Sanofi SNY announced that the FDA has granted orphan drug designation to its investigational BTK inhibitor, rilzabrutinib, ...

The efforts of these heroes and heroines were funded almost entirely by grants from the federal government: the National Institutes of Health, the U.S. National Science Foundation and others. The ...

Epigenetic changes do not alter the genetic code itself, but by changing how DNA is organized within the cell, epigenetic ...

Doudna's insights on the future of CRISPR in medicine and agriculture, including the barriers that must be overcome to pave ...

Kashmir University Scientists Pioneer India's First CRISPR-Edited Sheep - SKUAST-Kashmir scientists developed Indias first ...

Princeton University awarded honorary degrees to Omar M. Yaghi, Daniel Chee Tsui, Nancy Weiss Malkiel, Joshua ...

KJ Muldoon came into the world with a genetic time bomb ticking inside him.

Biotechnology has emerged as a driving force in transforming healthcare. Over the past few decades, the integration of biology with advanced technology has led to significant breakthroughs. These ...

G ene therapy has always held enormous promise to correct genetic diseases, but turning that potential into treatments has been challenging.

The one-off treatment highlights the promise of a new type of gene editing and the challenges of using it to treat extremely rare genetic diseases.

‘A revolutionary step in treating #sickle_cell_disease! #CRISPR gene editing is being ... causing blockages, anemia, pain, organ failure, and a significantly shortened lifespan.

These malformed cells get stuck in blood vessels, causing blockages, anemia, pain, organ failure and a ... “This therapy is intended to eliminate sickle cell disease by applying CRISPR technology that ...