Huntington's disease (HD) is a progressive neurodegenerative disease characterized by
preferential loss of neurons in the striatum in patients, which leads to motor and cognitive …

Oligodendrocytes (OLs) are a major type of glial cells in the central nervous system that
generate multiple myelin sheaths to wrap axons. Myelin ensures fast and efficient …

Huntington's disease (HD) is an autosomal-dominant inherited progressive
neurodegenerative disorder. It is caused by a CAG repeat expansion in the Huntingtin gene …

Background Sepsis-associated encephalopathy (SAE) is an acute cerebral dysfunction
caused by sepsis. Neuroinflammation induced by sepsis is considered a potential …

Huntington disease (HD) is a fatal neurodegenerative disorder caused by an expanded
CAG repeat in the huntingtin (HTT) gene. The typical motor symptoms have been associated …

Pathogenesis of the inherited neurodegenerative disorder Huntington's disease (HD) is
progressive with a long presymptomatic phase in which subtle changes occur up to 15 years …

Introduction Huntington's disease (HD) is caused by expanded CAG repeats in the
huntingtin gene (HTT) and is characterized by late-onset neurodegeneration that primarily …

Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder that
occurs with the increase of CAG trinucleotide repeats in the huntingtin gene. To understand …

Multiple sclerosis (MS) is the main reason for disability caused by autoimmunity. However,
effective biomarkers for MS have not been identified. This study explored the molecular …

Magnoflorine (Mag), a natural alkaloid component originating from the Ranunculaceae Juss.
Family, has a various of pharmacological activities. This study aimed to investigate the …