Japan invests $500 million in US AI project Genesis Mission. We analyze the goals, benefits for the parties, and hidden risks of the technological cold war with China. Read the analysis.
Breakdown of three GenUI strategies: from HTML to Tambo. When to apply, pros-cons, comparison. For product managers and designers — implement adaptive interfaces without chaos.
Doctors edited a newborn's liver by assembling therapy for a unique mutation. Learn how CRISPR-pencil is changing regulation and the future of medicine.
Critical analysis of Reqorsa gene therapy results at ASCO-2026: sample of 18 patients, p=0.05, risks for investors and the real situation of Genprex. Read details.
Learn how to replace text prompts with references for precise AI art generation. Comparison of arena.ai models, post-processing pipeline. Save time on projects — read the guide for designers.
Habits reduce the risk of death by 40.7%, while genes only by 13%, scientists have proven. Learn how to offset poor heredity and extend life after 80 years.
Eric Topol proved: there are no longevity genes, and the $85 billion anti-aging market is overvalued. Find out why lifestyle and AI prevention are more important than peptides and cryochambers.
WhiteLab Genomics created AAV vectors with AI that deliver genes to the mouse brain 50 times more efficiently and accumulate less in the liver. Learn about the breakthrough in gene therapy.
Institute of the Siberian Branch of the Russian Academy of Sciences creates therapeutic oligonucleotides — molecules that switch off cancer and HIV genes. The development of phosphorylguanidines promises treatment without side effects. Learn how Russian genetic engineering bypasses Western patents.
Scientists created a photoactivatable system paCas13d with nanoparticles. The technology cured bone necrosis in mice without harming systemic therapy. Learn how IR light controls genes at tissue depth.
Regeneron's Otarmeni restores hearing to normal in 42% of patients. The therapy treats OTOF gene mutations with a single injection. Learn how AAV vector technology has for the first time restored the ability to hear a whisper.
Scientists from Russia are creating the world's first gene therapeutic drug for aging: a RAGE gene blocker and exosomes against sarcopenia. Learn how the state project promises to restore muscles and prolong active life.
Russian scientists are creating the world's first anti-aging drugs: RAGE gene blocker and exosome rejuvenation. The Ministry of Education and Science promises clinical use by 2030. Learn how transplantation of 'young' vesicles restores muscles and why the budget exceeds 2 trillion rubles.
Single-dose CRISPR therapy NTLA-2002 reduced hereditary angioedema attacks by 87% in phase III. Learn how this will change treatment and pave the way to a cure.
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