Modulation of oxidative stress response in neurodevelopment disorders. The case of the Rett syndrome variants: MECP2 and CDKL
Mutations in the human X-linked cyclin dependent kinase like 5 (CDKL5) gene have recently been ident...
Rett syndrome is a severe neurodevelopmental disorder that arises due to a mutation inmethyl-CpG-bin...
Rett syndrome (RS) is a progressive neurodevelopmental disorder with a large impact on society due t...
As MeCP2 acts a multifunctional regulator of gene transcription, knowing the gene mutation is suffic...
Rett syndrome (RTT, MIM 312750) is a rare and orphan progressive neurodevelopmental disorder affecti...
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting...
International audienceThe main cause of Rett syndrome (RTT), a pervasive development disorder almost...
Rett syndrome (RTT) and MECP2 duplication syndrome (MDS) are neurodevelopmental disorders caused by ...
Rett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively females, caus...
An involvement of the immune system has been suggested in Rett syndrome (RTT), a devastating neurode...
AbstractRett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively femal...
Rett syndrome (RS) is an X-linked neurodevelopmental disorder that represents the second cause of me...
The oxidative stress (OS) hypothesis is able to explain several features of Rett syndrome (RTT), a p...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual dis...
Mutations in the human X-linked cyclin dependent kinase like 5 (CDKL5) gene have recently been ident...
Rett syndrome is a severe neurodevelopmental disorder that arises due to a mutation inmethyl-CpG-bin...
Rett syndrome (RS) is a progressive neurodevelopmental disorder with a large impact on society due t...
As MeCP2 acts a multifunctional regulator of gene transcription, knowing the gene mutation is suffic...
Rett syndrome (RTT, MIM 312750) is a rare and orphan progressive neurodevelopmental disorder affecti...
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting...
International audienceThe main cause of Rett syndrome (RTT), a pervasive development disorder almost...
Rett syndrome (RTT) and MECP2 duplication syndrome (MDS) are neurodevelopmental disorders caused by ...
Rett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively females, caus...
An involvement of the immune system has been suggested in Rett syndrome (RTT), a devastating neurode...
AbstractRett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively femal...
Rett syndrome (RS) is an X-linked neurodevelopmental disorder that represents the second cause of me...
The oxidative stress (OS) hypothesis is able to explain several features of Rett syndrome (RTT), a p...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual dis...
Mutations in the human X-linked cyclin dependent kinase like 5 (CDKL5) gene have recently been ident...
Rett syndrome is a severe neurodevelopmental disorder that arises due to a mutation inmethyl-CpG-bin...
Rett syndrome (RS) is a progressive neurodevelopmental disorder with a large impact on society due t...
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