Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK signaling pathway. Mutations in the Rsk2 gene cause Coffin-Lowry syndrome, a rare syndromic form of intellectual disability. The Rsk2 KO mouse model was shown to have learning and memory defects. We focused on the investigation of the emotional behavioral phenotype of Rsk2 KO mice mainly in the IntelliCage. They exhibited an anti-depressive, sucrose reward seeking phenotype and showed reduced anxiety. Spontaneous activity was increased in some conventional tests. However, KO mice did not show defects in place learning, working memory and motor impulsivity. In addition, we found changes of the monoaminergic system in HPLC and qRT-PCR experiments....
In the last years, RNA interference (RNAi)-mediated gene knockdown has developed into a routine meth...
The economic burden associated with major depressive disorder and anxiety disorders render both diso...
Intellectual disability (ID) is a neurodevelopmental disorder associated with impaired cognitive and...
Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK sig...
Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK sig...
Coffin-Lowry syndrome is a rare syndromic form of X-linked mental retardation caused by heterogeneous...
Loss of function mutations in the rsk2 gene cause Coffin-Lowry syndrome (CLS), which is associated w...
International audienceThe Coffin-Lowry syndrome, a rare syndromic form of X-linked mental retardatio...
RSK2 is a Ser/Thr kinase acting in the Ras/MAPK pathway. Rsk2 gene deficiency leads to the Coffin-Lo...
Coffin-Lowry Syndrome (CLS) is an X-linked syndromic form of mental retardation associated with skel...
The RSK2 protein is a member of the RSK serine-threonine protein kinase family and is encoded by the...
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...
International audienceMutations in Ribosomal s6 kinase 2 (Rsk2) are associated with severe neuronal ...
In recent years, the ERK/MAPK signalling pathway has been implicated into emotional behaviour and th...
In the last years, RNA interference (RNAi)-mediated gene knockdown has developed into a routine meth...
The economic burden associated with major depressive disorder and anxiety disorders render both diso...
Intellectual disability (ID) is a neurodevelopmental disorder associated with impaired cognitive and...
Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK sig...
Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK sig...
Coffin-Lowry syndrome is a rare syndromic form of X-linked mental retardation caused by heterogeneous...
Loss of function mutations in the rsk2 gene cause Coffin-Lowry syndrome (CLS), which is associated w...
International audienceThe Coffin-Lowry syndrome, a rare syndromic form of X-linked mental retardatio...
RSK2 is a Ser/Thr kinase acting in the Ras/MAPK pathway. Rsk2 gene deficiency leads to the Coffin-Lo...
Coffin-Lowry Syndrome (CLS) is an X-linked syndromic form of mental retardation associated with skel...
The RSK2 protein is a member of the RSK serine-threonine protein kinase family and is encoded by the...
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...
International audienceMutations in Ribosomal s6 kinase 2 (Rsk2) are associated with severe neuronal ...
In recent years, the ERK/MAPK signalling pathway has been implicated into emotional behaviour and th...
In the last years, RNA interference (RNAi)-mediated gene knockdown has developed into a routine meth...
The economic burden associated with major depressive disorder and anxiety disorders render both diso...
Intellectual disability (ID) is a neurodevelopmental disorder associated with impaired cognitive and...