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Researchers at the Max Planck Institute for Evolutionary Anthropology have addressed a longstanding challenge in CRISPR ...
The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.
Genetic defects are exceedingly common, which is not surprising considering just how many cells make up our bodies, including our reproductive cells. While most of these defects have no or only ...
Institute of Pathogenic Microbiology, Guangdong Provincial Center for Disease Control and Prevention, Guangdong Workstation for Emerging Infectious Disease Control and Prevention, Chinese Academy of ...
CRISPR has already proven to be a successful gene therapy. What's stunning is the speed. KJ's mutation was identified within days of his birth. Within weeks, researchers were growing cells in ...
CRISPR/Cas9-mediated gene editing can successfully correct mutations in the ATP7B gene, which cause Wilson disease (WD), according to results presented at the 2025 European Association for the Study ...
As a type of gene therapy — the umbrella term for any gene-based approach to correcting DNA mutations — CRISPR has wide potential to advance medical treatments, from cancer to high cholesterol. In ...
Copyright 2025 The Associated Press. All Rights Reserved. Copyright 2025 The Associated Press. All Rights Reserved. This photo provided by the Children’s Hospital ...
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A baby born with a rare and devastating genetic condition has become the first person ever to be successfully treated with a personalized CRISPR therapy. After receiving three doses of the therapy ...
The applications did not adequately show possession of an operable CRISPR-Cas9 system in eukaryotic cells, even though they described the core components of the technology. As a result ...
Beccy is a custom content producer who holds a PhD in Biological Science, a Master’s in Parasites and Disease Vectors, and a Bachelor’s in Human Biology and Forensic Science.