display a defect in the nucleotide excision repair pathway, four (Huntington's disease, various spinocerebellar ataxias, Friedreich's ataxia and myotonic dystrophy types 1 and 2) exhibit an ...

Korah leads a rebellion against Moses and Aaron; plague sent by God; Aaron’s rod; duties for priests; the tithe offering Korah, Dathan, and Abiram rose up before Moses, with certain of the children of ...

A new discovery offers hope for Huntington’s disease. This discovery provides hope that a DNA repair process may help slow or ...

Several neuropsychiatric disorders such as attention deficit-hyperactivity disorder (ADHD), autism spectrum disorder (ASD), as well as neurological diseases such as spinocerebellar ataxia type 3 (SCA3 ...

According to Biohaven, the FDA’s decision on the NDA is expected during the 3rd quarter of 2025. The Food and Drug Administration (FDA) has accepted for Priority Review the New Drug Application ...

Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder caused by expansion of a polyglutamine tract in ataxin-1. In affected neurons of SCA1 patients and ...

When we interact with the environment around us, we are sometimes active participants, making directed physical motor movements and other times only mentally engaging with our environment, taking in ...

Labroots is thrilled to announce the 13th Annual Event in the Neuroscience Virtual Event Series, streaming live on March 5th, 2025. Join us as we dive into the captivating world of neuroscience, ...

Suggested remit: To appraise the clinical and cost effectiveness of Troriluzole within its marketing authorisation for treating ataxia.