Two complementary studies led by researchers from the Yong Loo Lin School of Medicine, National University of Singapore (NUS ...
医学Medicine2025年10月23日,由复旦大学领衔的全球首个遗传性耳聋基因治疗国际专家共识在Cell Press细胞出版社旗下医学旗舰刊Med上正式发布[1],并登上Cell Press官网头条。论文题为“International ...
细胞与基因疗法 (Cell and Gene Therapy,CGT)正以前所未有的速度重塑现代医学的边界。自2017年首款 CART 疗法获批以来,CGT ...
Fred Hutch bioengineer Dr. Matthias Stephan is working to develop a special foam that could help make gene therapy for blood ...
Scientists at St. Jude Children's Research Hospital and Northwestern University identified a previously unknown treatment ...
At the end of last year, the field of cell and gene therapy was on a high following the landmark approval of the first genome-editing therapy, Casgevy (exagamglogene autotemcel), which was developed ...
Chronic diseases once meant a lifetime of management. But a new generation of cell and gene therapies is challenging that paradigm. Markets are responding. The global cell and gene therapy market is ...
Miguel Forte, current President of the International Society for Cell & Gene Therapy (ISCT), joins Blue Cell as a Non-Executive Director -- Highly experienced executive with deep scientific expertise, ...
New state-of-the-art facility in Philadelphia provides integrated lab and collaboration space along with tailored guidance to help move advanced therapies from early research to clinical readiness ...
The Times of Israel on MSN
In world first, Israeli scientists use RNA-based gene therapy to stop ALS deterioration
By adding a microRNA molecule to ALS models, Tel Aviv University, Ben-Gurion University and Weizmann Institute researchers ...
UCSF Benioff Children’s Hospital Oakland is enrolling patients in an innovative clinical trial that seeks to cure sickle cell disease. The trial is the first in the U.S. to apply non-viral CRISPR-Cas9 ...
MeiraGTx is cashing in on a gene therapy that restored vision to 11 children who were born legally blind, licensing the ...
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