In a major medical breakthrough, India has successfully completed its first human gene therapy for severe hemophilia-A using a lentiviral vector, resulting in zero bleeding rates in patients. Hemophilia, a…
Magazines
-
-
A very interesting news article was published on the website of the journal Nature which comments on the whole course of CRISPR genetic modification technology. In this article, all the…
-
The Laboratory of Physiology of the Department of Medicine of the University of Patras led by Professor Stavros Taraviras has published a new paper in the journal EMBO Molecular…
-
A very interesting study showed that treatment with CART cells that target the urokinase plasminogen activator receptor (uPAR), which is associated with aging, improves exercise capacity in normal aging and…
-
CRISPR gives murine brain stem cells a youthful appearance. Disambling a metabolism-related gene restores cells’ capacity to produce new neurons. Using CRISPR gene editing on mice has shown clues to…
-
Scientists at Trinity College Dublin have developed a very promising gene therapy to treat glaucoma, a debilitating eye condition that affects around 80 million people globally and can result in…
-
Two interesting scientific studies, conducted under the leadership of the Professor of School of Medicine of the National and Kapodistrian University of Athens, Dr. Maria Roubelakis, were published in reputable…
-
An interesting correspondence article was published by The Lancet from the University of Erlangen–Nuremberg in Germany in collaboration with the Bavarian Cancer Research Center (BZKF). This article discusses the CAR…
-
We are pleased to present to you the excellent work of Professor Mrs. Helen A. Papadaki* and her distinguished collaborators, in the reputable “Journal of Clinical Medicine” in which they…
-
Once a death sentence, hemophilia may soon have a treatment. A hereditary condition that primarily affects boys is caused by blood clotting failure. After an injury, hemophilia can result in…
Newer Posts