gene therapy Although a variety of diseases can be effectively treated, size poses a major problem for some debilitating diseases, such as muscular dystrophy. Genes that...
About 79% of clinical trial participants experienced visible improvement after undergoing CRISPR-based gene editing aimed at curing a rare form of blindness, according to a...
The emergence of RNA viruses like SARS-CoV-2 highlights the need for new methods to combat them. RNA targeting tools like CRISPR/Cas13 are powerful but inefficient in...
Deathcap Mushroom (Amanita) has been a “regicide” for centuries, but may be losing its primacy.Scientists have discovered a possible antidote to a deadly mushroom toxin. Deathcaps,...
CRISPR-Cas9 is widely used to edit genomes by studying genes of interest and altering disease-associated genes. However, this process is accompanied by side effects such as...
CRISPR genome editing is a breakthrough technological breakthrough that earned its founders a Nobel Prize, but this cutting-edge technology is fraught with controversial logistical challenges. At...
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