An analysis of the physical properties of peptides that influence the pigeon cytochrome c specific T lymphocyte response
- 11 November 1989
- journal article
- research article
- Published by Elsevier in Molecular Immunology
- Vol. 26 (11) , 1069-1079
- https://doi.org/10.1016/0161-5890(89)90071-0
Abstract
No abstract availableFunding Information
- W. W. Smith Charitable Trust
- National Institutes of Health (GM 3 1841)
This publication has 41 references indexed in Scilit:
- Correlation between computed conformational properties of cytochrome c peptides and their antigenicity in a T‐lymphocyte proliferation assayBiopolymers, 1987
- Generation of diversity in T cell receptor repertoire specific for pigeon cytochrome c.The Journal of Experimental Medicine, 1987
- A new T helper cell specificity within the pigeon cytochromec determinant 95–104European Journal of Immunology, 1987
- Design, synthesis, and characterization of a model peptide having potent calcitonin-like biological activity: implications for calcitonin structure/activityBiochemistry, 1985
- Rapid purification of radioiodinated peptides with Sep‐Pak® reversed phase cartridges and HPLCInternational Journal of Peptide and Protein Research, 1984
- Amphiphilic Secondary Structure: Design of Peptide HormonesScience, 1984
- Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing.The Journal of Experimental Medicine, 1983
- The fine specificity of antigen and la determinant recognition by T cell hybridoma clones specific for pigeon cytochrome cCell, 1982
- The T lymphocyte response to cytochrome c—II.: Molecular characterization of a pigeon cytochrome c determinant recognized by proliferating T lymphocytes of the B10.a mouseMolecular Immunology, 1980
- T-lymphocyte response to cytochrome c. I. Demonstration of a T-cell heteroclitic proliferative response and identification of a topographic antigenic determinant on pigeon cytochrome c whose immune recognition requires two complementing major histocompatibility complex-linked immune response genes.The Journal of Experimental Medicine, 1979