Her parents encouraged her to partake in a trial for a CRISPR -based therapy for sickle-cell disease and beta-thalassemia, another debilitating genetic blood disorder. The therapy, Casgevy, was made ...

CRISPR places an entirely new kind of power into human hands. For the first time, scientists can quickly and precisely alter, delete, and rearrange the DNA of nearly any living organism ...

The CRISPR-led gene-editing revolution is set to begin next month in its first ever trial in humans. The small phase 1 trial, to take place in China, will be investigating the method’s safety ...

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

自从基因编辑策略CRISPR出现以来，它遇到了一个很大的限制：经典的CRISPR系统太笨重了，无法进入人体的许多组织并进行切片和切割。现在，加州大学伯克利分校的Jennifer Doudna因帮助开发CRISPR而获得2020年诺贝尔奖，她与人共同创立了一家公司，该公司的研究人员 ...

Scientists have found a way to study early embryonic development without real embryos. Using CRISPR, they programmed stem cells to self-organize into structures mimicking early embryos. The cells show ...

CRISPR-Cas9 genome editing exploits the CRISPR ... integration of a large transgene to a safe-harbor site in the human genome. Retinitis pigmentosa (RP) is the most common type of inherited ...

Scientists used CRISPR technology to create embryo-like structures, or embryoids, from stem cells. These programmable models ...

India has the chance to lead in CRISPR technology by driving ethical gene editing innovations in healthcare, agriculture, and ...

But only two percent of the human genome actually encodes ... Nov. 6, 2024 — The CRISPR tool is capable of repairing the genetic defect responsible for the immune disease chronic granulomatous ...

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.