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Modeling Disease In Vivo With CRISPR/Cas9
1Department of Medicine, Hematology and Medical Oncology, Weill Cornell Medical College, New York, NY 10021, USA.
Trends in Molecular Medicine
|October 4, 2015
Summary
CRISPR/Cas9 genome editing offers a powerful new method for genetic manipulation. This technology is advancing the creation of in vivo disease models, particularly for studying complex human cancers.
Area of Science:
- Genetics and Genomics
- Molecular Biology
- Biotechnology
Background:
- CRISPR/Cas9 genome editing technology has emerged as a revolutionary tool in biological research.
- Its simplicity and effectiveness enable precise genomic manipulation across diverse cell types.
- The technology is derived from an adaptive bacterial immune system.
Purpose of the Study:
- To discuss the current applications of CRISPR technology.
- To highlight the development of novel in vivo disease models using CRISPR.
- To emphasize the utility of CRISPR in modeling human cancer complexity.
Main Methods:
- CRISPR/Cas9-mediated genome editing.
- Development of in vivo models.
- Application in cancer research.
Main Results:
- CRISPR/Cas9 has become a preferred tool for genetic manipulation.
- The technology facilitates the creation of new in vivo disease models.
- CRISPR-derived tools enhance the modeling of human cancer.
Conclusions:
- CRISPR/Cas9 technology provides a promising platform for studying gene function in vivo.
- Its application in creating disease models, especially for cancer, is rapidly advancing.
- This technology holds significant potential for future biomedical research and therapeutic development.
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