(Q37003699)

English

Immunoresistant human glioma cell clones selected with alloreactive cytotoxic T lymphocytes: downregulation of multiple proapoptotic factors

scientific article published on June 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Immunoresistant human glioma cell clones selected with alloreactive cytotoxic T lymphocytes: downregulation of multiple proapoptotic factors (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

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author name string

German G Gomez

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Michelle J Hickey

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Richard Tritz

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Carol A Kruse

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

publication date

1 June 2008

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Gene therapy & molecular biology

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

12

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

101-110

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Cellular and functional characterization of immunoresistant human glioma cell clones selected with alloreactive cytotoxic T lymphocytes reveals their up-regulated synthesis of biologically active TGF-beta

1 reference

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Mechanisms of malignant glioma immune resistance and sources of immunosuppression

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Genomic alterations in human malignant glioma cells associate with the cell resistance to the combination treatment with tumor necrosis factor-related apoptosis-inducing ligand and chemotherapy

1 reference

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Isolation of immunoresistant human glioma cell clones after selection with alloreactive cytotoxic T lymphocytes: cytogenetic and molecular cytogenetic characterization

1 reference

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Dendritic cell vaccination in glioblastoma patients induces systemic and intracranial T-cell responses modulated by the local central nervous system tumor microenvironment

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Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma

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ATM, a central controller of cellular responses to DNA damage.

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DFF45/ICAD can be directly processed by granzyme B during the induction of apoptosis

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T cell adoptive immunotherapy of newly diagnosed gliomas

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Initiation of Apaf-1 translation by internal ribosome entry

1 reference

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Apaf1 is required for mitochondrial pathways of apoptosis and brain development

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Apaf-1, a human protein homologous to C. elegans CED-4, participates in cytochrome c-dependent activation of caspase-3

1 reference

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Eradication of established intracranial rat gliomas by transforming growth factor beta antisense gene therapy

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Analysis of interleukin 2 and various effector cell populations in adoptive immunotherapy of 9L rat gliosarcoma: allogeneic cytotoxic T lymphocytes prevent tumor take

1 reference

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Treatment of recurrent glioma with intracavitary alloreactive cytotoxic T lymphocytes and interleukin-2.

1 reference

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Role of Fas ligand (CD95L) in immune escape: the tumor cell strikes back

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Allogeneic tumor-specific cytotoxic T lymphocytes

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A 9L gliosarcoma transplantation model for studying adoptive immunotherapy into the brains of conscious rats

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Inhibition of DNA methylation sensitizes glioblastoma for tumor necrosis factor-related apoptosis-inducing ligand-mediated destruction

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Frequent LOH at chromosome 12q22-23 and Apaf-1 inactivation in glioblastoma

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Human Alloreactive CTL Interactions with Gliomas and with Those Having Upregulated HLA Expression from Exogenous IFN-γ or IFN-γ Gene Modification

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ATM protein expression correlates with radioresistance in primary glioblastoma cells in culture.

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Artificial-capillary-system development of human alloreactive cytotoxic T-lymphocytes that lyse brain tumours.

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Intracranial administrations of single or multiple source allogeneic cytotoxic T lymphocytes: chronic therapy for primary brain tumors

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4 December 2018

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

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