Liver cells are indispensable for research—for drug testing, to better understand diseases such as hepatitis, fatty liver, ...
In a first for adults in Singapore, scientists are conducting gene editing trials on heart patients to correct defects at ...
Advances in cancer immunotherapy from immune checkpoint modulation to adoptive cell transfer of tumour-infiltrating ...
The goal of gene therapy is to permanently cure hereditary diseases. One of the most promising technologies for this is the ...
A research team has established a CRISPR/Cas9 gene-editing system for Chrysanthemum morifolium, targeting the CmPDS gene to explore gene functions and enhance breeding. By combining transient and ...
The Food and Drug Administration (FDA) approved the gene therapy Casgevy in December, which uses CRISPR/Cas9 genome editing technology to treat sickle-cell disease (SCD) in patients twelve years and ...
Clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins are core components of fast-evolving therapeutic gene editing tools. Scientists have used CRISPR ...
The news for the chocolate industry is a welcome development, as businesses and scientists grapple with crop shortages.
Like the human immune system, bacteria learn from past infections. CRISPR sequences—short snippets of DNA from previous viruses—guide destructive enzymes towards invading bacteriophages that express ...
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