There are a range of skills agritech professionals should aim to brush up on for a long-lived career in the sector.

The global Cancer Gene Therapy Market was valued at US$ 3.89 billion in 2024 and is projected to experience a remarkable surge to US$ 17.57 billion by 2033, growing at a compelling CAGR of 18.24% ...

“For example, cell wall engineering can improve protein secretion and simplify downstream processing, while precise gene integration and genome editing tools like CRISPR-Cas9 can ensure ...

Suffering on such an immense scale can appear hopeless. However, a technique called CRISPR gene editing promises to help deal with these issues and many more—and wise regulation can spur it on.

Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein (CRISPR/Cas) technologies have evolved rapidly over the past decade with the continuous discovery of new Cas systems ...

This month's cover highlights the article Immune cells adapt to confined environments in vivo to optimise nuclear plasticity for migration by Helen Weavers and Tua Karling. The cover features confocal ...

Watch:2020 Chemistry Nobel for developing CRISPR/Cas9 genetic scissors The CRISPR ... The gene encoding the CAR is synthesised in the lab, and a vector — often a viral vector, is used to deliver ...

At the heart of this technology is the Cas9 protein, often likened to molecular ... where analytical chemistry and life science collide, CRISPR’s growing influence is unmistakable, taking ...

A proof-of-concept study shows that CRISPR-Cas9 can eliminate extra chromosome copies in Down syndrome cells. The method restores normal gene function but is not yet ready for human trials. Scientists ...

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.

8 Advent and advancements in gene editing tools and cell therapy approaches, including autologous chimeric antigen receptor (CAR) T cell therapy, CRISPR-Cas9, and viral vector engineering ...

The decision has ushered in a new era for sickle cell disease treatment — and marked the world’s first approval of a medicine based on CRISPR/Cas9 gene-editing technology. A foundation for the first ...