Breakthrough reveals how viruses efficiently pack genetic material
Researchers at San Diego State University and Michigan State University are shedding new light on how viruses meticulously…
Nanostructures boost CRISPR delivery for genetic medicine
With the power to rewrite the genetic code underlying countless diseases, CRISPR holds immense promise to revolutionize medicine.…
Platelets found to mop up DNA fragments and improve early cancer detection
Platelets are probably best known for their role in blood clotting, making scabs and related, if less salubrious,…
Walking faster may protect your bones and prevent fractures
A large UK Biobank study reveals that simply picking up your walking pace could be a powerful, low-cost…
AI model predicts flu vaccine strains more accurately than WHO
A new study shows that artificial intelligence can beat traditional methods in picking flu vaccine strains, offering a…
Landmark study maps mutational landscape of triple-negative breast cancer in African American women
Triple-negative breast cancer (TNBC), the deadliest breast cancer subtype, disproportionately affects African American women – but until now,…
Exploring testosterone’s influence on cardiovascular, metabolic, reproductive, and mental health
For decades, testosterone has been recognized as the primary driver of male reproductive development and secondary sex characteristics.…
Your DNA, Your Privacy: What Really Happens After a Genetic Test?
The Fascinating World of At-Home DNA Tests 🧪 It starts with a small kit arriving at your door.…
Toddler’s survival from rare disease inspires Brave Like Beck Foundation
Alyssa Dapolito  | Brave Like Beck Foundation STUART — Beckham Willett, a local toddler in Stuart, survived an…
New ESC guidelines introduce unified approach to improve myocarditis and pericarditis care
New ESC Guidelines to improve the diagnosis and care of patients with myocarditis and pericarditis, have been published…
Insights into clinical features and genetic variants of Cornelia de Lange syndrome in China
Cornelia de Lange syndrome (CdLS) is a rare genetic disorder with symptoms, including facial anomalies (such as fused…
New mouse models reveal mechanisms of RP59 retinal degeneration
Retinitis pigmentosa retinal degeneration is caused by a family of hereditary mutations in nearly 100 genes that slowly…