|
|
Blood, Vol. 110, Issue 7, 2235-2241, October 1, 2007
High-risk HLA allele mismatch combinations responsible for severe acute graft-versus-host disease and implication for its molecular mechanism
Blood Kawase et al.
110: 2235
Supplemental materials for Kawase et al, Vol. 110, Issue 7, 2235-2241
Files in this Data Supplement:
- Table S1. Patient charactaristics (PDF, 12.7 KB)
- Table S2. HLA alleles whose frequencies are over 5% in the Japanese population and less than 1% in white populations (PDF, 11.3 KB)
- Table S3. Positions of amino acid substitution and substituted amino acids in HLA-A (PDF, 13.6 KB)
- Table S4. Positions of amino acid substitution and substituted amino acids in HLA-B (PDF, 14 KB)
- Table S5. Positions of amino acid substitution and substituted amino acids in HLA-Cw (PDF, 18.1 KB)
- Table S6. Comparison of validating methods (PDF, 14.3 KB)
- Table S7. Multivariable analysis of impact of mismatch pairs for severe aGVHD in HLA-B, -DR, -DQ and -DP (PDF, 15.3 KB)
- Table S8. Factors affecting severe aGVHD and OS in multivariate analyis of impact of number of nonpermissive mismatches (PDF, 11.6 KB)
- Table S9. Multivariable analysis of impact for OS about aGVHD high-risk amino acid substitutions (PDF, 11.8 KB)
| |
