Roberta Russo
99 posts
This paper reveals how dual inheritance of SEC23B and PIEZO1 pathogenic variants amplifies erythropoietic stress and ferritin accumulation. The authors provide evidence that multi‑locus genetics can significantly alter disease outcomes. Go in depth 👉bit.ly/3NOkP2Y
The Sant Pau's Research Institute is hosting a new seminar on the genetic landscape of hereditary red blood cells and iron metabolism disorders🧬 🔬Understanding the genetic mechanisms underlying these hereditary conditions remains a major scientific challenge, one that requires continuous research and multidisciplinary collaboration. Advances in genomic technologies have led to the discovery of numerous genetic variants, yet their functional interpretation and clinical correlation are still evolving. 🌟We will have the participation of Professors Roberta Russo and Immacolata Andolfo, internationally recognised for their scientific contributions in the molecular basis of erythropoiesis and iron regulation. ℹ️Don't miss this oportunity and join us to explore the latest breakthroughs in this field👇🏽 docs.google.com/forms/d/e/1FAI… #TogetherWeResearch
🔜#NEXT Week don't miss the #ThursdayWebinar on "Connection between PIEZO1, dehydrated hereditary stomatocytosis, and iron overload", provided by @ImmaAndolfo. 📆23 May - 17h Register now!👉 bit.ly/3KbQDJX #ThursdayWebinar #ERNeu #ERNs #HealthUnion #EU4Health
