Can we fix errors in our genetic blueprint that lead to debilitating disorders like Huntington's disease?How can we better support newcomers to Canada ...

Along with researchers in the Faculty of Health Sciences and the Faculty of Science, Western projects received a total of $17 ...

This study presents a valuable finding on the alterations in the autophagic-lysosomal pathway in a Huntington's disease model. The evidence supporting the claims of the authors is solid. However, the ...

The HDBuzz team caught up with editor emeritus and Huntington's disease specialist, Prof Ed Wild to hear his thoughts on what ...

Delve into the increasingly dynamic landscape of ALS treatment development with thirteen companies advancing candidates in ...

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The process of developing the rare disease "Huntington's disease," in which body parts move involuntarily, has been newly uncovered. Domestic researchers have also developed a protein that treats ...

The cell can then translate those mRNA molecules into proteins, which carry out a variety of functions. Scientists have identified an epigenetic mechanism that seems to balance gene expression. One ...

Researchers have made a major breakthrough in our understanding of Huntington's disease. This genetic disorder has long been known to be caused by mutations in the huntingtin gene, which leads to the ...

People who develop Huntington’s disease have an expansion of these CAG repeats, like a genetic stutter. However, some cells are more vulnerable than others to these effects of HD. Even though the CAG ...

Huntington's disease is a hereditary disorder caused by a genetic mutation in the HTT gene, leading to progressive brain cell damage, affecting movement, cognition, and behavior, with no current cure.

For many people, the symptoms of Huntington's disease will not begin to show for ... Professor Hatters said the exact mechanism of how cells were degenerating or dying was still unknown, it ...