International audienceMutations in Ribosomal s6 kinase 2 (Rsk2) are associated with severe neuronal dysfunction in Coffin-Lowry syndrome (CLS) patients, flies and mice. So far, the mechanisms of how Rsk2 regulates development, maintenance and activity of neurons are not understood. We have investigated the consequences of Rsk2 deficiency in mouse spinal motoneurons. Survival of isolated Rsk2 deficient motoneurons is not reduced, but these cells grow significantly longer neurites. Conversely, overexpression of a constitutively active form of Rsk2 leads to reduced axon growth. Increased axon growth in Rsk2 deficient neurons was accompanied by higher Erk 1/2 phosphorylation, and the knockout phenotype could be rescued by pharmacological inhibi...
G protein-coupled receptors (GPCRs) are essential for normal central CNS function and represent the ...
Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK sig...
In contrast to the adult mammalian central nervous system (CNS), the neurons in the peripheral nervo...
International audienceMutations in Ribosomal s6 kinase 2 (Rsk2) are associated with severe neuronal ...
Loss of function mutations in the rsk2 gene cause Coffin-Lowry syndrome (CLS), which is associated w...
AbstractCoffin–Lowry Syndrome (CLS) is an X-linked genetic disorder associated with cognitive and be...
More than 80 human X-linked genes have been associated with mental retardation and deficits in learn...
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 ...
International audienceAdult neurogenesis is involved in certain hippocampus-dependent cognitive func...
International audienceThe Coffin-Lowry syndrome, a rare syndromic form of X-linked mental retardatio...
Les déficiences intellectuelles (DI) affectent 1% de la population mondiale et sont associées à des ...
Coffin-Lowry Syndrome (CLS) is an X-linked syndromic form of mental retardation associated with skel...
gene is responsible for Coffin-Lowry syndrome, an X-linked dominant genetic disorder causing mental...
Coffin-Lowry syndrome is a rare syndromic form of X-linked mental retardation caused by heterogeneous...
G protein-coupled receptors (GPCRs) are essential for normal central CNS function and represent the ...
Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK sig...
In contrast to the adult mammalian central nervous system (CNS), the neurons in the peripheral nervo...
International audienceMutations in Ribosomal s6 kinase 2 (Rsk2) are associated with severe neuronal ...
Loss of function mutations in the rsk2 gene cause Coffin-Lowry syndrome (CLS), which is associated w...
AbstractCoffin–Lowry Syndrome (CLS) is an X-linked genetic disorder associated with cognitive and be...
More than 80 human X-linked genes have been associated with mental retardation and deficits in learn...
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 ...
International audienceAdult neurogenesis is involved in certain hippocampus-dependent cognitive func...
International audienceThe Coffin-Lowry syndrome, a rare syndromic form of X-linked mental retardatio...
Les déficiences intellectuelles (DI) affectent 1% de la population mondiale et sont associées à des ...
Coffin-Lowry Syndrome (CLS) is an X-linked syndromic form of mental retardation associated with skel...
gene is responsible for Coffin-Lowry syndrome, an X-linked dominant genetic disorder causing mental...
Coffin-Lowry syndrome is a rare syndromic form of X-linked mental retardation caused by heterogeneous...
G protein-coupled receptors (GPCRs) are essential for normal central CNS function and represent the ...
Ribosomal s6 kinase 2 is a growth factor activated serine/threonine kinase and member of the ERK sig...
In contrast to the adult mammalian central nervous system (CNS), the neurons in the peripheral nervo...