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- BookYu-Kang Tu, Darren C. Greenwood, editors.Contents:
Confounding and causal path diagrams
Statistical modelling of partially observed data using multiple imputation: principles and practice
Measurement errors in epidemiology
Selection bias in epidemiologic studies
Multilevel modelling
Modelling data that exhibit an excess number of zeros : zero-inflated models and generic mixture models
Multilevel latent class modelling
Bayesian bivariate disease mapping
Multivariate random fraility effects model for multiple spatially dependent survival data
Meta-analysis of observational studies
Directed acyclic graphs and structural equation modelling
Latent growth curve models
Growth mixture modelling for life course epidemiology
G-estimation for accelerated failure time models
Generalised additive models
Regression and classification trees
Statistical interactions and gene-environment joint effects.Digital Access Springer 2012 - ArticleWolberg WH.Cancer Res. 1977 Oct;37(10):3711-9.Colonic tissue membrane binding to peripheral blood mononuclear leukocytes was quantitated by 125I labeling of membrane fragments and by determining the acquisition of membrane-specific enzyme activity and radioactivity in mononuclear cells after contact with the tissue membrane fragments. Mononuclear cells bound equal amounts of normal and tumor tissue membrane fragments. Mononuclear cells capable of binding homologous but not autologous colonic tissue membranes were recovered from the peripheral blood of colon cancer-bearing patients. Mononuclear cells capable of binding autologous colonic tissue membranes appeared in the peripheral blood of patients after curative but not palliative tumor resection. Tumor membrane enzymes, including alkaline phosphatase, were introduced to mononuclear cells by bound tissue fragments. The activity of alkaline phosphatase present in the bound membrane fragments was inhibited by the immunorestorative drug, levamisole. Cellular debris liberated from tumors may play an important role in overcoming the host's defenses by binding to mononuclear cells, saturating antigen-binding sites, and introducing exogenous enzymes.