Most people have never heard of spinal muscular atrophy (SMA), a rare genetic disease that affects approximately 1 in 6,000 babies born worldwide each year. Innovative research may produce treatments for patients suffering from SMA and other rare diseases.

New NIBR President Jay Bradner shares on drug discovery, his leadership style and what’s next for his career in biomedical research.

Novartis taps MOOC technology to share chemistry education with the world

Why are some sickle cell disease patients protected from the disease? Learn about our biomedical research in the field.

Read how nature's medicine chest empowers our drug discovery chemists to advance biomedical research