Stephanie Cherqui and Natalie's Wish: Finding a Gene Therapy for Cystinosis
The story of what has driven UC San Diego's Stephanie Cherqui to develop a gene therapy for Cystinosis, a devastating inherited condition. Series: "Women in Science" [Health and Medicine] [Science] [Show ID: 36222]
Stephanie Cherqui and Natalie's Wish: Finding a Gene Therapy for Cystinosis
The story of what has driven UC San Diego's Stephanie Cherqui to develop a gene therapy for Cystinosis, a devastating inherited condition. Series: "Women in Science" [Health and Medicine] [Science] [Show ID: 36222]
Stephanie Cherqui and Natalie's Wish: Finding a Gene Therapy for Cystinosis
The story of what has driven UC San Diego's Stephanie Cherqui to develop a gene therapy for Cystinosis, a devastating inherited condition. Series: "Women in Science" [Health and Medicine] [Science] [Show ID: 36222]
Stephanie Cherqui and Natalie's Wish: Finding a Gene Therapy for Cystinosis
The story of what has driven UC San Diego's Stephanie Cherqui to develop a gene therapy for Cystinosis, a devastating inherited condition. Series: "Women in Science" [Health and Medicine] [Science] [Show ID: 36222]
Stephanie Cherqui and Natalie's Wish: Finding a Gene Therapy for Cystinosis
The story of what has driven UC San Diego's Stephanie Cherqui to develop a gene therapy for Cystinosis, a devastating inherited condition. Series: "Women in Science" [Health and Medicine] [Science] [Show ID: 36222]
Stephanie Cherqui Discusses Clinical Development of CRISPR Therapies for Rare Diseases
Professor Stephanie Cherqui, UCSD, has worked on the development of cell therapies for two rare genetic diseases, cystinosis and Friedreich’s ataxia. In this interview, Dr. Cherqui chats about her experience working on rare diseases, developing a CRISPR-edited therapy for Friedreich's ataxia, navig…
Prof. Stephanie Cherqui of UCSD on Cystinosis, Friedreich’s ataxia, Alzheimer’s and gene therapy
Scientific Sense ® by Gill Eapen: Prof. Stephanie Cherqui is professor of Pediatrics at the University of California San Diego. Her research project is focused on the molecular characterization of cystinosis, a metabolic hereditary disease, and gene therapy.
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Hematopoietic Stem Cell Gene Therapy for Cystinosis
In this episode I'm joined by senior author Dr. Stephanie Cherqui to talk about her recent publication in the New England Journal of Medicine on gene therapy for cystinosis. This is a very personal episode for me, because two of my children have cystinosis. The article is linked below. Thanks for l…
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