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Elisabeth Bouché

Showing results (1-10 of 10) with videos related to

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The European Journal of Neuroscience|April 21, 2007
Candidate pheromone receptors provide the basis for the response of distinct antennal neurons to pheromonal compoundsEwald Grosse-Wilde, Thomas Gohl, Elisabeth Bouché, et al.
Plos One|August 27, 2013
ApoER2 and VLDLr are required for mediating reelin signalling pathway for normal migration and positioning of mesencephalic dopaminergic neuronsAhmed Sharaf, Hans H Bock, Björn Spittau, et al.
Plos One|October 20, 2017
Mathematical model of early Reelin-induced Src family kinase-mediated signalingHelge Hass, Friederike Kipkeew, Aziz Gauhar, et al.
The European Journal of Neuroscience|November 3, 2010
Role for Reelin-induced cofilin phosphorylation in the assembly of sympathetic preganglionic neurons in the murine intermediolateral columnMarie T Krüger, Shanting Zhao, Xuejun Chai, et al.
Cell Research|January 16, 2013
Reelin induces EphB activationElisabeth Bouché, Mario I Romero-Ortega, Mark Henkemeyer, et al.
Glia|July 6, 2013
Role of the postnatal radial glial scaffold for the development of the dentate gyrus as revealed by Reelin signaling mutant miceBianka Brunne, Santos Franco, Elisabeth Bouché, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 28, 2013
Characterization and distribution of Reelin-positive interneuron subtypes in the rat barrel cortexTheresa Pohlkamp, Csaba Dávid, Bruno Cauli, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 2010
Reelin signals through apolipoprotein E receptor 2 and Cdc42 to increase growth cone motility and filopodia formationJost Leemhuis, Elisabeth Bouché, Michael Frotscher, et al.
Neurogenetics|January 7, 2012
Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalusMariola Marx, Simone Diestel, Muriel Bozon, et al.
Neurobiology of Disease|July 13, 2010
L1 syndrome mutations impair neuronal L1 function at different levels by divergent mechanismsMichael K E Schäfer, Yun-Chung Nam, Anice Moumen, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
The European Journal of Neuroscience|April 21, 2007
Candidate pheromone receptors provide the basis for the response of distinct antennal neurons to pheromonal compoundsEwald Grosse-Wilde, Thomas Gohl, Elisabeth Bouché, et al.
Plos One|August 27, 2013
ApoER2 and VLDLr are required for mediating reelin signalling pathway for normal migration and positioning of mesencephalic dopaminergic neuronsAhmed Sharaf, Hans H Bock, Björn Spittau, et al.
Plos One|October 20, 2017
Mathematical model of early Reelin-induced Src family kinase-mediated signalingHelge Hass, Friederike Kipkeew, Aziz Gauhar, et al.
The European Journal of Neuroscience|November 3, 2010
Role for Reelin-induced cofilin phosphorylation in the assembly of sympathetic preganglionic neurons in the murine intermediolateral columnMarie T Krüger, Shanting Zhao, Xuejun Chai, et al.
Cell Research|January 16, 2013
Reelin induces EphB activationElisabeth Bouché, Mario I Romero-Ortega, Mark Henkemeyer, et al.
Glia|July 6, 2013
Role of the postnatal radial glial scaffold for the development of the dentate gyrus as revealed by Reelin signaling mutant miceBianka Brunne, Santos Franco, Elisabeth Bouché, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 28, 2013
Characterization and distribution of Reelin-positive interneuron subtypes in the rat barrel cortexTheresa Pohlkamp, Csaba Dávid, Bruno Cauli, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 2010
Reelin signals through apolipoprotein E receptor 2 and Cdc42 to increase growth cone motility and filopodia formationJost Leemhuis, Elisabeth Bouché, Michael Frotscher, et al.
Neurogenetics|January 7, 2012
Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalusMariola Marx, Simone Diestel, Muriel Bozon, et al.
Neurobiology of Disease|July 13, 2010
L1 syndrome mutations impair neuronal L1 function at different levels by divergent mechanismsMichael K E Schäfer, Yun-Chung Nam, Anice Moumen, et al.
Pageof 1