Fintel reports that on February 3, 2025, HC Wainwright & Co. initiated coverage of CRISPR Therapeutics (NasdaqGM:CRSP) with a ...
Potent in vivo gene editing in skeletal muscle of non-human primates by a novel, ultracompact CRISPR system delivered via a single AAV vector.
H.C. Wainwright analyst Mitchell Kapoor initiated coverage of Crispr Therapeutics (CRSP) with a Buy rating and $65 price target The firm says ...
Precision medicine is revolutionizing healthcare, and these genomic stocks are leading the way. Therefore, as this sector ...
The innovation, he says, could transform the way scientists measure and address genomic breaks in gene-editing systems.
By creating gene editors not found in nature, or optimizing existing editors, AI can improve the accuracy, effectiveness, and accessibility of gene editing.
What makes the perfect human? Immaculate features? Indomitable Intelligence? Incomparable wit? Or irresistible charm? What if ...
Overnight DeepSeek is the role model of the startup ecosystem. It is demonstrating real-time to every business, idea, or ...
The U.S. Food and Drug Administration (FDA has cleared the investigational new drug (IND) application for Allogene Therapeutics’ ALLO-329, an investigational allogenic CAR-T cell therapy.
One sickle cell patient told ITV News the new gene therapy being rolled out for use on the NHS means they "finally have something to look towards". | ITV National News ...
Encasing CRISPR tools in oil droplets offers a fast-track approach to conducting extensive genetic screens in animals.
Both Cas9 and Cas12a cleave DNA, but they differ in how they cut the molecule.