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Biomedical subjects

D J Stekel

Publications and source records attributed to D J Stekel.

6 recordsLinked to original sources

The comparison of gene expression from multiple cDNA libraries.

We describe a method for comparing the abundance of gene transcripts in cDNA libraries. This method allows for the comparison of gene expression in any number of libraries, in a single statistical analysis, to identify differentially expressed genes. Such genes may be of potential biological or pharmaceutical relevance. The formula that we derive is essentially the entropy of a partitioning of genes among cDNA libraries. This work goes beyond previously published analyses, which can either compare only two libraries, or identify a single outlier in a group of libraries. This work also addresses the problem of false positives associated with repeating the test on many thousands of genes. A randomization procedure is described that provides a quantitative measure of the degree of belief in the results; the results are further verified by considering a theoretically derived large deviations rate for the test statistic. As an example, the analysis is applied to four prostate cancer libraries from the Cancer Genome Anatomy Project. The analysis identifies biologically relevant genes that are differentially expressed in the different tumor cell types.

Gene Expression Profiling↗

The simulation of density-dependent effects in the recirculation of T lymphocytes.

T-lymphocyte recirculation appears to be slower in nude or irradiated rats as compared with normal rats. A mathematical model of T-lymphocyte recirculation that incorporates interactions between T cells and dendritic cells in the lymphoid tissue is presented. It is shown that these interactions are able to explain the differences in recirculation times between normal and nude or irradiated rats, and also the time-scales seen in long-term thoracic duct cannulations.

Animals↗

The role of inter-cellular adhesion in the recirculation of T lymphocytes.

We refine an existing model of T lymphocyte recirculation, in order to incorporate a description of the adhesion between T cells and other cell types in the lymphoid tissue, such as dendritic cells. The new model is able to fit the animal experiments on lymphocyte recirculation. It also allows for the variation of these adhesive properties, as would occur in the presence of antigen, and it is shown that it is possible for the T cell counts in blood to reach very low levels, as a result of increased adhesion between T cells and dendritic or other cells present in the lymphoid tissue. We discuss the implications of this phenomenon for HIV infection.

Animals↗

Antigenic diversity thresholds and hazard functions.

In this paper, we answer some points made in a recent paper by N.I. Stilianakis and coworkers on the antigenic diversity threshold model for acquired immune deficiency syndrome pathogenesis. An extended version of the model is then used to compute hazard functions for the human immunodeficiency virus incubation period that are in agreement with empirically observed hazard functions.

Acquired Immunodeficiency Syndrome↗