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Marcel Tawk

Showing results (11-20 of 25) with videos related to

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Plos Genetics|December 1, 2016
Neuronal Ndrg4 Is Essential for Nodes of Ranvier Organization in ZebrafishLaura Fontenas, Flavia De Santis, Vincenzo Di Donato, et al.
Experimental Neurology|October 14, 2003
Synemin expression in developing normal and pathological human retina and lensMarcel Tawk, Matthias Titeux, Catherine Fallet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 11, 2011
Wnt/beta-catenin signaling is an essential and direct driver of myelin gene expression and myelinogenesisMarcel Tawk, Joelle Makoukji, Martin Belle, et al.
Cellular and Molecular Life Sciences : CMLS|June 5, 2019
Elmo1 function, linked to Rac1 activity, regulates peripheral neuronal numbers and myelination in zebrafishAya Mikdache, Laura Fontenas, Shahad Albadri, et al.
Scientific Reports|June 26, 2021
Rgs4 is a regulator of mTOR activity required for motoneuron axon outgrowth and neuronal development in zebrafishAya Mikdache, Marie-José Boueid, Lorijn van der Spek, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 2014
Immunophilin FKBP52 induces Tau-P301L filamentous assembly in vitro and modulates its activity in a model of tauopathyJulien Giustiniani, Béatrice Chambraud, Elodie Sardin, et al.
Nature|March 30, 2007
A mirror-symmetric cell division that orchestrates neuroepithelial morphogenesisMarcel Tawk, Claudio Araya, Dave A Lyons, et al.
Brain : a Journal of Neurology|February 15, 2018
Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformationAlexandre Vivanti, Augustin Ozanne, Cynthia Grondin, et al.
Frontiers in Pediatrics|May 13, 2022
Arteriovenous Cerebral High Flow Shunts in Children: From Genotype to PhenotypeBerivan Tas, Daniele Starnoni, Stanislas Smajda, et al.
American Journal of Human Genetics|June 19, 2012
Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1Jie Zhou, Marcel Tawk, Francesco Danilo Tiziano, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Plos Genetics|December 1, 2016
Neuronal Ndrg4 Is Essential for Nodes of Ranvier Organization in ZebrafishLaura Fontenas, Flavia De Santis, Vincenzo Di Donato, et al.
Experimental Neurology|October 14, 2003
Synemin expression in developing normal and pathological human retina and lensMarcel Tawk, Matthias Titeux, Catherine Fallet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 11, 2011
Wnt/beta-catenin signaling is an essential and direct driver of myelin gene expression and myelinogenesisMarcel Tawk, Joelle Makoukji, Martin Belle, et al.
Cellular and Molecular Life Sciences : CMLS|June 5, 2019
Elmo1 function, linked to Rac1 activity, regulates peripheral neuronal numbers and myelination in zebrafishAya Mikdache, Laura Fontenas, Shahad Albadri, et al.
Scientific Reports|June 26, 2021
Rgs4 is a regulator of mTOR activity required for motoneuron axon outgrowth and neuronal development in zebrafishAya Mikdache, Marie-José Boueid, Lorijn van der Spek, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 2014
Immunophilin FKBP52 induces Tau-P301L filamentous assembly in vitro and modulates its activity in a model of tauopathyJulien Giustiniani, Béatrice Chambraud, Elodie Sardin, et al.
Nature|March 30, 2007
A mirror-symmetric cell division that orchestrates neuroepithelial morphogenesisMarcel Tawk, Claudio Araya, Dave A Lyons, et al.
Brain : a Journal of Neurology|February 15, 2018
Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformationAlexandre Vivanti, Augustin Ozanne, Cynthia Grondin, et al.
Frontiers in Pediatrics|May 13, 2022
Arteriovenous Cerebral High Flow Shunts in Children: From Genotype to PhenotypeBerivan Tas, Daniele Starnoni, Stanislas Smajda, et al.
American Journal of Human Genetics|June 19, 2012
Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1Jie Zhou, Marcel Tawk, Francesco Danilo Tiziano, et al.
Pageof 3