Stem cells, exosomes, gene therapy, peptides, hyperbaric oxygen, and epigenetic reprogramming
421 articles
New research reveals tissue-specific barriers to AAV9 gene therapy effectiveness, particularly in liver cells of primates.
Scientists discover how to make gene therapy work even when patients have prior immune exposure to treatment vectors.
Researchers develop innovative method to guide immune cells to pancreatic tumors using engineered viruses and targeted cytokines.
Scientists develop a $70 gene editing platform that could democratize CRISPR therapy for blood disorders and aging-related diseases.
New gene therapy vectors using baboon virus envelopes outperform human versions for delivering genes to T cells, B cells, and stem cells.
Complex patent laws and regulations are limiting global access to life-saving CRISPR gene therapies.
Scientists discover breakthrough approach to treating the emotional suffering component of chronic pain, offering new hope for millions.
New biotechnology breakthrough enables cells to store mRNA data for later retrieval, opening possibilities for advanced health monitoring.
Groundbreaking cellular therapy gets green light for human testing, potentially reversing aging at the cellular level.
Revolutionary AI tool can forecast disease onset years in advance, potentially transforming preventive healthcare and longevity strategies.
New research reveals how muscle stem cells fine-tune their activation through alternative RNA splicing mechanisms.
Scientists used human brain cells on microchips to decode how genetic mutations lead to ataxia, migraines, and epilepsy.
