First and Last Name/s of Presenters

Kevin CullinanFollow

Mentor/s

Dr. Alyssa Woronik

Participation Type

Paper Talk

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR) based gene editing has emerged as an invaluable tool for advances in human health. Through the simple design of single-guide RNAs (sgRNAs), CRISPR-associated proteins (Cas) are guided to make edits within genomes with relative ease compared to previous gene editing techniques. The development of this technology has allowed for improved treatment of diseases such as Sickle Cell Anemia and Leber Congenital Amaurosis. Its usage extends further than just disease treatments, as seen by the ability to decrease malaria transmission rates and increase nutritional value in food. Despite justifiable concerns with the possibility of CRISPR making unwanted gene edits, issues of delivery to cells, and ethical implications, the benefits of CRISPR cannot be ignored. With future work being completed in conjunction with the already known feats of the technology, CRISPR gene editing will ultimately revolutionize the landscape of human health.

College and Major available

Biology

Academic Level

Undergraduate student

Location

Session 2: Digital Commons & Martire 251

Start Day/Time

4-23-2025 2:00 PM

End Day/Time

4-23-2025 3:15 PM

Students' Information

Biology, Honors, 2025

Creative Commons License

Creative Commons Attribution-Noncommercial 4.0 License
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License

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Apr 23rd, 2:00 PM Apr 23rd, 3:15 PM

CRISPR-Cas9: Will it Revolutionize the Landscape of Human Health?

Session 2: Digital Commons & Martire 251

Clustered regularly interspaced short palindromic repeats (CRISPR) based gene editing has emerged as an invaluable tool for advances in human health. Through the simple design of single-guide RNAs (sgRNAs), CRISPR-associated proteins (Cas) are guided to make edits within genomes with relative ease compared to previous gene editing techniques. The development of this technology has allowed for improved treatment of diseases such as Sickle Cell Anemia and Leber Congenital Amaurosis. Its usage extends further than just disease treatments, as seen by the ability to decrease malaria transmission rates and increase nutritional value in food. Despite justifiable concerns with the possibility of CRISPR making unwanted gene edits, issues of delivery to cells, and ethical implications, the benefits of CRISPR cannot be ignored. With future work being completed in conjunction with the already known feats of the technology, CRISPR gene editing will ultimately revolutionize the landscape of human health.

 

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