(Q33956820)

30 July 2017

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title

Gene therapy for cancer: from the laboratory to the patient (English)

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30 July 2017

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Kouraklis G

1

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PubMed ID

10877214

30 July 2017

language of work or name

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1 June 2000

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Digestive Diseases and Sciences

30 July 2017

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30 July 2017

45

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30 July 2017

1045-1052

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30 July 2017

6

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https://scigraph.springernature.com/pub.10.1023/a:1005592309466

30 July 2017

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cites work

Progress toward human gene therapy

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12 December 2020

Interleukin-2 gene therapy in a patient with glioblastoma

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12 December 2020

Gene therapy for cancer

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Dysfunction of the E-cadherin/catenin cell adhesion cascade in epithelial cancers (Review).

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A gene transfer strategy for making bone marrow cells resistant to trimetrexate

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Immunization of cancer patients using autologous cancer cells modified by insertion of the gene for interleukin-2

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Progress in cancer gene therapy

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Induction of antitumor immunity by recombinant vaccinia viruses expressing B7-1 or B7-2 costimulatory molecules.

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Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy.

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Second-generation adenovirus vectors

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In Vivo Gene Transfer with Retroviral Vector-Producer Cells for Treatment of Experimental Brain Tumors

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Immunotherapy of malignancy by in vivo gene transfer into tumors

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Retrovirus-mediated expression of a DNA repair protein in bone marrow protects hematopoietic cells from nitrosourea-induced toxicity in vitro and in vivo.

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Cancer gene therapy annual conference 1997: trends and news

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Newer immunologic approaches to the treatment of patients with melanoma

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Selection of drug-resistant bone marrow cells in vivo after retroviral transfer of human MDR1

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Modification of tumor suppressor gene expression in non-small cell lung cancer (NSCLC) with a retroviral vector expressing wildtype (normal) p53

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Human gene therapy comes of age.

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Molecular biology and therapy of disease

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The roles of herpes simplex virus in neuroscience.

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A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase

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Stable expression of selectable genes introduced into human hematopoietic stem cells by electric field-mediated DNA transfer

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Retroviral transduction of CD34-enriched hematopoietic progenitor cells under serum-free conditions

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The N2-TIL human gene transfer clinical protocol

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Tissue-specific targeting of retroviral vectors through ligand-receptor interactions

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Nondefective spleen necrosis virus-derived vectors define the upper size limit for packaging reticuloendotheliosis viruses

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Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis

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Retroviral vector-mediated transduction of K-ras antisense RNA into human lung cancer cells inhibits expression of the malignant phenotype

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The ADA human gene therapy clinical protocol

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Construction and expression in tumor cells of a recombinant vaccinia virus encoding human interleukin-1 beta

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Systemic gene expression after intravenous DNA delivery into adult mice

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Adenovirally transferred p16INK4/CDKN2 and p53 genes cooperate to induce apoptotic tumor cell death

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Gene expression in mice after high efficiency retroviral-mediated gene transfer

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Cancer gene therapy: principles, problems, and perspectives.

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12 December 2020

Herpes simplex virus vectors for gene therapy

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Induction of chemosensitivity in human lung cancer cells in vivo by adenovirus-mediated transfer of the wild-type p53 gene

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High-efficiency gene transfer mediated by adenovirus coupled to DNA-polylysine complexes

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Prolonged transgene expression in cotton rat lung with recombinant adenoviruses defective in E2a.

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Cell cycle arrest and inhibition of tumor cell proliferation by the p16INK4 gene mediated by an adenovirus vector

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In vivo promoter activity and transgene expression in mammalian somatic tissues evaluated by using particle bombardment

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A third-generation lentivirus vector with a conditional packaging system

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12 December 2020

A defective herpes simplex virus vector system for gene delivery into the brain: comparison with alternative gene delivery systems and usefulness for gene therapy.

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Hepatic gene therapy: efficient gene delivery and expression in primary hepatocytes utilizing a conjugated adenovirus-DNA complex

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Enhanced tumor suppressor gene therapy via replication-deficient adenovirus vectors expressing an N-terminal truncated retinoblastoma protein

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A brief history of gene therapy

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12 December 2020

Binding of transcription factors and creation of a large nucleoprotein complex on the human cytomegalovirus enhancer

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Targeted delivery of antisense oligonucleotides by molecular conjugates

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A packaging cell line for propagation of recombinant adenovirus vectors containing two lethal gene-region deletions

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Transfer of genes to humans: early lessons and obstacles to success

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Interleukin-2: inception, impact, and implications

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12 December 2020

The development of new cancer therapies based on the molecular identification of cancer regression antigens

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12 December 2020

Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver

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12 December 2020

Cancer gene therapy: connecting basic research with clinical inquiry

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12 December 2020

Gene therapy for cancer

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12 December 2020

Progress in the development of an HIV-1 vaccine

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12 December 2020

Gene therapy of cancer through restoration of tumor-suppressor functions?

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12 December 2020

Use of tissue-specific expression of the herpes simplex virus thymidine kinase gene to inhibit growth of established murine melanomas following direct intratumoral injection of DNA.

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12 December 2020

Gene therapy using adenoviral vectors

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12 December 2020

Expression of a tumor-reactive antibody-interleukin 2 fusion protein after in vivo particle-mediated gene delivery

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12 December 2020

Identifiers

DOI

10.1023/A:1005592309466

1 reference

PubMed ID

10877214

Dimensions Publication ID

30 July 2017

0 references

1 reference

PubMed ID

10877214