CRISPR/Cas9 technology as a potent molecular tool for gene therapy-Reference-Cited by-同舟云学术

CRISPR/Cas9 technology as a potent molecular tool for gene therapy

Published:2019-01-30 Issue:8 Volume:234 Page:12267-12277
ISSN:0021-9541
Container-title:Journal of Cellular Physiology
language:en
Short-container-title:J Cell Physiol

Author:

Karimian Ansar¹²³,Azizian Khalil⁴,Parsian Hadi¹,Rafieian Sona⁵,Shafiei‐Irannejad Vahid⁶,Kheyrollah Maryam⁷,Yousefi Mehdi⁸⁹^ORCID,Majidinia Maryam¹⁰^ORCID,Yousefi Bahman¹¹¹²

Affiliation:

1. Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences Babol Iran

2. Cancer & Immunology Research Center, Kurdistan University of Medical Sciences Sanandaj Iran

3. Student Research Committee, Babol University of Medical Sciences Babol Iran

4. Liver and Gastrointestinal Diseases Research Center, Tabriz University of Medical Science Tabriz Iran

5. Department of Oral and Maxillofacial Pathology School of Dentistry, Zanjan University of Medical Sciences Zanjan Iran

6. Cellular and Molecular Research Center, Urmia University of Medical Sciences Urmia Iran

7. Department of Molecular Medicine National Institue of Genetic Engeneering and Biotechnology Tehran Iran

8. Molecular Medicine Research Center, Tabriz University of Medical Sciences Tabriz Iran

9. Immunology Research Center, Tabriz University of Medical Sciences Tabriz Iran

10. Tumor Research Center, Urmia University of Medical Sciences Urmia Iran

11. Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences Tehran Iran

12. Department of Biochemistry and Clinical Laboratories Faculty of Medicine, Tabriz University of Medical Science Tabriz Iran

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcp.27972

Reference87 articles.

1. Clustered regularly interspaced short palindromic repeats (CRISPRs): the hallmark of an ingenious antiviral defense mechanism in prokaryotes

2. CRISPR–Cas adaptation: insights into the mechanism of action

3. Suppression of p53R2 gene expression with specific siRNA sensitizes HepG2 cells to doxorubicin

4. CRISPR Provides Acquired Resistance Against Viruses in Prokaryotes

5. Structure and activity of the Cas3 HD nuclease MJ0384, an effector enzyme of the CRISPR interference

Cited by 98 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives;Computational and Structural Biotechnology Journal;2024-12

2. Gene therapy for polygenic or complex diseases;Biomarker Research;2024-09-04

3. Role of CRISPR‐Cas systems in periodontal disease pathogenesis and potential for periodontal therapy: A review;Molecular Oral Microbiology;2024-09-03

4. CRISPR-CAS9-MEDIATED EX VIVO GENE EDITING FOR INHERITED HEMATOLOGICAL DISORDERS: ADVANCEMENTS, CHALLENGES, AND CLINICAL POTENTIAL;International Journal of Pharmacy and Pharmaceutical Sciences;2024-09-01

5. A review on molecular scissoring with CRISPR/Cas9 genome editing technology;Toxicology Research;2024-07-01