Abstract MeCP2 (Methyl CpG binding protein 2) is an intrinsically disordered protein that
binds to methylated genome regions. The protein is a critical transcriptional regulator of the …

In the rapidly evolving field of Alzheimer's Disease (AD) research, the intricate role of
Hydrogen Sulfide (H2S) has garnered critical attention for its diverse involvement in both …

Autism spectrum disorder (ASD) is a neurodevelopmental disability condition arising from a
combination of genetic and environmental factors. Despite the blood-brain barrier (BBB) …

The study of inborn errors of neurotransmission has been mostly focused on monoamine
disorders, GABAergic and glycinergic defects. The study of the glutamatergic synapse using …

Synaptic abnormalities are a hallmark of several neurological diseases, and clarification of
the underlying mechanisms represents a crucial step toward the development of therapeutic …

Rett syndrome (RTT) is a neurodevelopmental disorder that is caused by mutations in melty-
CpG binding protein 2 (MeCP2). MeCP2 is a non-cell type-specific DNA binding protein, and …

Otizm spektrum bozukluğu (OSB), çocukluk döneminde başlayan ve yaygın bir
nörogelişimsel bozukluk olarak kabul edilmektedir. OSB'nin patofizyolojik temelleri henüz …

Autism spectrum disorder (ASD) is a neurodevelopmental disability condition arising from
the combination of genetic and environmental factors. Despite the blood-brain barrier (BBB) …