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Nadia Messaddeq

Showing results (11-20 of 108) with videos related to

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Human Molecular Genetics|December 22, 2018
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in miceRoberto Silva-Rojas, Susan Treves, Hugues Jacobs, et al.
In Vivo (Athens, Greece)|February 2, 2011
Cell death after high-LET irradiation in orthotopic human hepatocellular carcinoma in vivoAnaïs Altmeyer, Mihaela Ignat, Jean-Marc Denis, et al.
International Journal of Nanomedicine|July 16, 2011
Microencapsulation of nanoemulsions: novel Trojan particles for bioactive lipid molecule deliveryXiang Li, Nicolas Anton, Thi Minh Chau Ta, et al.
Diabetes|July 13, 2022
PATAS, a First-in-Class Therapeutic Peptide Biologic, Improves Whole-Body Insulin Resistance and Associated Comorbidities In VivoEdwige Schreyer, Cathy Obringer, Nadia Messaddeq, et al.
Circulation|June 18, 2003
Overexpression of the serotonin 5-HT2B receptor in heart leads to abnormal mitochondrial function and cardiac hypertrophyCanan G Nebigil, Fabrice Jaffré, Nadia Messaddeq, et al.
American Journal of Physiology. Heart and Circulatory Physiology|December 22, 2009
Divergent roles of prokineticin receptors in the endothelial cells: angiogenesis and fenestrationCélia Guilini, Kyoji Urayama, Gulen Turkeri, et al.
Developmental Biology|July 26, 2005
TAF10 is required for the establishment of skin barrier function in foetal, but not in adult mouse epidermisArup Kumar Indra, William S Mohan, Mattia Frontini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 23, 2013
Lack of myotubularin (MTM1) leads to muscle hypotrophy through unbalanced regulation of the autophagy and ubiquitin-proteasome pathwaysLama Al-Qusairi, Ivana Prokic, Leonela Amoasii, et al.
Biochimica Et Biophysica Acta|December 17, 2008
Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasiaStéphanie Pannier, Vincent Couloigner, Nadia Messaddeq, et al.
Cardiovascular Research|September 23, 2008
Transgenic myocardial overexpression of prokineticin receptor-2 (GPR73b) induces hypertrophy and capillary vessel leakageKyoji Urayama, Deniz B Dedeoglu, Célia Guilini, et al.
Pageof 11

Showing results (11-20 of 108) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|December 22, 2018
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in miceRoberto Silva-Rojas, Susan Treves, Hugues Jacobs, et al.
In Vivo (Athens, Greece)|February 2, 2011
Cell death after high-LET irradiation in orthotopic human hepatocellular carcinoma in vivoAnaïs Altmeyer, Mihaela Ignat, Jean-Marc Denis, et al.
International Journal of Nanomedicine|July 16, 2011
Microencapsulation of nanoemulsions: novel Trojan particles for bioactive lipid molecule deliveryXiang Li, Nicolas Anton, Thi Minh Chau Ta, et al.
Diabetes|July 13, 2022
PATAS, a First-in-Class Therapeutic Peptide Biologic, Improves Whole-Body Insulin Resistance and Associated Comorbidities In VivoEdwige Schreyer, Cathy Obringer, Nadia Messaddeq, et al.
Circulation|June 18, 2003
Overexpression of the serotonin 5-HT2B receptor in heart leads to abnormal mitochondrial function and cardiac hypertrophyCanan G Nebigil, Fabrice Jaffré, Nadia Messaddeq, et al.
American Journal of Physiology. Heart and Circulatory Physiology|December 22, 2009
Divergent roles of prokineticin receptors in the endothelial cells: angiogenesis and fenestrationCélia Guilini, Kyoji Urayama, Gulen Turkeri, et al.
Developmental Biology|July 26, 2005
TAF10 is required for the establishment of skin barrier function in foetal, but not in adult mouse epidermisArup Kumar Indra, William S Mohan, Mattia Frontini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 23, 2013
Lack of myotubularin (MTM1) leads to muscle hypotrophy through unbalanced regulation of the autophagy and ubiquitin-proteasome pathwaysLama Al-Qusairi, Ivana Prokic, Leonela Amoasii, et al.
Biochimica Et Biophysica Acta|December 17, 2008
Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasiaStéphanie Pannier, Vincent Couloigner, Nadia Messaddeq, et al.
Cardiovascular Research|September 23, 2008
Transgenic myocardial overexpression of prokineticin receptor-2 (GPR73b) induces hypertrophy and capillary vessel leakageKyoji Urayama, Deniz B Dedeoglu, Célia Guilini, et al.
Pageof 11