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Monnot

Showing results (301-310 of 338) with videos related to

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Science Signaling|July 16, 2015
The interaction of heparan sulfate proteoglycans with endothelial transglutaminase-2 limits VEGF165-induced angiogenesisNathan Beckouche, Marine Bignon, Virginie Lelarge, et al.
The Journal of Biological Chemistry|May 26, 2011
Luminal lipid regulates CD36 levels and downstream signaling to stimulate chylomicron synthesisThi Thu Trang Tran, Hélène Poirier, Lionel Clément, et al.
Human Mutation|December 2, 2010
Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model systemSophie Monnot, Nadine Gigarel, David C Samuels, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosisF Habarou, A Brassier, M Rio, et al.
British Journal of Clinical Pharmacology|March 24, 2021
Safety, tolerability and pharmacokinetics of emodepside, a potential novel treatment for onchocerciasis (river blindness), in healthy male subjectsJean-Yves Gillon, Jeremy Dennison, Frans van den Berg, et al.
Blood|August 13, 2011
Lysyl oxidase-like protein-2 regulates sprouting angiogenesis and type IV collagen assembly in the endothelial basement membraneMarine Bignon, Cathy Pichol-Thievend, Julie Hardouin, et al.
Science Immunology|January 5, 2020
Human T cell response to CD1a and contact dermatitis allergens in botanical extracts and commercial skin care productsSarah Nicolai, Marcin Wegrecki, Tan-Yun Cheng, et al.
Clinical Genetics|June 26, 2019
Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature reviewVaroona Bizaoui, Caroline Michot, Geneviève Baujat, et al.
Acta Biomaterialia|July 5, 2023
Papillary and reticular fibroblasts generate distinct microenvironments that differentially impact angiogenesisAdèle Mauroux, Pauline Joncour, Noémie Brassard-Jollive, et al.
Journal of Medical Genetics|July 30, 2017
Segregation of mitochondrial DNA mutations in the human placenta: implication for prenatal diagnosis of mtDNA disordersPauline Vachin, Elodie Adda-Herzog, Gihad Chalouhi, et al.
Pageof 34

Showing results (301-310 of 338) with videos related to

Sort By:
Pageof 34
Science Signaling|July 16, 2015
The interaction of heparan sulfate proteoglycans with endothelial transglutaminase-2 limits VEGF165-induced angiogenesisNathan Beckouche, Marine Bignon, Virginie Lelarge, et al.
The Journal of Biological Chemistry|May 26, 2011
Luminal lipid regulates CD36 levels and downstream signaling to stimulate chylomicron synthesisThi Thu Trang Tran, Hélène Poirier, Lionel Clément, et al.
Human Mutation|December 2, 2010
Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model systemSophie Monnot, Nadine Gigarel, David C Samuels, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosisF Habarou, A Brassier, M Rio, et al.
British Journal of Clinical Pharmacology|March 24, 2021
Safety, tolerability and pharmacokinetics of emodepside, a potential novel treatment for onchocerciasis (river blindness), in healthy male subjectsJean-Yves Gillon, Jeremy Dennison, Frans van den Berg, et al.
Blood|August 13, 2011
Lysyl oxidase-like protein-2 regulates sprouting angiogenesis and type IV collagen assembly in the endothelial basement membraneMarine Bignon, Cathy Pichol-Thievend, Julie Hardouin, et al.
Science Immunology|January 5, 2020
Human T cell response to CD1a and contact dermatitis allergens in botanical extracts and commercial skin care productsSarah Nicolai, Marcin Wegrecki, Tan-Yun Cheng, et al.
Clinical Genetics|June 26, 2019
Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature reviewVaroona Bizaoui, Caroline Michot, Geneviève Baujat, et al.
Acta Biomaterialia|July 5, 2023
Papillary and reticular fibroblasts generate distinct microenvironments that differentially impact angiogenesisAdèle Mauroux, Pauline Joncour, Noémie Brassard-Jollive, et al.
Journal of Medical Genetics|July 30, 2017
Segregation of mitochondrial DNA mutations in the human placenta: implication for prenatal diagnosis of mtDNA disordersPauline Vachin, Elodie Adda-Herzog, Gihad Chalouhi, et al.
Pageof 34