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Plos Genetics
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December 1, 2016
Neuronal Ndrg4 Is Essential for Nodes of Ranvier Organization in Zebrafish
Laura Fontenas, Flavia De Santis, Vincenzo Di Donato, et al.
Experimental Neurology
|
October 14, 2003
Synemin expression in developing normal and pathological human retina and lens
Marcel 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 myelinogenesis
Marcel 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 zebrafish
Aya 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 zebrafish
Aya 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 tauopathy
Julien Giustiniani, Béatrice Chambraud, Elodie Sardin, et al.
Nature
|
March 30, 2007
A mirror-symmetric cell division that orchestrates neuroepithelial morphogenesis
Marcel 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 malformation
Alexandre Vivanti, Augustin Ozanne, Cynthia Grondin, et al.
Frontiers in Pediatrics
|
May 13, 2022
Arteriovenous Cerebral High Flow Shunts in Children: From Genotype to Phenotype
Berivan 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 ASAH1
Jie Zhou, Marcel Tawk, Francesco Danilo Tiziano, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Plos Genetics
|
December 1, 2016
Neuronal Ndrg4 Is Essential for Nodes of Ranvier Organization in Zebrafish
Laura Fontenas, Flavia De Santis, Vincenzo Di Donato, et al.
Experimental Neurology
|
October 14, 2003
Synemin expression in developing normal and pathological human retina and lens
Marcel 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 myelinogenesis
Marcel 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 zebrafish
Aya 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 zebrafish
Aya 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 tauopathy
Julien Giustiniani, Béatrice Chambraud, Elodie Sardin, et al.
Nature
|
March 30, 2007
A mirror-symmetric cell division that orchestrates neuroepithelial morphogenesis
Marcel 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 malformation
Alexandre Vivanti, Augustin Ozanne, Cynthia Grondin, et al.
Frontiers in Pediatrics
|
May 13, 2022
Arteriovenous Cerebral High Flow Shunts in Children: From Genotype to Phenotype
Berivan 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 ASAH1
Jie Zhou, Marcel Tawk, Francesco Danilo Tiziano, et al.
Page
of 3