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Hugo Bellen, DVM, PhD
Professor
Departments of Molecular & Human Genetics and Neuroscience
Baylor College of Medicine

February 24 @ 12:00 pm - 1:00 pm

presents, “Tackling human gene function in model organisms”

Hosted by: Dr. Tim Schedl

Seminar abstract:  It is estimated that there are more than 300 million patients worldwide with a rare genetic disease. Many of these patients remain undiagnosed for many years. By sequencing their genomes and those of their relatives, human geneticists can now discover genetic variations that are rare or ultra-rare. However, considering that there are many polymorphisms in the population, assessing which variant(s) is/are related to the observed symptoms remains a significant challenge. This is precisely where model organisms can contribute and Drosophila is now playing a prominent role in the discovery of rare human genetic diseases as part of the Undiagnosed Diseases Network and based on collaborations with human geneticists around the world. I will show how we participate in the discovery of new human diseases, the technologies that allow us to do so, how we work out the pathogenic mechanisms, and how we screen existing drugs for therapeutic purposes.

Zoom webinar link: https://wustl-hipaa.zoom.us/j/94367220300

Details

Date:
February 24
Time:
12:00 pm - 1:00 pm
Event Category:

Organizer

Tim Schedl
Phone:
314.362.7855
Email:
ts@wustl.edu