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Related Concept Videos

CRISPR01:59

CRISPR

49.8K
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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Homologous Recombination02:31

Homologous Recombination

50.3K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
50.3K
CRISPR and crRNAs02:53

CRISPR and crRNAs

16.9K
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...
16.9K

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Genome scale CRISPRi reveals both shared and strain-specific vulnerabilities in genetically diverse drug-resistant strains of Mycobacterium tuberculosis.

Nature communications·2026
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Mismatch type impacts interference and priming activities in the type I-E CRISPR-Cas system.

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Mismatch type impacts interference and priming activities in the type I-E CRISPR-Cas system.

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Viral surveillance of invasive mammals in New Zealand reveals unique viral lineages reflecting their introduction history.

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Towards a phylogenetically informed approach to solving protein-protein interactions.

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Regulation of anti-CRISPR operons by structurally distinct families of Aca proteins.

Communications biology·2025

Related Experiment Video

Updated: Jun 13, 2025

Genome Editing in Mammalian Cell Lines using CRISPR-Cas
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Genome Editing in Mammalian Cell Lines using CRISPR-Cas

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CRISPR2025 New Zealand: Innovation and Collaboration

Katharina G Wandera1, Jeremy Dubrulle1, Russell Greene2

  • 1Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.

The CRISPR Journal
|May 28, 2025
PubMed
Summary

No abstract available in PubMed .

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