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Pierre Drapeau

Showing results (71-80 of 97) with videos related to

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Plos Genetics|December 6, 2008
Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cordAlexandre Montpetit, Stéphanie Côté, Edna Brustein, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|July 26, 2019
The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral SclerosisPoulomee Bose, Elsa Tremblay, Claudia Maios, et al.
Proceedings. Biological Sciences|July 31, 2015
A spatial theory for characterizing predator-multiprey interactions in heterogeneous landscapesDaniel Fortin, Pietro-Luciano Buono, Oswald J Schmitz, et al.
American Journal of Human Genetics|December 13, 2006
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegiaPaul N Valdmanis, Inge A Meijer, Annie Reynolds, et al.
Current Biology : CB|June 5, 2018
Non-canonical mTOR-Independent Role of DEPDC5 in Regulating GABAergic Network DevelopmentAmrutha Swaminathan, Rahma Hassan-Abdi, Solène Renault, et al.
Human Molecular Genetics|June 19, 2008
Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafishFrancois Gros-Louis, Jasna Kriz, Edor Kabashi, et al.
Human Molecular Genetics|December 5, 2009
Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivoEdor Kabashi, Li Lin, Miranda L Tradewell, et al.
Human Molecular Genetics|January 9, 2016
Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organismsCarl Julien, Alexandra Lissouba, Surya Madabattula, et al.
The New England Journal of Medicine|April 6, 2007
Mutations in VANGL1 associated with neural-tube defectsZoha Kibar, Elena Torban, Jonathan R McDearmid, et al.
Development (Cambridge, England)|October 17, 2024
Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesisMingqin Wang, Sen Zhao, Chenjun Shi, et al.
Pageof 10

Showing results (71-80 of 97) with videos related to

Sort By:
Pageof 10
Plos Genetics|December 6, 2008
Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cordAlexandre Montpetit, Stéphanie Côté, Edna Brustein, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|July 26, 2019
The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral SclerosisPoulomee Bose, Elsa Tremblay, Claudia Maios, et al.
Proceedings. Biological Sciences|July 31, 2015
A spatial theory for characterizing predator-multiprey interactions in heterogeneous landscapesDaniel Fortin, Pietro-Luciano Buono, Oswald J Schmitz, et al.
American Journal of Human Genetics|December 13, 2006
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegiaPaul N Valdmanis, Inge A Meijer, Annie Reynolds, et al.
Current Biology : CB|June 5, 2018
Non-canonical mTOR-Independent Role of DEPDC5 in Regulating GABAergic Network DevelopmentAmrutha Swaminathan, Rahma Hassan-Abdi, Solène Renault, et al.
Human Molecular Genetics|June 19, 2008
Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafishFrancois Gros-Louis, Jasna Kriz, Edor Kabashi, et al.
Human Molecular Genetics|December 5, 2009
Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivoEdor Kabashi, Li Lin, Miranda L Tradewell, et al.
Human Molecular Genetics|January 9, 2016
Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organismsCarl Julien, Alexandra Lissouba, Surya Madabattula, et al.
The New England Journal of Medicine|April 6, 2007
Mutations in VANGL1 associated with neural-tube defectsZoha Kibar, Elena Torban, Jonathan R McDearmid, et al.
Development (Cambridge, England)|October 17, 2024
Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesisMingqin Wang, Sen Zhao, Chenjun Shi, et al.
Pageof 10