CRISPR technique can target single genes essential for cancer cell survival, toppling the whole structure, says nanomedicine ...

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 ...

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.

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 ...

"These cells co-develop together, just like they would in an actual embryo, and establish that history of being neighbors," ...

Everything came together last year when Alexander Marson, Gurumurthy, and colleagues used Easi-CRISPR to reprogram the structure and function of human T cells without the need for viral vectors 6.

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 ...

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 ...

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

The CRISPR-Cas gene scissors offer a wide range ... of Wulf Blankenfeldt at HZI have joined forces to decipher the structure of the inhibition mechanism more precisely. Using cryo-electron ...

The researchers applied CRISPR gene technology to investigate whether activating ... Gersbach’s work has led to new approaches to studying genome structure and function, programming cell biology and ...