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Related Concept Videos

CRISPR and crRNAs02:53

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Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
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CRISPR/Cas9 Genome Editing01:28

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The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
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CRISPR01:59

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Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
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Updated: Oct 17, 2025

Production, Purification, and Quality Control for Adeno-associated Virus-based Vectors
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CRISPR Systems Suitable for Single AAV Vector Delivery.

Marta Stevanovic1, Elena Piotter1, Michelle E McClements1

  • 1Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences and NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, United Kingdom.

Current Gene Therapy
|October 8, 2021
PubMed
Summary
This summary is machine-generated.

Smaller CRISPR/Cas gene editing proteins are crucial for efficient delivery via adeno-associated viral (AAV) vectors. This review explores small Cas orthologs for improved in vivo gene editing therapies.

Failed At:

2026-06-19T13:39:10.566643+00:00

Keywords:
AAVCRISPRCRISPR/Cas9Cas9gene therapyorthologs

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