One of the most commonly used gene-delivery methods relies on engineered viruses to insert stretches of genetic material into ...

G ene therapy has always held enormous promise to correct genetic diseases, but turning that potential into treatments has ...

Treatment seems to have been effective, but it is not clear whether such bespoke therapies can be widely applied.

A gene editing drug custom-made for a critically ill baby showed that, for some ultra-rare diseases, it’s possible to design ...

At stake in the ongoing patent dispute over the gene-editing tool are rights to the most important new biotechnology of the ...

The global CRISPR Market, valued at US$2.90 billion in 2024, is forecasted to grow at a robust CAGR of 11.2%, reaching ...

A big breakthrough is being hailed in the world of gene editing, with the first custom-designed treatment using CRISPR technology (NASDAQ:CRSP). The therapy was developed for an infant named KJ Muloon ...

Baby KJ's bleak future is brighter as CRISPR breakthrough paves the way to treat rare genetic disorders.

近日，美国食品药品监督管理局 (FDA） 批准这种基因编辑猪可供人类食用 ，这标志着 CRISPR 技术在食物链中的首次重大商业应用。据世界动物卫生组织统计，仅在美国，蓝耳病每年就给养殖户造成 5.6 亿美元的损失。爱荷华州立大学专家于 2024 ...

Scientists were able to create a bespoke treatment for KJ Muldoon’s rare genetic disorder within six months. It could be a ...

Yesterday, the US Court of Appeals for the Federal Circuit said scientists Jennifer Doudna and Emmanuelle Charpentier will ...

The company has shown its revolutionary technology can deliver life-changing therapies. Now, it's about whether CRISPR ...