Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Pierre Billuart

Showing results (1-10 of 45) with videos related to

Pageof 5
Sort By:
Neuron|June 24, 2003
From fragile X mental retardation protein to Rac1 GTPase: new insights from Fly CYFIPPierre Billuart, Jamel Chelly
Medecine Sciences : M/S|October 7, 2020
[A role for astrocytes in intellectual disabilities?]Noémie Cresto, Pierre Billuart, Nathalie Rouach
Medecine Sciences : M/S|November 9, 2005
[X-linked mental retardation]Pierre Billuart, Jamel Chelly, Simone Gilgenkrantz
Trends in Neurosciences|July 14, 2019
Do Astrocytes Play a Role in Intellectual Disabilities?Noémie Cresto, Laure-Elise Pillet, Pierre Billuart, et al.
Journal of Molecular Neuroscience : MN|January 31, 2015
Differential Expression and Regulation of Brain-Derived Neurotrophic Factor (BDNF) mRNA Isoforms in Brain Cells from Mecp2(308/y) Mouse ModelAudrey Rousseaud, Chloé Delépine, Juliette Nectoux, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Loss of Function of KCNC1 is associated with intellectual disability without seizuresKarine Poirier, Géraldine Viot, Laura Lombardi, et al.
Cells|May 14, 2022
Hippocampal Excitatory Synaptic Transmission and Plasticity Are Differentially Altered during Postnatal Development by Loss of the X-Linked Intellectual Disability Protein Oligophrenin-1Noemie Cresto, Nicolas Lebrun, Florent Dumont, et al.
American Journal of Medical Genetics. Part A|September 12, 2015
Early-onset encephalopathy with epilepsy associated with a novel splice site mutation in SMC1ANicolas Lebrun, Sébastien Lebon, Pierre-Yves Jeannet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 27, 2020
ROCK/PKA Inhibition Rescues Hippocampal Hyperexcitability and GABAergic Neuron Alterations in a Oligophrenin-1 Knock-Out Mouse Model of X-Linked Intellectual DisabilityIrene Busti, Manuela Allegra, Cristina Spalletti, et al.
Human Mutation|June 7, 2017
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsyKarine Poirier, Laurence Hubert, Géraldine Viot, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Neuron|June 24, 2003
From fragile X mental retardation protein to Rac1 GTPase: new insights from Fly CYFIPPierre Billuart, Jamel Chelly
Medecine Sciences : M/S|October 7, 2020
[A role for astrocytes in intellectual disabilities?]Noémie Cresto, Pierre Billuart, Nathalie Rouach
Medecine Sciences : M/S|November 9, 2005
[X-linked mental retardation]Pierre Billuart, Jamel Chelly, Simone Gilgenkrantz
Trends in Neurosciences|July 14, 2019
Do Astrocytes Play a Role in Intellectual Disabilities?Noémie Cresto, Laure-Elise Pillet, Pierre Billuart, et al.
Journal of Molecular Neuroscience : MN|January 31, 2015
Differential Expression and Regulation of Brain-Derived Neurotrophic Factor (BDNF) mRNA Isoforms in Brain Cells from Mecp2(308/y) Mouse ModelAudrey Rousseaud, Chloé Delépine, Juliette Nectoux, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Loss of Function of KCNC1 is associated with intellectual disability without seizuresKarine Poirier, Géraldine Viot, Laura Lombardi, et al.
Cells|May 14, 2022
Hippocampal Excitatory Synaptic Transmission and Plasticity Are Differentially Altered during Postnatal Development by Loss of the X-Linked Intellectual Disability Protein Oligophrenin-1Noemie Cresto, Nicolas Lebrun, Florent Dumont, et al.
American Journal of Medical Genetics. Part A|September 12, 2015
Early-onset encephalopathy with epilepsy associated with a novel splice site mutation in SMC1ANicolas Lebrun, Sébastien Lebon, Pierre-Yves Jeannet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 27, 2020
ROCK/PKA Inhibition Rescues Hippocampal Hyperexcitability and GABAergic Neuron Alterations in a Oligophrenin-1 Knock-Out Mouse Model of X-Linked Intellectual DisabilityIrene Busti, Manuela Allegra, Cristina Spalletti, et al.
Human Mutation|June 7, 2017
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsyKarine Poirier, Laurence Hubert, Géraldine Viot, et al.
Pageof 5