TIE: A Method to Electroporate Long DNA Templates into Preimplantation Embryos for CRISPR-Cas9 Gene Editing-Reference-Cited by-同舟云学术

TIE: A Method to Electroporate Long DNA Templates into Preimplantation Embryos for CRISPR-Cas9 Gene Editing

Published:2018-06 Issue:3 Volume:1 Page:223-229
ISSN:2573-1599
Container-title:The CRISPR Journal
language:en
Short-container-title:The CRISPR Journal

Author:

Bagheri Hooman¹²,Friedman Hana¹²³⁴,Shao Harry¹,Chong Yumaine⁵,Lo Chiu-An⁶,Emran Farida⁶,Kays Ibrahim⁶,Yang Xiang-Jiao⁷,Cooper Ellis⁵,Chen Brian E.⁶,Siminovitch Katherine⁸,Peterson Alan¹²³⁴

Affiliation:

1. Laboratory of Developmental Biology, McGill University, Montreal, Quebec, Canada.

2. Department of Human Genetics, McGill University, Montreal, Quebec, Canada.

3. Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.

4. Department of Oncology, McGill University, Montreal, Quebec, Canada.

5. Department of Physiology, McGill University, Montreal, Quebec, Canada.

6. Centre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.

7. Department of Biochemistry, McGill University, Montreal, Quebec, Canada.

8. Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Biotechnology

Link

http://www.liebertpub.com/doi/pdf/10.1089/crispr.2017.0020

Reference29 articles.

1. One-Step Generation of Mice Carrying Reporter and Conditional Alleles by CRISPR/Cas-Mediated Genome Engineering

2. Heritable gene targeting in the mouse and rat using a CRISPR-Cas system

3. Delivery of Cas9 Protein into Mouse Zygotes through a Series of Electroporation Dramatically Increases the Efficiency of Model Creation

4. Generating Mouse Models Using Zygote Electroporation of Nucleases (ZEN) Technology with High Efficiency and Throughput

5. Highly Efficient Mouse Genome Editing by CRISPR Ribonucleoprotein Electroporation of Zygotes

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