hemophilia b वाक्य
"hemophilia b" हिंदी में hemophilia b in a sentenceउदाहरण वाक्य
- A gene therapy treatment for hemophilia B might be of great benefit, he said, and would need to be weighed against the risks, including that of inadvertently modifying the human germ line.
- The trial, conducted by Avigen of Alameda, Calif ., is designed to insert a corrective gene into the liver of patients with hemophilia B, the less common of two forms of hemophilia.
- In January 2007, the company announced it would acquire Syntonix Pharmaceuticals for up to $ 120 million, gaining Syntonix's lead product for hemophilia B as well as the technology for developing inhalable treatments.
- The results, which produced a blood-clotting protein without adverse side effects, were reported in research connected with hemophilia B, which affects about 5, 000 Americans, or 20 percent of all hemophiliacs in America.
- In 2009 genetic analysis determined specifically that he suffered from hemophilia B . He had to be careful not to injure himself because he lacked factor IX, one of the proteins necessary for blood-clotting.
- Hemophilia B is a good target for gene therapy because the level of Factor IX in the bloodstream needs to be raised and sustained at only 1 percent of normal for patients to benefit.
- The trial, conducted by Avigen Inc . of Alameda, Calif ., is designed to insert a corrective gene into the liver of patients with hemophilia B, the less common of two forms of hemophilia.
- Calcium-binding EGF-like domains ( cbEGF-like domains ) play a seminal role in diseases such as the Marfan syndrome or the X-chromosome linked hemorrhagic disorder hemophilia B and are among the most abundant extracellular calcium-binding domains.
- But Nagle said hemophilia B is so rare _ only 150 cases are diagnosed annually _ that seven subjects are probably representative of those in the general population who suffer from this rare bleeding disorder.
- The cause of hemophilia B is decreased activity or deficiency of blood coagulation factor IX . Point mutations resulting in decreased affinity of factor IX to calcium are thought to be implicated in this bleeding disorder.