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The role of granzyme B cluster proteases in cell-mediated cytotoxicity
Christine T.N. Pham
,
Timothy J. Ley
Division of Rheumatology
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
Institute of Clinical and Translational Sciences (ICTS)
Siteman Cancer Center
Center of Regenerative Medicine
Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
Department of Medicine
Division of Oncology
Section of Stem Cell Biology
Rheumatic Diseases Research Resource-Based Center
Division of Veterans Affairs
DBBS - Immunology
DBBS - Molecular Genetics and Genomics
DBBS - Cancer Biology
Research output
:
Contribution to journal
›
Article
›
peer-review
43
Scopus citations
Overview
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Keyphrases
Protease
100%
Granzyme B
100%
Cell Toxicity
100%
Cytotoxic Lymphocytes
100%
Graft-versus-host Disease (GvHD)
33%
Granzyme
33%
Induced Apoptosis
33%
CD4 Cells
33%
Cytotoxicity
33%
Perforin
33%
Lymphocyte Function
33%
Serine Protease
33%
Physiological Relevance
33%
B Locus
33%
CD8+ Cells
33%
Lytic Granules
33%
Biochemistry, Genetics and Molecular Biology
Cell Mediated Cytotoxicity
100%
Granzyme B
100%
Protease
100%
Lymphocyte
66%
Host
33%
CD4
33%
Cytotoxicity
33%
Serine Protease
33%
Granzyme
33%
Target Cell
33%
Lymphocyte Function
33%
CD8+ Cell
33%
Perforin
33%
Programmed Cell Death
33%
Immunology and Microbiology
Granzyme B
100%
Cell Mediated Cytotoxicity
100%
Cytotoxic Lymphocyte
100%
Target Cell
33%
CD4
33%
Granzyme
33%
Cytotoxicity
33%
Perforin
33%
Lymphocyte Function
33%
Acute Graft Versus Host Disease
33%
CD8+ Cell
33%
Programmed Cell Death
33%
Serine
33%