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Christelle M Durand

Showing results (1-10 of 15) with videos related to

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Medecine Sciences : M/S|January 17, 2008
[Alterations in synapsis formation and function in autism disorders]Christelle M Durand, Pauline Chaste, Fabien Fauchereau, et al.
BMC Neurology|February 13, 2022
Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxiaChristelle M Durand, Chloé Angelini, Vincent Michaud, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 28, 2023
Mutation on MT-CO2 gene induces mitochondrial disease associated with neurodegeneration and intracerebral iron accumulation (NBIA)Sarah Courtois, Chloé Angelini, Christelle M Durand, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 28, 2010
The planar polarity protein Scribble1 is essential for neuronal plasticity and brain functionMaïté M Moreau, Nicolas Piguel, Thomas Papouin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 7, 2005
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disordersChristelle M Durand, Caroline Kappeler, Catalina Betancur, et al.
BMC Medical Genetics|January 27, 2009
An investigation of ribosomal protein L10 gene in autism spectrum disordersXiaohong Gong, Richard Delorme, Fabien Fauchereau, et al.
Biological Psychiatry|April 4, 2006
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjectsRichard Delorme, Christelle M Durand, Catalina Betancur, et al.
Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.
Human Mutation|October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Cell Reports|October 15, 2014
Scribble1/AP2 complex coordinates NMDA receptor endocytic recyclingNicolas H Piguel, Sabine Fievre, Jean-Michel Blanc, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Medecine Sciences : M/S|January 17, 2008
[Alterations in synapsis formation and function in autism disorders]Christelle M Durand, Pauline Chaste, Fabien Fauchereau, et al.
BMC Neurology|February 13, 2022
Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxiaChristelle M Durand, Chloé Angelini, Vincent Michaud, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 28, 2023
Mutation on MT-CO2 gene induces mitochondrial disease associated with neurodegeneration and intracerebral iron accumulation (NBIA)Sarah Courtois, Chloé Angelini, Christelle M Durand, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 28, 2010
The planar polarity protein Scribble1 is essential for neuronal plasticity and brain functionMaïté M Moreau, Nicolas Piguel, Thomas Papouin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 7, 2005
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disordersChristelle M Durand, Caroline Kappeler, Catalina Betancur, et al.
BMC Medical Genetics|January 27, 2009
An investigation of ribosomal protein L10 gene in autism spectrum disordersXiaohong Gong, Richard Delorme, Fabien Fauchereau, et al.
Biological Psychiatry|April 4, 2006
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjectsRichard Delorme, Christelle M Durand, Catalina Betancur, et al.
Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.
Human Mutation|October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Cell Reports|October 15, 2014
Scribble1/AP2 complex coordinates NMDA receptor endocytic recyclingNicolas H Piguel, Sabine Fievre, Jean-Michel Blanc, et al.
Pageof 2