The Coffin-Lowry Syndrome is a rare syndromic form of X-linked intellectual disability. This syndrome is caused by mutations of the Rsk2 gene that encodes a protein kinase, RSK2, in the MAPK/ERK signaling pathway. Characterization of the behavioural phenotype of Rsk2-KO mice mainly showed that they display delayed acquisition and long-term deficits in a spatial reference memory task, suggesting an alteration in hippocampal function. Here, we show that Rsk2-KO mice are also deficient in a learning and memory task that involves dentate gyrus-dependent pattern separation function. Several studies showed the formation of new neurons in the adult dentate gyrus by neurogenesis is a form of plasticity that plays a significant role in hippocampal-d...
Adult hippocampal neurogenesis refers to the creation of neurons during adult life in the dentate gy...
<p>The exact function of the adult brain neurogenesis remains elusive, although it has been suggeste...
Loss of function mutations in the rsk2 gene cause Coffin-Lowry syndrome (CLS), which is associated w...
Le syndrome de Coffin Lowry est une forme syndromique rare de déficience intellectuelle liée au chro...
International audienceAdult neurogenesis is involved in certain hippocampus-dependent cognitive func...
Coffin-Lowry Syndrome (CLS) is an X-linked syndromic form of mental retardation associated with skel...
Les déficiences intellectuelles (DI) affectent 1% de la population mondiale et sont associées à des ...
Coffin-Lowry syndrome is a rare syndromic form of X-linked mental retardation caused by heterogeneous...
Les dernières années témoignent d'une remarquable accélération dans la compréhension des facteurs gé...
Coffin–Lowry Syndrome (CLS), an X-linked form of intellectual disability, is caused by mutations of ...
AbstractCoffin–Lowry Syndrome (CLS) is an X-linked genetic disorder associated with cognitive and be...
Intellectual disability (ID) is a neurodevelopmental disorder associated with impaired cognitive and...
The RSK2 protein is a member of the RSK serine-threonine protein kinase family and is encoded by the...
In adult rodents, decreasing hippocampal neurogenesis experimentally using different approaches ofte...
This work explores the functional role of adult hippocampal neurogenesis in the context of dentate g...
Adult hippocampal neurogenesis refers to the creation of neurons during adult life in the dentate gy...
<p>The exact function of the adult brain neurogenesis remains elusive, although it has been suggeste...
Loss of function mutations in the rsk2 gene cause Coffin-Lowry syndrome (CLS), which is associated w...
Le syndrome de Coffin Lowry est une forme syndromique rare de déficience intellectuelle liée au chro...
International audienceAdult neurogenesis is involved in certain hippocampus-dependent cognitive func...
Coffin-Lowry Syndrome (CLS) is an X-linked syndromic form of mental retardation associated with skel...
Les déficiences intellectuelles (DI) affectent 1% de la population mondiale et sont associées à des ...
Coffin-Lowry syndrome is a rare syndromic form of X-linked mental retardation caused by heterogeneous...
Les dernières années témoignent d'une remarquable accélération dans la compréhension des facteurs gé...
Coffin–Lowry Syndrome (CLS), an X-linked form of intellectual disability, is caused by mutations of ...
AbstractCoffin–Lowry Syndrome (CLS) is an X-linked genetic disorder associated with cognitive and be...
Intellectual disability (ID) is a neurodevelopmental disorder associated with impaired cognitive and...
The RSK2 protein is a member of the RSK serine-threonine protein kinase family and is encoded by the...
In adult rodents, decreasing hippocampal neurogenesis experimentally using different approaches ofte...
This work explores the functional role of adult hippocampal neurogenesis in the context of dentate g...
Adult hippocampal neurogenesis refers to the creation of neurons during adult life in the dentate gy...
<p>The exact function of the adult brain neurogenesis remains elusive, although it has been suggeste...
Loss of function mutations in the rsk2 gene cause Coffin-Lowry syndrome (CLS), which is associated w...