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Our polygenic score will enable the application of these treatments to people that specifically need it through precision medicine by identifying the individual at high genetic risk of low circulating levels of the vitamin. The answer is no because there are both genetic and dietary (environmental) causes for low vitamin A.
The CCDI Molecular Targets Platform (MTP) is a collaborative effort between the Children’s Hospital of Philadelphia and the Frederick National Laboratory with input from the NCI and the U.S. Clinicians decide on an optimal treatment regimen based on the patient’s cancer subtype. Food and Drug Administration (FDA).
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This enables us to explore novel drug candidates that could be more effective or have fewer side effects than existing treatments and drugs. Mutlu has a robust academic background that includes a bachelor’s degree in physics, a master’s degree in bioengineering, and a PhD in bioinformatics from the University of Cambridge.
The study suggests that this regulatory system could be a potential target for future malaria treatments, offering hope for combatting this deadly disease that affects millions worldwide. With this newfound knowledge, there is renewed hope in the pursuit of effective malaria treatments alleviating the suffering of millions affected.
Study co-senior investigator Dr Aristotelis Tsirigos is a professor in the Departments of Pathology and Medicine at NYU Grossman School of Medicine and Perlmutter Cancer Center, where he also is co-director of precision medicine and director of its Applied BioinformaticsLaboratories.
Founded and led for 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to eight FDA-approved treatments and numerous product candidates in development, all of which were homegrown in our laboratories.
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