Protein linked to ALS/Ataxia could play key role in other ne

Protein linked to ALS/Ataxia could play key role in other neurodegenerative disorders


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Neurological disorders are the number one cause of disability in the world, leading to seven million deaths each year. Yet few treatments exist for these diseases, which progressively diminish a person's ability to move and think.
Now, a new study suggests that some of these neurological disorders share a common underlying thread. Staufen1, a protein that accumulates in the brains of patients with certain neurological conditions, is linked to amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease, along with other neurological disorders, including Alzheimer's, Parkinson's, and Huntington's disease, according to University of Utah Health scientists.
The findings connect Staufen1 to the emerging concept that neurodegenerative diseases are linked to malfunctions in the way cells cope with cellular stress. These results, based on laboratory studies of human tissue and mouse models, suggest that targeting Staufen1 could eventually lead to therapeutic interventions for a number of these disorders.

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, Karlap Figueroa , Lou Gehrig , Warunee Dansithong , Stefan Pulst , Mandi Gandelman , Daniel Scoles , Sharan Paul , University Of Utah School Medicine , National Institute Of Neurological , Nu Health , Harrington Discovery Institute , University Of Utah Health , Department Of Neurology , Utah Health , Utah School , Human Neurodegeneration , National Institute , லூ கேஹ்ரிக் , ஷரன் பால் , பல்கலைக்கழகம் ஆஃப் உட்டா பள்ளி மருந்து , தேசிய நிறுவனம் ஆஃப் நரம்பியல் , உ ஆரோக்கியம் , ஹாரிங்டன் கண்டுபிடிப்பு நிறுவனம் , பல்கலைக்கழகம் ஆஃப் உட்டா ஆரோக்கியம் , துறை ஆஃப் நரம்பியல் , உட்டா ஆரோக்கியம் , உட்டா பள்ளி , தேசிய நிறுவனம் ,

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