
When Trevor Baglin, a hematologist at Addenbrooke's Hospital at Cambridge University had a head injury patient with a much better-than-expected outcome, he did something unusual. He got very curious. more »


Two initiatives from different ends of the drug development spectrum are shining a bright light on nagging weaknesses in translational medicine and the urgent need to improve speed and efficiency in moving early stage discoveries into therapeutic candidates.
Researchers from the University of California at Berkeley have developed a method that allows them to better target gene therapy viral vectors via directed evolution. For now, they have used their method to make a vector that can more easily reach the back of the eye. But in theory, their method, which consists of multiple rounds of mutagenesis for directed evolution, could be used as a general method to develop viruses for tissues that have been challenging to reach with gene therapy.
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- Protein Folds: Simpler than Current, Complex Notions? »
- Mushroom-Shape Cow Antibody May Broaden Therapeutic Reach »
- Neuroblastoma Discovery May Lead to Wider Cancer Treatment »
- Autoimmune Drug Candidate Helps Mice Keep Trim Waists »
- Study Elucidates Interplay in Cancer Cells, Immune System »
- Alzheimer's Plaque Data Don't Hold Up, Behavioral Data Do »
- Sepsis Patients May Need Bigger Immune Response »
- No Working Kinase, but ErbB3 Acquires Oncogenic Mutations »

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