Topic
Gene Editing and CRISPR
Scientists have developed groundbreaking tools to alter the expression of the human genome, and the mastery of these tools is on the horizon.
Gene editing is already providing new therapies for rare diseases that just a generation ago were untreatable. New techniques with CRISPR hold promise for greatly improving both quality and length of life for those suffering from genetic conditions.
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Scientist Wins Prestigious Bowes Biomedical Investigator Award for Finding ‘Anti-CRISPRs’
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Human Proteins Behind COVID-19 Infection Revealed by Innovative CRISPR Technology
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Sickle Cell Clinical Trial Aims to Cure Disease by Correcting Patient’s Mutated Gene
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Infecting Gut Microbes with CRISPR-loaded Virus Demonstrates Potential for Microbiome Gene Editing
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Scientists Map Brain Circuit that Drives Activity in Fertile Females
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Gene Therapy Offers Long-Awaited Hope for Children with Rare, Incurable Disorder
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Next-Generation T-Cell Therapeutics Set Sights on Cancers, Autoimmune Disorders and More
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Living Therapeutics Initiative Will Accelerate Development and Delivery of Revolutionary Treatments