India's drug regulations have been updated to include advanced treatments like cell, stem cell, gene therapies, and xenografts under centra...

Tech entrepreneur Ben Lamm is spearheading Colossal Biosciences, a company aiming to bring back extinct species like the woolly mammoth thr...

Karnataka's IT/BT department has approved four initiatives totaling over Rs 27 crore to boost innovation across the state. These projects i...

As global oncology races toward next-generation therapies, Avammune Therapeutics is betting on affordable, orally administered immunotherap...

A new gene editing medicine, VERVE-102, offers hope for millions with heart conditions. Eli Lilly's drug showed significant reductions in b...

Extinct animals coming back: Scientists are pursuing de-extinction, aiming to bring back species like the woolly mammoth and bluebuck. The ...

Octopuses possess a unique ability to rewrite their genetic messages. They extensively edit RNA after its creation, altering instructions b...

Hope is on the horizon for Type-1 diabetes patients. New stem cell therapies are showing remarkable progress. These treatments aim to repla...

Alien genes found in human DNA? A new study claims alien DNA may have been inserted into human genes, suggesting possible hybridization. Th...

Cardiologist Dr. Dmitry Yaranov, widely known as @heart_transplant_doc, has outlined what he calls the “crazy future of heart care” in a vi...

A group of experts cautions that the lack of specific rules for genome-edited crops may hurt transparency, while the government says that e...

India is progressing in cell and gene therapy. Research includes treatments for leukemia, hemophilia-A, sickle-cell anemia, and more.

Millionaire Bryan Johnson visited a remote island to extend his life. He spent $20,000 for a treatment that would keep him young forever.

A Chinese scientist, He Jiankui, claimed last year that he had created the world’s first gene-edited babies using Crispr, to make them resi...

CRISPR, short for clustered regularly interspaced short palindromic repeats, was named "2015 Breakthrough of the Year" by the US journal Sc...

Researchers from Duke University in US used CRISPR to treat an adult mouse model of Duchenne muscular dystrophy.

This technology ultimately has applications in gene therapies for genetic disorders such as sickle cell anemia and cystic fibrosis.