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Volumn 20, Issue 5, 2013, Pages 575-580
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Inhibition of TGF-β signaling in genetically engineered tumor antigen-reactive T cells significantly enhances tumor treatment efficacy
a a b a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
RETROVIRUS VECTOR;
SMAD2 PROTEIN;
TRANSFORMING GROWTH FACTOR BETA2;
TUMOR ANTIGEN;
TYROSINASE RELATED PROTEIN 1;
ANIMAL CELL;
ARTICLE;
CANCER IMMUNOTHERAPY;
CD4+ T LYMPHOCYTE;
CD8+ T LYMPHOCYTE;
CELL ENGINEERING;
CELL TRANSFER;
ENZYME INHIBITION;
IN VITRO STUDY;
IN VIVO STUDY;
MELANOMA B16;
MOUSE;
NONHUMAN;
PRIORITY JOURNAL;
PROTEIN EXPRESSION;
PROTEIN PHOSPHORYLATION;
SIGNAL TRANSDUCTION;
T LYMPHOCYTE;
WESTERN BLOTTING;
ANIMALS;
ANTIGEN-PRESENTING CELLS;
APOPTOSIS;
CD8-POSITIVE T-LYMPHOCYTES;
CELL LINE, TUMOR;
GENETIC ENGINEERING;
GENETIC VECTORS;
HUMANS;
IMMUNOGLOBULIN FC FRAGMENTS;
IMMUNOGLOBULIN G;
IMMUNOTHERAPY;
MELANOMA, EXPERIMENTAL;
MICE;
PROTEIN-SERINE-THREONINE KINASES;
RECEPTORS, TRANSFORMING GROWTH FACTOR BETA;
RECOMBINANT FUSION PROTEINS;
RETROVIRIDAE;
SIGNAL TRANSDUCTION;
T-LYMPHOCYTES;
TRANSFORMING GROWTH FACTOR BETA;
TREATMENT OUTCOME;
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EID: 84877788719
PISSN: 09697128
EISSN: 14765462
Source Type: Journal
DOI: 10.1038/gt.2012.75 Document Type: Article |
Times cited : (83)
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References (0)
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