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Pierre Billuart

Showing results (41-50 of 45) with videos related to

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Science (New York, N.Y.)|July 2, 2021
Astrocytes close the mouse critical period for visual plasticityJérôme Ribot, Rachel Breton, Charles-Félix Calvo, et al.
Current Biology : CB|January 26, 2010
A postsynaptic signaling pathway that may account for the cognitive defect due to IL1RAPL1 mutationAlice Pavlowsky, Antonella Gianfelice, Marta Pallotto, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|December 4, 2013
Lack of the presynaptic RhoGAP protein oligophrenin1 leads to cognitive disabilities through dysregulation of the cAMP/PKA signalling pathwayMalik Khelfaoui, Frédéric Gambino, Xander Houbaert, et al.
Cell Reports|April 18, 2019
IL-38 Ameliorates Skin Inflammation and Limits IL-17 Production from γδ T CellsYingying Han, Javier Mora, Arnaud Huard, et al.
Human Molecular Genetics|October 12, 2014
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisMariana Ramos-Brossier, Caterina Montani, Nicolas Lebrun, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Science (New York, N.Y.)|July 2, 2021
Astrocytes close the mouse critical period for visual plasticityJérôme Ribot, Rachel Breton, Charles-Félix Calvo, et al.
Current Biology : CB|January 26, 2010
A postsynaptic signaling pathway that may account for the cognitive defect due to IL1RAPL1 mutationAlice Pavlowsky, Antonella Gianfelice, Marta Pallotto, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|December 4, 2013
Lack of the presynaptic RhoGAP protein oligophrenin1 leads to cognitive disabilities through dysregulation of the cAMP/PKA signalling pathwayMalik Khelfaoui, Frédéric Gambino, Xander Houbaert, et al.
Cell Reports|April 18, 2019
IL-38 Ameliorates Skin Inflammation and Limits IL-17 Production from γδ T CellsYingying Han, Javier Mora, Arnaud Huard, et al.
Human Molecular Genetics|October 12, 2014
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisMariana Ramos-Brossier, Caterina Montani, Nicolas Lebrun, et al.
Pageof 5