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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 7, 2015
Oligophrenin-1 Connects Exocytotic Fusion to Compensatory Endocytosis in Neuroendocrine Cells
Sébastien Houy, Catherine Estay-Ahumada, Pauline Croisé, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 23, 2013
Target-specific vulnerability of excitatory synapses leads to deficits in associative memory in a model of intellectual disorder
Xander Houbaert, Chun-Lei Zhang, Frédéric Gambino, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 15, 2017
Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 Deficiency
Chun-Lei Zhang, Mattia Aime, Emilie Laheranne, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
June 4, 2017
The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity
Caterina Montani, Mariana Ramos-Brossier, Luisa Ponzoni, et al.
Biological Psychiatry
|
September 13, 2023
Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization
Vittoria Mariano, Alexandros K Kanellopoulos, Carlotta Ricci, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 31, 2007
Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity
Malik Khelfaoui, Cécile Denis, Elly van Galen, et al.
Human Molecular Genetics
|
May 6, 2016
Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability
Hamid Meziane, Malik Khelfaoui, Noemi Morello, et al.
Biomedicines
|
December 23, 2022
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models
Hamid Meziane, Marie-Christine Birling, Olivia Wendling, et al.
International Journal of Molecular Sciences
|
March 29, 2023
Activation of the PI3K/AKT/mTOR Pathway in Cajal-Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures
Nasim Ramezanidoraki, Driss El Ouardi, Margaux Le, et al.
Human Molecular Genetics
|
November 26, 2015
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
Chloé Delépine, Hamid Meziane, Juliette Nectoux, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 7, 2015
Oligophrenin-1 Connects Exocytotic Fusion to Compensatory Endocytosis in Neuroendocrine Cells
Sébastien Houy, Catherine Estay-Ahumada, Pauline Croisé, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 23, 2013
Target-specific vulnerability of excitatory synapses leads to deficits in associative memory in a model of intellectual disorder
Xander Houbaert, Chun-Lei Zhang, Frédéric Gambino, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 15, 2017
Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 Deficiency
Chun-Lei Zhang, Mattia Aime, Emilie Laheranne, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
June 4, 2017
The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity
Caterina Montani, Mariana Ramos-Brossier, Luisa Ponzoni, et al.
Biological Psychiatry
|
September 13, 2023
Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization
Vittoria Mariano, Alexandros K Kanellopoulos, Carlotta Ricci, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 31, 2007
Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity
Malik Khelfaoui, Cécile Denis, Elly van Galen, et al.
Human Molecular Genetics
|
May 6, 2016
Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability
Hamid Meziane, Malik Khelfaoui, Noemi Morello, et al.
Biomedicines
|
December 23, 2022
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models
Hamid Meziane, Marie-Christine Birling, Olivia Wendling, et al.
International Journal of Molecular Sciences
|
March 29, 2023
Activation of the PI3K/AKT/mTOR Pathway in Cajal-Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures
Nasim Ramezanidoraki, Driss El Ouardi, Margaux Le, et al.
Human Molecular Genetics
|
November 26, 2015
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
Chloé Delépine, Hamid Meziane, Juliette Nectoux, et al.
Page
of 5