Influence of prior intravenous thrombolysis in patients treated with mechanical thrombectomy for M2 occlusions: insight from the Endovascular Treatment in Ischemic Stroke (ETIS) registryAgathe Le Floch, Frédéric Clarençon, Aymeric Rouchaud, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2026
Disparate social structures are underpinned by distinct social rules across a primate radiationJacob A Feder, Susan C Alberts, Elizabeth A Archie, et al.
Nature Communications|August 7, 2024
Human genetic structure in Northwest France provides new insights into West European historical demographyIsabel Alves, Joanna Giemza, Michael G B Blum, et al.
Scientific Data|March 2, 2026
Wheat historical phenotypic data from European genebanks as an important resource for research and breedingErwan Le Floch, Anne-Françoise Adam-Blondon, Michael Alaux, et al.
Human Mutation|March 3, 2019
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disordersChristina Zeitz, Christelle Michiels, Marion Neuillé, et al.
European Journal of Cancer (Oxford, England : 1990)|December 12, 2022
Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the diseaseYue Jiao, Thérèse Truong, Séverine Eon-Marchais, et al.
Pageof 69