scholarly journals Dual target gene therapy to EML4-ALK NSCLC by a gold nanoshell-based system: Erratum

Theranostics ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 2402-2404
Author(s):  
Siwen Li ◽  
Yuxi Liu ◽  
Yalan Rui ◽  
Liping Tang ◽  
Samuel Achilefu ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Target Gene ◽  
Gold Nanoshell ◽  
Target Gene Therapy ◽  
Dual Target

scholarly journals Dual target gene therapy to EML4-ALK NSCLC by a gold nanoshell-based system

Theranostics ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 2621-2633 ◽  
Author(s):  
Siwen Li ◽  
Yuxi Liu ◽  
Yalan Rui ◽  
Liping Tang ◽  
Samuel Achilefu ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Target Gene ◽  
Gold Nanoshell ◽  
Target Gene Therapy ◽  
Dual Target

Target gene therapy for alpha-fetoprotein producing hepatocellular carcinoma by E1B55k-attenuated adenovirus

2001 ◽  
Vol 120 (5) ◽  
pp. A361-A361
Author(s):  
M OHASHI ◽  
F KANAI ◽  
K TATEISHI ◽  
H TANIGUCHI ◽  
H HAMADA ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Gene Therapy ◽  
Target Gene ◽  
Alpha Fetoprotein ◽  
Target Gene Therapy

PC38 USE OF MACROPHAGES TO TARGET GENE THERAPY TO HYPOXIC AREAS OF PROSTATE TUMOURS

2004 ◽  
Vol 11 (6) ◽  
pp. 551-552
Author(s):  
E. J. MacRae ◽  
N. J. Brown ◽  
C. E. Lewis
Keyword(s):  
Gene Therapy ◽  
Target Gene ◽  
Target Gene Therapy

Target Gene Therapy for α-Fetoprotein-Producing Hepatocellular Carcinoma by E1B55k-Attenuated Adenovirus

2001 ◽  
Vol 282 (2) ◽  
pp. 529-535 ◽  
Author(s):  
Makoto Ohashi ◽  
Fumihiko Kanai ◽  
Keisuke Tateishi ◽  
Hiroyoshi Taniguchi ◽  
Paola A. Marignani ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Gene Therapy ◽  
Target Gene ◽  
Target Gene Therapy

scholarly journals Target gene therapy of glioma: overexpression of BAX gene under the control of both tissue-specific promoter and hypoxia-inducible element

2010 ◽  
Vol 42 (4) ◽  
pp. 274-280 ◽  
Author(s):  
J. Huang ◽  
J. Gao ◽  
X. Lv ◽  
G. Li ◽  
D. Hao ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Target Gene ◽  
Tissue Specific ◽  
Tissue Specific Promoter ◽  
Target Gene Therapy ◽  
Bax Gene

scholarly journals A Moving Target Gene Therapy: Therapeutic Mechanisms and Strategies

2001 ◽  
Vol 3 (4) ◽  
pp. 429-430
Author(s):  
Fintan R. Steele
Keyword(s):  
Gene Therapy ◽  
Target Gene ◽  
Moving Target ◽  
Therapeutic Mechanisms ◽  
Target Gene Therapy

Target gene therapy for alpha-fetoprotein producing hepatocellular carcinoma by E1B55k-attenuated adenovirus

2001 ◽  
Vol 120 (5) ◽  
pp. A361
Author(s):  
Makoto Ohashi ◽  
Fumihiko Kanai ◽  
Keisuke Tateishi ◽  
Hiroyoshi Taniguchi ◽  
Hirofumi Hamada ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Gene Therapy ◽  
Target Gene ◽  
Alpha Fetoprotein ◽  
Target Gene Therapy

scholarly journals Photothermal and gene therapy combined with immunotherapy to gastric cancer by the gold nanoshell-based system

2019 ◽  
Vol 17 (1) ◽  
Author(s):  
Jiayu Zhang ◽  
Tiancheng Zhao ◽  
Fanglei Han ◽  
Yu Hu ◽  
Yezhou Li
Keyword(s):  
Gastric Cancer ◽  
Gene Therapy ◽  
Gold Nanoshell

scholarly journals TREATMENT POSSIBILITIES FOR ACQUIRED AND HEREDITARY DISEASES BY GENE THERAPY: A REVIEW

2021 ◽  
pp. 26-32
Author(s):  
P. V. KAMALA KUMARI ◽  
G. EKSHITHA, V. HARIKA
Keyword(s):  
Gene Therapy ◽  
Nucleic Acids ◽  
Viral Vectors ◽  
Target Gene ◽  
Genetic Diseases ◽  
Hereditary Diseases ◽  
Root Cause ◽  
Delivery Strategies ◽  
Foreign Genes ◽  
And Control

Therapeutic nucleic acids demand specificity and accuracy in design as well as delivery strategies used in replacement or silencing of the target gene. Gene therapy is believed to be the therapy in which the root cause of the diseases can be treated at the molecular level. Generally gene therapy helps in the identification of the origin of the disorder instead of using drugs to diminish or control the symptoms. The application of nucleic acids to treat and control diseases is known as “gene therapy.” Gene therapy consists on the substitution or addition of a functional gene into the nucleus of a living cell, in order to treat a disease or repair a dysfunction, caused by this gene failure. This therapy is used to correct defective genes, which are responsible for genetic diseases. Thus, gene therapy can be used to prevent, treat or regulate hereditary or acquired disorders, by the production of therapeutic proteins. The gene therapy is mediated by the use of viral and non-viral vectors to transport foreign genes into somatic cells to restorative defective genes. This review focuses on viral vectors in detail.

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