• Home
  • Browse
    • Current Issue
    • By Issue
    • By Author
    • By Subject
    • Author Index
    • Keyword Index
  • Journal Info
    • About Journal
    • Aims and Scope
    • Editorial Board
    • Publication Ethics
    • Peer Review Process
  • Guide for Authors
  • Submit Manuscript
  • Contact Us
 
  • Login
  • Register
Home Articles List Article Information
  • Save Records
  • |
  • Printable Version
  • |
  • Recommend
  • |
  • How to cite Export to
    RIS EndNote BibTeX APA MLA Harvard Vancouver
  • |
  • Share Share
    CiteULike Mendeley Facebook Google LinkedIn Twitter
Suez Canal University Medical Journal
arrow Articles in Press
arrow Current Issue
Journal Archive
Volume Volume 28 (2025)
Volume Volume 27 (2024)
Volume Volume 26 (2023)
Volume Volume 25 (2022)
Volume Volume 24 (2021)
Volume Volume 23 (2020)
Volume Volume 22 (2019)
Volume Volume 21 (2018)
Volume Volume 20 (2017)
Issue Issue 2
Issue Issue 1
Volume Volume 19 (2016)
Volume Volume 18 (2015)
Volume Volume 17 (2014)
Volume Volume 16 (2013)
Volume Volume 15 (2012)
Volume Volume 14 (2011)
Volume Volume 13 (2010)
Hassan, R. (2017). Genome Editing and Chimeric Antigen Receptors T Cell Therapy. Suez Canal University Medical Journal, 20(2), 122-127. doi: 10.21608/scumj.2017.43560
Ranya Hassan. "Genome Editing and Chimeric Antigen Receptors T Cell Therapy". Suez Canal University Medical Journal, 20, 2, 2017, 122-127. doi: 10.21608/scumj.2017.43560
Hassan, R. (2017). 'Genome Editing and Chimeric Antigen Receptors T Cell Therapy', Suez Canal University Medical Journal, 20(2), pp. 122-127. doi: 10.21608/scumj.2017.43560
Hassan, R. Genome Editing and Chimeric Antigen Receptors T Cell Therapy. Suez Canal University Medical Journal, 2017; 20(2): 122-127. doi: 10.21608/scumj.2017.43560

Genome Editing and Chimeric Antigen Receptors T Cell Therapy

Editorial, Volume 20, Issue 2, October 2017, Page 122-127  XML PDF (819.83 K)
DOI: 10.21608/scumj.2017.43560
View on SCiNiTO View on SCiNiTO
Author
Ranya Hassan email
Clinical pathology Department, Faculty of Medicine, Suez Canal university, Egypt
Abstract
Recent advances in genome editing technologies have significantly enhanced making specific changes in the genomes of different types cells. Genetically engineered T cells, or the 'living drugs', is considered a new era in antitumor therapy. Current clinical trials using chimeric antigen receptors (CARs) T cells showed a promising result in patients with some intractable hematological malignancies. In this Review, some of the most recent advances in CAR T cell therapy are mentioned high lightening the use of genome editing in this field.
Keywords
CRISPR/Cas9; chimeric antigen receptor; T lymphocytes; gene therapy
Statistics
Article View: 217
PDF Download: 444
Home | Glossary | News | Aims and Scope | Sitemap
Top Top

Journal Management System. Designed by NotionWave.