Blocking Hedgehog Pathway Could Restore Perfect Corneal Healing After Eye Injuries
Scientists discover how to reverse scarring that prevents clear vision recovery after corneal damage.
Stem cells, exosomes, gene therapy, peptides, hyperbaric oxygen, and epigenetic reprogramming
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Scientists discover how to reverse scarring that prevents clear vision recovery after corneal damage.
New tissue-engineered heart conduit could restore normal circulation in children with congenital heart defects, potentially extending lifespans.
New research identifies a drug target that could help millions of fractures heal properly when blood flow is compromised.
Enhanced stem cells reduced inflammation and improved bladder function in rats with nerve damage.
Researchers demonstrate that transplanting healthy lung cells can repair damaged lungs in mice with genetic disease.
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.