scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1041142465 |
P356 | DOI | 10.1038/GT.2014.67 |
P698 | PubMed publication ID | 25077772 |
P50 | author | Meng-Chi Yen | Q60679346 |
P2093 | author name string | C-Y Wang | |
J-Y Chang | |||
Y-L Chen | |||
M-D Lai | |||
C-T Huang | |||
W-C Chen | |||
J-J Hung | |||
T-Y Weng | |||
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Progression to Malignancy in the Polyoma Middle T Oncoprotein Mouse Breast Cancer Model Provides a Reliable Model for Human Diseases | Q34272277 | ||
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Xenogeneic Human p53 DNA Vaccination by Electroporation Breaks Immune Tolerance to Control Murine Tumors Expressing Mouse p53 | Q34607207 | ||
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Direct T cell activation via CD40 ligand generates high avidity CD8+ T cells capable of breaking immunological tolerance for the control of tumors | Q37659577 | ||
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Skin delivery of short hairpin RNA of indoleamine 2,3 dioxygenase induces antitumor immunity against orthotopic and metastatic liver cancer. | Q39478032 | ||
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Different types of K-Ras mutations could affect drug sensitivity and tumour behaviour in non-small-cell lung cancer | Q44425380 | ||
CD8+ T cells, NK cells and IFN-gamma are important for control of tumor with downregulated MHC class I expression by DNA vaccination | Q45864088 | ||
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P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 888-896 | |
P577 | publication date | 2014-07-31 | |
P1433 | published in | Gene Therapy | Q15763095 |
P1476 | title | DNA vaccine elicits an efficient antitumor response by targeting the mutant Kras in a transgenic mouse lung cancer model | |
P478 | volume | 21 |
Q92783310 | ADAM17: An Emerging Therapeutic Target for Lung Cancer |
Q55079595 | Homoharringtonine induced immune alteration for an Efficient Anti-tumor Response in Mouse Models of Non-small Cell Lung Adenocarcinoma Expressing Kras Mutation. |
Q99237818 | Recombinant KRAS G12D Protein Vaccines Elicit Significant Anti-Tumor Effects in Mouse CT26 Tumor Models |
Q47137503 | Skin Delivery of Clec4a Small Hairpin RNA Elicited an Effective Antitumor Response by Enhancing CD8+ Immunity In Vivo. |
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