Trinucleotide expansions cause disease by both protein- and RNA-mediated mechanisms.
Unexpectedly, we discovered that CAG expansion constructs express homopolymeric …

This study investigates the critical elements of parent involvement as related to children's
improved academic achievement. Survey data were collected from 220 parents whose children …

Neuronal atrophy in neurodegenerative diseases is commonly viewed as an early event in
a continuum that ultimately results in neuronal loss. In a mouse model of the polyglutamine …

SCA1, a fatal neurodegenerative disorder, is caused by a CAG expansion encoding a
polyglutamine stretch in the protein ATXN1. We used RNA sequencing to profile cerebellar gene …

Spinocerebellar ataxia type 1 (SCA1) is an incurable, dominantly inherited neurodegenerative
disease of the cerebellum caused by a polyglutamine-repeat expansion in the protein …

In the present study, we investigated remote laser-induced fluorescence (LIF), at a distance
of 4.8m, of a variety of natural minerals and rocks, and Hawaiian Ti (Cordyline terminalis) …

Previous studies indicate that while transgenic mice with ATXN1[30Q]-D776-induced disease
share pathological features caused by ATXN1[82Q] having an expanded polyglutamine …

Mitochondrial dysfunction plays a significant role in neurodegenerative disease including
ataxias and other movement disorders, particularly those marked by progressive degeneration …

Nationwide, agricultural education has experienced a shortage of qualified school-based
agriculture teachers for over four decades. Students who seek careers as agriculture teachers …

Spinocerebellar ataxias (SCAs) are a group of genetic diseases characterized by progressive
ataxia and neurodegeneration, often in cerebellar Purkinje neurons. A SCA1 mouse model…