Rett Syndrome (RTT) is a severe, rare, and progressive developmental disorder with patients
displaying neurological regression and autism spectrum features. The affected individuals …

Rett Syndrome (RTT) is a rare and progressive neurodevelopmental disorder that is caused
by de novo mutations in the X-linked Methyl CpG binding protein 2 (MECP2) gene and is …

Rett syndrome (RTT) is a severe and rare neurological disorder that is caused by mutations
in the X-linked MECP2 (methyl CpG-binding protein 2) gene. MeCP2 protein is an important …

Eukaryotic gene expression is controlled at multiple levels, including gene transcription and
protein translation initiation. One molecule with key roles in both regulatory mechanisms is …

Rett Syndrome (RTT) is a neurodevelopmental disorder characterized by neurological regression
and autism spectrum features, usually in females with mutation in MECP2. Animal and …

The COVID-19 pandemic has had a significant impact on medical services. Many countries
postponed nonemergent procedures to preserve hospital resources for the unprecedented …

Interval-training activities induce adaptive cellular changes without altering their fundamental
identity, but the precise underlying molecular mechanisms are not fully understood. In this …

A28-year-old, otherwise healthy female was referred to the neurology clinic after having 3
generalized tonic–clonic seizures over 3 days. Neurologic and general medical examinations …

Background and Purpose Erb-B1 (epidermal growth factor receptor, EGFR) and Erb-B2 (HER-2)
are two of the best-characterized members in the EGFR pathway. In many tumor types, …

Common variable immunodeficiency syndrome (CVID) includes a heterogeneous disorder
characterized by reduced levels of IgG, IgA or IgM, and recurrent bacterial infections with …