Protocol for establishing knockout cell clones by deletion of a large gene fragment using CRISPR-Cas9 with multiple guide RNAs-Reference-Cited by-同舟云学术

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Protocol for establishing knockout cell clones by deletion of a large gene fragment using CRISPR-Cas9 with multiple guide RNAs

Published:2024-09 Issue:3 Volume:5 Page:103179
ISSN:2666-1667
Container-title:STAR Protocols
language:en
Short-container-title:STAR Protocols

Author:

Saito Akira C.,Higashi Tomohito^ORCID,Chiba Hideki

Publisher

Elsevier BV

Reference17 articles.

1. Occludin and tricellulin facilitate formation of anastomosing tight-junction strand network to improve barrier function;Saito;MBoC,2021

2. Effects of TAMP family on the tight junction strand network and barrier function in epithelial cells;Saito;Ann. N. Y. Acad. Sci.,2022

3. EpCAM proteolysis and release of complexed claudin-7 repair and maintain the tight junction barrier;Higashi;J. Cell Biol.,2023

4. Clostridium perfringens enterotoxin fragment removes specific claudins from tight junction strands: Evidence for direct involvement of claudins in tight junction barrier;Sonoda;J. Cell Biol.,1999

5. Predicting base editing outcomes with an attention-based deep learning algorithm trained on high-throughput target library screens;Marquart;Nat. Commun.,2021

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