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Gene Therapy of Cancer

Overview of attention for book
Cover of 'Gene Therapy of Cancer'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 The Development of Gene Therapy: From Monogenic Recessive Disorders to Complex Diseases Such as Cancer
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    Chapter 2 Designing Adenoviral Vectors for Tumor-Specific Targeting
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    Chapter 3 Analysis of HSV Oncolytic Virotherapy in Organotypic Cultures
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    Chapter 4 Use of Minicircle Plasmids for Gene Therapy
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    Chapter 5 Transposable Elements as Plasmid-Based Vectors for Long-Term Gene Transfer into Tumors
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    Chapter 6 Designing Plasmid Vectors
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    Chapter 7 Development of Bacterial Vectors for Tumor-Targeted Gene Therapy
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    Chapter 8 Electroporative Gene Transfer
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    Chapter 9 Gene Gun Delivery Systems for Cancer Vaccine Approaches
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    Chapter 10 Ultrasound-Mediated Gene Transfection
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    Chapter 11 Nonviral Jet-Injection Technology for Intratumoral In Vivo Gene Transfer of Naked DNA
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    Chapter 12 Methods for Constructing and Evaluating Antitumor DNA Vaccines
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    Chapter 13 Immunity of Lentiviral Vector-Modified Dendritic Cells
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    Chapter 14 Saporin Suicide Gene Therapy
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    Chapter 15 Using In Vivo Biopanning for the Development of Radiation-Guided Drug Delivery Systems
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    Chapter 16 Chemosensitization of Tumor Cells: Inactivation of Nuclear Factor-Kappa B Associated with Chemosensitivity in Melanoma Cells After Combination Treatment with E2F-1 and Doxorubicin
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    Chapter 17 Induction of Tumor Cell Apoptosis by TRAIL Gene Therapy
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    Chapter 18 Silencing Epidermal Growth Factor Receptor by RNA Interference in Glioma
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    Chapter 19 Delivery of phosphorodiamidate morpholino antisense oligomers in cancer cells.
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    Chapter 20 Use of RNA Aptamers for the Modulation of Cancer Cell Signaling
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    Chapter 21 G-Rich Oligonucleotides for Cancer Treatment
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    Chapter 22 Regulatory Aspects for Translating Gene Therapy Research into the Clinic
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    Chapter 23 Ethics of Cancer Gene Transfer Clinical Research
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    Chapter 24 Virus Production for Clinical Gene Therapy
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    Chapter 25 Production of Plasmid DNA as Pharmaceutical
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    Chapter 26 Gene Immunotherapy for Non-Small Cell Lung Cancer
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    Chapter 27 Gene Therapy for Antitumor Vaccination
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    Chapter 28 HSV-tk/IL-2 Gene Therapy for Glioblastoma Multiforme
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    Chapter 29 Construction and Characterization of an Oncolytic HSV Vector Containing a Fusogenic Glycoprotein and Prodrug Activation for Enhanced Local Tumor Control
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    Chapter 30 Newcastle disease virus: a promising vector for viral therapy, immune therapy, and gene therapy of cancer.
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    Chapter 31 Oncolytic Viral Therapy Using Reovirus
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    Chapter 32 Design and Testing of Novel Oncolytic Vaccinia Strains
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    Chapter 33 Tumor-Targeted Salmonella typhimurium Overexpressing Cytosine Deaminase: A Novel, Tumor-Selective Therapy
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    Chapter 34 Chemoprotection by Transfer of Resistance Genes
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    Chapter 35 Phase I Clinical Trial of Locoregional Administration of the Oncolytic Adenovirus ONYX-015 in Combination with Mitomycin-C, Doxorubicin, and Cisplatin Chemotherapy in Patients with Advanced Sarcomas
Attention for Chapter 19: Delivery of phosphorodiamidate morpholino antisense oligomers in cancer cells.
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Chapter title
Delivery of phosphorodiamidate morpholino antisense oligomers in cancer cells.
Chapter number 19
Book title
Gene Therapy of Cancer
Published in
Methods in molecular biology, February 2009
DOI 10.1007/978-1-59745-561-9_19
Pubmed ID
Book ISBNs
978-1-934115-85-5, 978-1-59745-561-9
Authors

Devi, Gayathri R, Devi, Gayathri R., Gayathri R. Devi

Abstract

Phosphorodiamidate morpholino oligomers (PMO), which have a neutral chemistry, are extensively being used as tools for selective inhibition of gene expression in cell culture models and are currently in human clinical trials. PMO oligomers possess a unique structure, in which the deoxyribose moiety of DNA is replaced with a six-membered morpholine ring and the charged phosphodiester internucleoside linkages are replaced with neutral phosphorodiamidate linkages. PMO internalization in uptake-permissive cells has been observed to be specific, saturable, and energy-dependent, suggesting a receptor-mediated uptake mechanism. Understanding PMO transport should facilitate the design of more effective synthetic antisense oligomers as therapeutic agents.

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X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 17%
India 1 17%
Unknown 4 67%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 17%
Professor > Associate Professor 1 17%
Researcher 1 17%
Student > Master 1 17%
Unknown 2 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 50%
Biochemistry, Genetics and Molecular Biology 1 17%
Unknown 2 33%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 02 February 2017.
All research outputs
#18,443,697
of 22,851,489 outputs
Outputs from Methods in molecular biology
#7,922
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Outputs of similar age
#86,781
of 94,282 outputs
Outputs of similar age from Methods in molecular biology
#30
of 38 outputs
Altmetric has tracked 22,851,489 research outputs across all sources so far. This one is in the 11th percentile – i.e., 11% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,127 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 24th percentile – i.e., 24% of its peers scored the same or lower than it.
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