Скачать или смотреть Rare Genetic Disorder Gene Critical for Intestinal Stem Cell Regeneration | EPFL Study

Discover how a gene linked to Hyaline Fibromatosis Syndrome (HFS) plays a vital role in intestinal stem cell regeneration. EPFL researchers reveal that the CMG2 gene is essential for gut repair after injury, shedding light on rare genetic disorders and advancing regenerative medicine. Learn about Wnt signaling, stem cell biology, and implications for inflammatory bowel disease. This groundbreaking study explains why HFS patients suffer from life-threatening diarrhea and how this discovery could transform gut repair therapies.

Keywords: Hyaline Fibromatosis Syndrome, CMG2 gene, intestinal stem cell regeneration, Wnt signaling, rare genetic disorder, EPFL research, regenerative medicine, gut healing, stem cell biology, inflammatory bowel disease.