Two new studies reveal novel DNA-binding properties of MeCP2, mutations of which cause Rett syndrome. Baker et al. report critical roles for the AT-hook domain of MeCP2 in chromatin organization and clinical features of Rett syndrome. Mellén et al. find the methyl-CpG-binding domain of MeCP2 interacts with hydroxymethyl-CpG
Rett syndrome is a human intellectual disability disorder that is associated with mutations in the X...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...
SummaryMutations in the X-linked MECP2 cause Rett syndrome, a devastating neurological disorder typi...
Two new studies reveal novel DNA-binding properties of MeCP2, mutations of which cause Rett syndrome...
Methyl-CpG binding protein 2 (MeCP2) is a multifunctional epigenetic reader playing a role in transc...
Methyl-CpG binding protein 2 (MeCP2) is a multifunctional epigenetic reader playing a role in transc...
Methyl-CpG binding protein 2 (MeCP2) is a multifunctional epigenetic reader playing a role in transc...
SummaryMutations in the X-linked MECP2 cause Rett syndrome, a devastating neurological disorder typi...
Genetic mutations of the X-linked gene MECP2, encoding methyl-CpG-binding protein 2, cause Rett synd...
The importance of DNA methylation in neuronal function is highlighted by mutations in the neuronally...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...
The importance of DNA methylation in neuronal function is highlighted by mutations in the neuronally...
Background: Rett syndrome (RTT) is a complex neurological disorder that is one of the most frequent ...
MeCP2 was initially identified as an abundant protein in the brain, with an affinity for methylated ...
Rett syndrome is a human intellectual disability disorder that is associated with mutations in the X...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...
SummaryMutations in the X-linked MECP2 cause Rett syndrome, a devastating neurological disorder typi...
Two new studies reveal novel DNA-binding properties of MeCP2, mutations of which cause Rett syndrome...
Methyl-CpG binding protein 2 (MeCP2) is a multifunctional epigenetic reader playing a role in transc...
Methyl-CpG binding protein 2 (MeCP2) is a multifunctional epigenetic reader playing a role in transc...
Methyl-CpG binding protein 2 (MeCP2) is a multifunctional epigenetic reader playing a role in transc...
SummaryMutations in the X-linked MECP2 cause Rett syndrome, a devastating neurological disorder typi...
Genetic mutations of the X-linked gene MECP2, encoding methyl-CpG-binding protein 2, cause Rett synd...
The importance of DNA methylation in neuronal function is highlighted by mutations in the neuronally...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...
The importance of DNA methylation in neuronal function is highlighted by mutations in the neuronally...
Background: Rett syndrome (RTT) is a complex neurological disorder that is one of the most frequent ...
MeCP2 was initially identified as an abundant protein in the brain, with an affinity for methylated ...
Rett syndrome is a human intellectual disability disorder that is associated with mutations in the X...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (ID...