(Q43703250)

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Efficacy of the bystander effect in the herpes simplex virus thymidine kinase-mediated gene therapy is influenced by the expression of connexin43 in the target cells

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Europe PubMed Central

PubMed publication ID

26 November 2017

Efficacy of the bystander effect in the herpes simplex virus thymidine kinase-mediated gene therapy is influenced by the expression of connexin43 in the target cells (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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author name string

Namba H

1

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Iwadate Y

2

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Kawamura K

3

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Sakiyama S

4

1 reference

Europe PubMed Central

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26 November 2017

Tagawa M

5

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

publication date

1 June 2001

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Europe PubMed Central

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26 November 2017

Cancer Gene Therapy

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Europe PubMed Central

PubMed publication ID

26 November 2017

8

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Europe PubMed Central

PubMed publication ID

26 November 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

414-420

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Europe PubMed Central

PubMed publication ID

26 November 2017

Regression of established macroscopic liver metastases after in situ transduction of a suicide gene

1 reference

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Development of anti-tumor immunity following thymidine kinase-mediated killing of experimental brain tumors

1 reference

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The effect of thymidine kinase transduction and ganciclovir therapy on tumor vasculature and growth of 9L gliomas in rats

1 reference

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Transfection of C6 glioma cells with connexin 43 cDNA: analysis of expression, intercellular coupling, and cell proliferation

1 reference

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7 January 2021

based on heuristic

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The extent of heterocellular communication mediated by gap junctions is predictive of bystander tumor cytotoxicity in vitro

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

The bystander effect exerted by tumor cells expressing the herpes simplex virus thymidine kinase (HSVtk) gene is dependent on connexin expression and cell communication via gap junctions

1 reference

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Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins

1 reference

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based on heuristic

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Protein and messenger RNA expression of connexin43 in astrocytomas: implications in brain tumor gene therapy

1 reference

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The TMC Worldwide Gene Therapy Enrollment Report, end 1996.

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Targeted killing of migrating glioma cells by injection of HTK-modified glioma cells

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Bystander effect-mediated therapy of experimental brain tumor by genetically engineered tumor cells

1 reference

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based on heuristic

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Treatment of rat experimental brain tumors by herpes simplex virus thymidine kinase gene-transduced allogeneic tumor cells and ganciclovir

1 reference

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Interleukin-2 gene-transduced human melanoma cells efficiently stimulate MHC-unrestricted and MHC-restricted autologous lymphocytes

1 reference

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Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

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Evaluation of the bystander effect in experimental brain tumors bearing herpes simplex virus-thymidine kinase gene by serial magnetic resonance imaging

1 reference

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Bystander tumoricidal effect in the treatment of experimental brain tumors

1 reference

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based on heuristic

inferred from DOI database lookup

Connexins are expressed in primary brain tumors and enhance the bystander effect in gene therapy

1 reference

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based on heuristic

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Retinoids augment the bystander effect in vitro and in vivo in herpes simplex virus thymidine kinase/ganciclovir-mediated gene therapy

1 reference

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Gene therapy of experimental brain tumors using neural progenitor cells

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Identifiers

10.1038/SJ.CGT.7700317

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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https://api.fatcat.wiki/v0/release/kzgijcl5rnfb5hpxhuidjqir5a

24 November 2022

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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