CRISPR/Cas9 Editing: T Cell Engineering for Immunotherapies
Jul 06, 2021

News

CRISPR/Cas9 Editing: T Cell Engineering for Immunotherapies

Learn about CRISPR/Cas9-based non-viral knockin for T cell engineering and how the Marson lab at UCSF is optimizing these methods to support T cell therapies.

CRISPR/Cas13: Evolving Biomedical Applications
Jun 21, 2021

News

CRISPR/Cas13: Evolving Biomedical Applications

Learn about advances using CRISPR/Cas13 nucleases in viral detection and treatment, including influenza A and SARS-CoV-2.

Single-Stranded DNA for Improved Knockin Efficiency: Animal Model Generation
Mar 17, 2021

Resource

Single-Stranded DNA for Improved Knockin Efficiency: Animal Model Generation

Learn how long stranded DNA (lssDNA) donor templates facilitates knockin CRISPR/Cas9 editing efficiency for animal model generation.

Progressing toward in vivo CRISPR Gene Editing in the Clinic
Mar 11, 2021

News

Progressing toward in vivo CRISPR Gene Editing in the Clinic

Learn how CRISPR/Cas9 gene-editing ex vivo and in vivo approaches are progressing to treat beta-thalassemia, sickle cell disease, Leber congenital amaurosis, and hereditary transthyretin amyloidosis.

Novel CRISPR-based Non-viral Approach for CAR T Cell Generation
Nov 29, 2020

Blog

Novel CRISPR-based Non-viral Approach for CAR T Cell Generation

Novel CRISPR-based Non-viral Approach for CAR T Cell Generation

Overcoming Antibiotic Resistance with CRISPR
Nov 22, 2020

Blog

Overcoming Antibiotic Resistance with CRISPR

Overcoming Antibiotic Resistance with CRISPR

Tips for Improving the Efficiency of CRISPR mediated Knock-in
Nov 12, 2020

Blog

Tips for Improving the Efficiency of CRISPR mediated Knock-in

Learn about strategies to improve the efficiency of CRISPR mediated knock-in of donor DNA templates.

CRISPR/Cas9 Used to Edit Gene Variance in Human Stem cell-derived β cells from a Patient with Monogenic Diabetes and Reverse Preexisting Diabetes in Mice
Nov 01, 2020

News

CRISPR/Cas9 Used to Edit Gene Variance in Human Stem cell-derived β cells from a Patient with Monogenic Diabetes and Reverse Preexisting Diabetes in Mice

CRISPR/Cas9 Used to Edit Gene Variance in Human Stem cell-derived β cells from a Patient with Monogenic Diabetes and Reverse Preexisting Diabetes in Mice

Discovery of CRISPR/Cas Mechanisms and Genome Editing Potential Wins Nobel Prize
Oct 26, 2020

News

Discovery of CRISPR/Cas Mechanisms and Genome Editing Potential Wins Nobel Prize

Learn about Jennifer Doudna and Emmanuelle Charpentier, the 2020 Nobel prize-Chemistry recipients, for elucidating CRISPR/Cas9’s mechanisms in bacterial immunity as well as its potential for genome editing applications.

 Delivering CRISPR/Cas9: Advances and Challenges
Oct 25, 2020

Blog

Delivering CRISPR/Cas9: Advances and Challenges

Learn about CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas delivery and how viral vs non-viral approaches compare.

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