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We Stand in Solidarity Against Racism

The Department of Bioengineering stands in solidarity with our students, staff and faculty against social injustice and acts of racism. We are shocked and saddened by the recent, brutal deaths of George Floyd, Ahmaud Arbery, Breonna Taylor, Nina Pop, Rayshard Brooks and others. Like many members of our community, we are frustrated that these deaths are only the most recent manifestations of long-standing racial inequality in this country. 
The Department supports the call to action made by the Bourns College of Engineering.
•    We acknowledge that systemic racism permeates and poisons all levels of academia. 
•    We affirm that the Department has zero tolerance for racism, institutional bias or acts of violence against Black members of our community. 
•    We are committed to supporting Black students and combating the bias and inequity they face. 
•    We are committed to critically examining our recruitment and retention efforts to better support Black students, faculty and staff. 
We would also like to take this moment to recognize the essential contributions made every day by Black students, faculty and staff. They are part of the Bioengineering family, and the department would not be as strong today without their efforts.


Colloquium Speaker: Joshua Wood

Winston Chung Hall 205/206

Title: Efficient generation and phenotyping of genome- edited rodent models using CRISPR-Cas9 in a high throughput pipeline


Abstract: The emergence of CRISPR-based endonuclease technology represents a paradigm shift in our approach to generating animal models that precisely recapitulate human disease. CRISPR-Cas9 has enabled a wide range of mutation types, including genetic knockouts, knockins of humanized alleles (SNPs), conditional/reporter genes, etc. The primary mission of the Mouse Biology Program (MBP) is to enable and facilitate in vivo functional modeling of human disease in mice and other species. To this end we conduct cutting edge research to increase the precision and efficiency of genetic engineering in vivo. We have pioneered high-throughput electroporation of zygotes and other methods that are 4-fold more efficient for producing deletion and SNP mutant models and 3 fold more efficient in the generation of conditional and reporter mice. We have applied these improvements to create a high throughput production pipeline that generates more than 200 unique mouse models per year. Through the Knock-Out Mouse Project (KOMP), we offer a unique opportunity to generate new models at no or little cost to investigators. Unique to MBP is not only our ability to generate mouse models but also the breadth and depth with which we can assess and measure phenotype. This capability has led us to conduct innovative research in cancer, autism, leukemia, musculoskeletal disorders, ocular diseases, deafness, and a host of other diseases and disorders.

Biography: As the associate director for operations in the UC Davis Mouse Biology Program. Dr. Wood leads the Genetic Engineering, Stem Cell, Transgenic Technologies, and In Vitro Fertilization & Cryopreservation Laboratories.  Dr. Wood’s research goals are to develop novel precision medicine models and technologies that advance genetic engineering with innovative approaches to treating diseases and disorders with specific research missions in cancer biology, immune mediated diseases and disorders as well as ophthalmology. The combination of his private and industry experience with his PhD and MBA provide a unique perspective on research and ongoing process improvement in the production and phenotyping of animal models.

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