CRISPR-Cas9 genome editing exploits the CRISPR ... Cytosine base editing is crucial for modeling human diseases in zebrafish. Here, the authors present zevoCDA1 and zevoCDA1-198, optimized editors ...

Genes contain instructions for making proteins, and a central dogma of biology is that this information flows from DNA to RNA ...

For the past decade, scientists have relied almost exclusively on CRISPR-Cas systems for genome editing. Now, a smaller but ...

Beyond Needles: Introducing a New, Nature-Based Approach ... Like Virus from Genomes of Non-Human Primates Aug. 17, 2023 — A single injection of a novel CRISPR gene-editing treatment safely ...

Labroots invites you to the 7th Annual Event in the CRISPR Virtual Event Series 2024 taking place on October 23rd, 2024! This event will continue the conversation of the abilities of CRISPR-based ...

Researchers have developed a novel delivery system for sending CRISPR reagents to brain cells, where it performs its gene ...

A single treatment with a CRISPR-Cas9 based gene editing therapy is enough to replace the daily medication of patients with hereditary angioedema (HAE), a condition characterized by severe ...

CASGEVY™ approved for the treatment of patients 12 years of age and older with sickle cell disease (SCD) and transfusion-dependent beta ...

HuidaGene Therapeutics gets US FDA clearance for CRISPR/Cas13 RNA-editing HG202 for macular degeneration: Shanghai Tuesday, November 5, 2024, 09:00 Hrs [IST] HuidaGene Therapeutic ...