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Sequential loss of cytotoxic T lymphocyte responses to simian virus 40 large T antigen epitopes in t antigen transgenic mice developing osteosarcomas
Todd D. Schell
, Barbara B. Knowles
, Satvir S. Tevethia
Penn State Cancer Institute
Cancer Institute, Mechanisms of Carcinogenesis
Department of Cell and Biological Systems
Research output
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Contribution to journal
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Article
›
peer-review
47
Scopus citations
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Dive into the research topics of 'Sequential loss of cytotoxic T lymphocyte responses to simian virus 40 large T antigen epitopes in t antigen transgenic mice developing osteosarcomas'. Together they form a unique fingerprint.
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Keyphrases
Transgenic Mice
100%
Epitope
100%
Antigenic Epitope
100%
Osteosarcoma
100%
Cytotoxic T Cell Response
100%
Simian Virus 40 Large T Antigen
100%
T Antigen
75%
CD8+ Cells
18%
Immunization
12%
SV40 Large T Antigen
12%
Recombinant Vaccinia Virus
12%
Tumor
6%
Tumor Progression
6%
C57BL
6%
Minigene
6%
6 Months of Age
6%
Tumor Immunity
6%
Amylase
6%
CD4+ T Cells
6%
CTL Response
6%
Immunology and Microbiology
Epitope
100%
Cytotoxic T Cell
100%
Simian Virus 40
100%
Transgenic Mouse
100%
Virus Large T Antigen
100%
CD8+ Cell
13%
Vaccinia Virus
9%
Promoter Region
4%
Cell Line
4%
Syngenic
4%
C57BL 6 Mouse
4%
T-Helper Cell
4%
Tumor Immunity
4%
SV40 Large T Antigen
4%
Amylase
4%