News for Healthier Living
Gene Therapy May Slow Loss of Motor Function in ALS, Penn and CHOP Research Finds
Researchers have developed a gene therapy that significantly slowed motor function loss in preclinical models of amyotrophic lateral sclerosis (ALS), offering new hope for treating the devastating neurodegenerative disease. "Silencing" a gene associated with regulating TDP-43, the protein that accumulates in the brain and causes ALS, with a technique called RNA interference (RNAi) allowed mice to survive an average of 54 percent longer. Subjects also experienced improvements in strength and reduced inflammation in the brain and spinal cord, according to research from the Perelman School of Medicine at the University of Pennsylvania and Children's Hospital of Philadelphia, published today in Nature Communications.
June 25, 2025
June 25 2025June 24 2025June 23 2025June 22 2025June 21 2025June 20 2025June 19 2025June 18 2025 - Consensus Statement on Universal Chemosensory Testing Calls for Better Standardization, Infrastructure, and Education in the Field
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