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Alloreactive and syngeneic CTL are comparably dependent on interaction with MHC class I α-helical residues
Tara M.C. Hornell
, Joyce C. Solheim
, Nancy B. Myers
,
William E. Gillanders
, Ganesaratnam K. Balendiran
, Ted H. Hansen
, Janet M. Connolly
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
Institute of Clinical and Translational Sciences (ICTS)
Siteman Cancer Center
Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
Section of Surgical Oncology
DBBS - Immunology
Research output
:
Contribution to journal
›
Article
›
peer-review
17
Scopus citations
Overview
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Dive into the research topics of 'Alloreactive and syngeneic CTL are comparably dependent on interaction with MHC class I α-helical residues'. Together they form a unique fingerprint.
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Keyphrases
Syngeneic
100%
Alloreactive
100%
MHC Class I
100%
Autoreactive T Cells
100%
T Cells
60%
Alloantigen
60%
MHC Alleles
40%
T Cell Clone
40%
Thymus
20%
T Cell Response
20%
High Affinity
20%
T Cell Recognition
20%
MHC Molecules
20%
Interface Residues
20%
Allotype
20%
Specific T Cells
20%
Recognition Pattern
20%
Primary Contact
20%
Immunology and Microbiology
T Cell
100%
Syngenic
100%
MHC Class I
100%
Alloreactive T Cell
83%
Allele
33%
Cell Clone
33%
Alloantigen Recognition
33%
Thymus
16%
T Cell Receptor
16%
Target Cell
16%
Alloantigen
16%
Allotype
16%
Pattern Recognition
16%