CRISPR Breakthrough Could Rewrite Future of Genetic Disease Treatment

A new CRISPR approach can control genes without cutting DNA, opening a safer path for treating genetic diseases. A newly ...
Morning Overview on MSN

New CRISPR leap could transform treatment for genetic diseases

Gene editing has moved from theory to bedside with a speed that would have seemed impossible a decade ago. A new wave of ...
Nature

AI expands the repertoire of CRISPR-associated proteins for genome editing

Despite emerging clinical successes, current genome editors suffer from off-target effects and can trigger unwanted responses from the immune system, limiting their broader therapeutic applications.
Medical Xpress

First-in-human trial of CRISPR gene-editing therapy safely lowers cholesterol and triglycerides

In a 15-patient, Phase 1, first-in-human trial, a one-time CRISPR-Cas9 gene-editing therapy safely reduced LDL cholesterol and triglycerides in people with difficult-to-treat lipid disorders, ...

insitro Validates AI-Enabled POSH Platform in Nature Communications, Bridging Critical Gap in Drug Discovery

AI therapeutics company built on causal biology, today announced the publication of research in Nature Communications validating its POSH (Pooled Optical Screening in Human cells) platform. The study ...
AZoLifeSciences on MSN

CRISPR for Christmas? The year’s biggest gene editing breakthroughs, unwrapped

In 2025, CRISPR advanced gene editing with safe, effective therapies and AI tools, marking a shift towards real-world ...
STAT

At meeting on guardrails for gene editing of human embryos, some call for a dead end

Megan Molteni reports on discoveries from the frontiers of genomic medicine, neuroscience, and reproductive tech. She joined STAT in 2021 after covering health and science at WIRED. You can reach ...