One of the key challenges of the modern genomics era is studying the thousands of genes in a single human cell at scale. To ...

CRISPR is a technology that can be used to edit genes and, as such, will likely change the world. The essence of CRISPR is simple: it’s a way of finding a specific bit of DNA inside a cell.

Researchers from Tel Aviv University utilized CRISPR to cut a single gene from cancer cells of head and neck tumors—and successfully eliminated 50% of the tumors in model animals. This study was led ...

A detailed look at the predicted structure of a new CRISPR-Cas tool that promises to expand the genomic editing and manipulating abilities of the original. Researchers at Duke University and North ...

Using gene editing with CRISPR-Cas9, the team has been able to study these proteins without altering ... Dec. 13, 2024 — Microorganisms produce a wide variety of natural products that can be ...

A recently identified bacterial protein structure is contributing to the design of novel anticancer drug delivery systems.

They note that CRISPR systems can only be directed to segments ... They have determined the molecular structure of one of the Tas proteins they found to work in human cells, and will use that ...

Doctors harvest stem cells from the patient’s bone marrow and then send them off to a lab, where CRISPR is used to turn up the production of another, functional version of haemoglobin.

CRISPR technology has revolutionized genetic testing and disease detection, offering precise, rapid, and cost-effective diagnostic solutions. This gene-editing tool has been adapted for molecular ...

The San Francisco-based company housed a cell-specific in vivo gene editing platform that was designed to have a similar structure to an antibody-drug conjugate but with a CRISPR-Cas payload.