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Nadia Messaddeq

Showing results (51-60 of 108) with videos related to

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Soft Matter|October 22, 2019
Correction: Pickering nano-emulsions stabilized by solid lipid nanoparticles as a temperature sensitive drug delivery systemSidy Mouhamed Dieng, Nicolas Anton, Patrick Bouriat, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 5, 2009
Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiationVincent Marion, Corinne Stoetzel, Dominique Schlicht, et al.
Journal of the American Heart Association|October 25, 2013
Prokineticin receptor-1 is a new regulator of endothelial insulin uptake and capillary formation to control insulin sensitivity and cardiovascular and kidney functionsMojdeh Dormishian, Gulen Turkeri, Kyoji Urayama, et al.
Cell and Tissue Research|September 8, 2016
Well-organized spheroids as a new platform to examine cell interaction and behaviour during organ developmentThibault Bécavin, Sabine Kuchler-Bopp, Tunay Kökten, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 29, 2011
Genetic inactivation of prokineticin receptor-1 leads to heart and kidney disordersMounia Boulberdaa, Gulen Turkeri, Kyoji Urayama, et al.
Acta Biomaterialia|November 14, 2017
A new formulation of poly(MAOTIB) nanoparticles as an efficient contrast agent for in vivo X-ray imagingJustine Wallyn, Nicolas Anton, Christophe A Serra, et al.
Human Molecular Genetics|August 6, 2016
Myelinosomes act as natural secretory organelles in Sertoli cells to prevent accumulation of aggregate-prone mutant Huntingtin and CFTRMarina G Yefimova, Emile Béré, Anne Cantereau-Becq, et al.
Plos One|July 25, 2009
The first cellular models based on frataxin missense mutations that reproduce spontaneously the defects associated with Friedreich ataxiaNadège Calmels, Stéphane Schmucker, Marie Wattenhofer-Donzé, et al.
Experimental Eye Research|July 15, 2019
In vivo phenotypic and molecular characterization of retinal degeneration in mouse models of three ciliopathiesAgnès Brun, Xiangxiang Yu, Cathy Obringer, et al.
The Journal of Clinical Endocrinology and Metabolism|August 25, 2020
Reproduction Function in Male Patients With Bardet Biedl SyndromeIsabelle Koscinski, Manuel Mark, Nadia Messaddeq, et al.
Pageof 11

Showing results (51-60 of 108) with videos related to

Sort By:
Pageof 11
Soft Matter|October 22, 2019
Correction: Pickering nano-emulsions stabilized by solid lipid nanoparticles as a temperature sensitive drug delivery systemSidy Mouhamed Dieng, Nicolas Anton, Patrick Bouriat, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 5, 2009
Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiationVincent Marion, Corinne Stoetzel, Dominique Schlicht, et al.
Journal of the American Heart Association|October 25, 2013
Prokineticin receptor-1 is a new regulator of endothelial insulin uptake and capillary formation to control insulin sensitivity and cardiovascular and kidney functionsMojdeh Dormishian, Gulen Turkeri, Kyoji Urayama, et al.
Cell and Tissue Research|September 8, 2016
Well-organized spheroids as a new platform to examine cell interaction and behaviour during organ developmentThibault Bécavin, Sabine Kuchler-Bopp, Tunay Kökten, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 29, 2011
Genetic inactivation of prokineticin receptor-1 leads to heart and kidney disordersMounia Boulberdaa, Gulen Turkeri, Kyoji Urayama, et al.
Acta Biomaterialia|November 14, 2017
A new formulation of poly(MAOTIB) nanoparticles as an efficient contrast agent for in vivo X-ray imagingJustine Wallyn, Nicolas Anton, Christophe A Serra, et al.
Human Molecular Genetics|August 6, 2016
Myelinosomes act as natural secretory organelles in Sertoli cells to prevent accumulation of aggregate-prone mutant Huntingtin and CFTRMarina G Yefimova, Emile Béré, Anne Cantereau-Becq, et al.
Plos One|July 25, 2009
The first cellular models based on frataxin missense mutations that reproduce spontaneously the defects associated with Friedreich ataxiaNadège Calmels, Stéphane Schmucker, Marie Wattenhofer-Donzé, et al.
Experimental Eye Research|July 15, 2019
In vivo phenotypic and molecular characterization of retinal degeneration in mouse models of three ciliopathiesAgnès Brun, Xiangxiang Yu, Cathy Obringer, et al.
The Journal of Clinical Endocrinology and Metabolism|August 25, 2020
Reproduction Function in Male Patients With Bardet Biedl SyndromeIsabelle Koscinski, Manuel Mark, Nadia Messaddeq, et al.
Pageof 11