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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New CRISPR Center Brings Hope for Rare and Deadly Genetic Diseases
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UCSF Health Experts Spotlight Advances at Hematology Conference
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Pioneering Sickle Cell Care and Research for 50 Years
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Gene Editing of Microbiome May Help Prevent Asthma in Children
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How Gene Therapy Saved a Child from ‘Bubble Boy’ Disease
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The Surgeon Set on Curing Genetic Diseases Before Birth
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Editing Genes in the Microbiome to Prevent Disease
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Thermo Fisher Scientific Opens Cell Therapy Facility at UCSF to Accelerate Development of Breakthrough Therapies