In a world first, researchers from Flinders University have applied advanced gene editing to explore how an enzyme, made ...

An SCD patient in Bahrain received the gene-editing therapy Casgevy, marking the first time the treatment has been given outside the U.S.

Key criticisms of the article include the current inaccuracy of gene-editing technologies, the challenges in accurately identifying causal gene variants, and the possibility of pleiotropic effects ...

Helping these efforts, CHOP haematologist Gerd Blobel, is mapping the transcriptional regulation of fetal haemoglobin. Rather than relying on gene editing or toxic chemotherapies to dial up the ...

highlighting its potential as an efficient and precise tool for gene editing applications. Establishment and robust expansion of human fetal brain organoids, their characterization and adaptation ...

Getty ImagesIn a world first, researchers from Flinders University have applied advanced gene editing to explore how an enzyme, made famous in the ...

Scientists are pushing for reform, arguing that Canada’s law blocks people’s right to benefit from scientific discoveries Ben Schaub “CRISPR” is a powerful gene-editing technology that is ...

With the addition of Casgevy, Children’s Hospital Los Angeles now offers two gene therapies for sickle cell, the first being Lyfgenia.

Gene editing tools like CRISPR/Cas-9 molecular scissors ... Casgevy enables CRISPR/Cas-9 to edit the BCL11A gene in stem cells to produce fetal hemoglobin. The edited genes are infused into ...