Predicting the MHC-Peptide Affinity Using Some Interactive-Type Molecular Descriptors and QSAR Models
Reference30 articles.
1. Watts, C. Capture and processing of exogenous antigens for presentation on MHC molecules. Annu. Rev. Immunol.
1997, 15, 821–850. 2. Rudensky, A.; Prestoa-Hurlburt, P.; Hong, S. C.; Barlow, A.; Janeway, C. A. Jr. Sequence analysis of peptides bound to MHC class II molecules. Nature
1991, 353, 622–627. 3. Chicz, R. M.; Urban, R. G.; Lone, W. S.; Gorga, J. C.; Stern, L. J.; Vignali, D. A.; Strominger, J. L. Predominant naturally processed peptides bound to HLA-DR1 are derived from MHC-related molecules and are heterogeneous in size. Nature
1992, 358, 764–768. 4. Tiwari, J.; Terasaki, P. HLA and disease association. Springer-Verlag, New York, 1985. 5. Rowley, M. J.; Stockman, A.; Bond, C. A.; Tait, B. D.; Rowley, G. L.; Sherritt, M. A.; Mackay, I. R.; Muirden, K. D.; Bernard, C. C. The effect of HLA-DRB1 disease susceptibility markers on the expression of RA. Scand. J. Rheumatol. 1997, 26, 448–455.
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