RNA-based control switch could be used to turn on gene therapies in cells
A new technique to turn therapeutic genes on in specific cells has been developed, potentially changing the future of gene therapies...
Unintended changes to a genome, away from the desired target site, which occur as a consequence of genome editing.
A new technique to turn therapeutic genes on in specific cells has been developed, potentially changing the future of gene therapies...
In-depth mapping of DNA repair mechanisms of the double-stranded and single-stranded breaks required for genome editing, could enhance the efficacy of these approaches, new research has revealed...
Base editing, a form of genome editing, has been used in preclinical model to correct a lysosomal storage disease known as Hurler syndrome...
Using CRISPR/Cas9 genome editing in human embryos may introduce 'on-target' errors...
A type of genome editing had been used in mice to treat the symptoms of progeria, a fatal premature ageing disease in children...
CRISPR-based genome editing has revolutionised molecular life sciences, however the ISSCR provides guidelines for responsible and ethical research to achieve safe and effective use...
Facilitating productive discussion between scientists, policymakers, and the public surrounding genetic technologies, and their applications, is more crucial than ever...
by Rowda Dahir
The safety and efficiency of CRISPR genome editing can be improved by identifying the best genome editing option for a specific application...
Genome editing is not yet safe for creating germline changes in humans, an international commission has concluded...
CRISPR genome editing may result in unwanted heritable genetic changes, which could lead to long-term risks in a clinical context...
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