The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more ...

Short RNA sequences could be used to target and shut down specific genes. The second generation came along about a dozen years ago, with the discovery of CRISPR, which stands for clustered ...

Stanford researchers introduced affordable gene-editing kits ready for the classroom, aiming to make the field more accessible for high school students.

By creating gene editors not found in nature, or optimizing existing editors, AI can improve the accuracy, effectiveness, and accessibility of gene editing.

ZUG, Switzerland and BOSTON, Jan. 13, 2025 (GLOBE NEWSWIRE) -- CRISPR Therapeutics (Nasdaq: CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious ...

CRISPR Therapeutics' stock decline is likely influenced by Editas Medicine's struggles, but CRISPR remains a distinct and stronger company with a promising long-term outlook. CRISPR's strategic ...

The CEP290 gene is too big to be carried by viral vectors, but using CRISPR its sequence can be edited to restore its normal function, by snipping out a small section. Allergan licensed rights to ...

Long-read sequencing may be a better option for rare disease diagnosis than short-read sequencing, according to a recent study. The findings revealed that long-read sequencing could reduce both the ...