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Blood, Vol. 107, Issue 5, 2200-2207, March 1, 2006 This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef Genetic variation in bactericidal/permeability-increasing protein influences the risk of developing rapid airflow decline after hematopoietic cell transplantation Blood Chien et al. 107: 2200 Supplemental materials for: Chien et al Files in this Data Supplement: Table S1. Haplotype tagging single nucleotide polymorphisms selected for 15 innate immunity genes (PDF, 44.4 KB) Table S2. Allelic analysis of patient and donor genotypes in multivariate models (PDF, 80.7 KB) - All analyses were conducted using multivariate models that included clinical variables previously identified to be associated with the development of significant airflow decline after hematopoietic cell transplant (age at transplant, pretransplant one-second forced expiratory volume, and extent of graft versus host disease). All models also included duration of follow-up as a covariate. Table S3. Summary of all haplotype data analysis for discovery cohort patients and donors (PDF, 43 KB) - All analyses were conducted using multivariate models that included clinical variables previously identified to be associated with the development of significant airflow decline after hematopoietic cell transplant (age at transplant, pretransplant one-second forced expiratory volume, and extent of graft versus host disease). All models also included duration of follow-up as a covariate. Haplotype numbers for BPI and LBP do not correlate with the numbers assigned in Tables 2-4. However, the haplotypes are the same. This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef

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