University of Wisconsin-Madison

About: University of Wisconsin-Madison is a education organization based out in Madison, Wisconsin, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 108707 authors who have published 237594 publications receiving 11883575 citations.

Directed assembly of block copolymer blends into nonregular device-oriented structures.

Abstract: Self-assembly is an effective strategy for the creation of periodic structures at the nanoscale. However, because microelectronic devices use free-form design principles, the insertion point of self-assembling materials into existing nanomanufacturing processes is unclear. We directed ternary blends of diblock copolymers and homopolymers that naturally form periodic arrays to assemble into nonregular device-oriented structures on chemically nanopatterned substrates. Redistribution of homopolymer facilitates the defect-free assembly in locations where the domain dimensions deviate substantially from those formed in the bulk. The ability to pattern nonregular structures using self-assembling materials creates new opportunities for nanoscale manufacturing.

An Attempted Integration of the Literature on the Export Behavior of Firms

Abstract: Forty-three studies on the export behavior of firms involving eleven countries were assembled. (The author believes that they constitute nearly all of the available literature on the subject.) An attempt was made to integrate them into a more-or-less meaningful whole that both yields interesting implications and provides a useful background guide for future research on the subject.

Quantifier elimination for real closed fields by cylindrical algebraic decomposition

Abstract: Tarski in 1948, (Tarski 1951) published a quantifier elimination method for the elementary theory of real closed fields (which he had discovered in 1930). As noted by Tarski, any quantifier elimination method for this theory also provides a decision method, which enables one to decide whether any sentence of the theory is true or false. Since many important and difficult mathematical problems can be expressed in this theory, any computationally feasible quantifier elimination algorithm would be of utmost significance.

Organization-Based Self-Esteem: Construct Definition, Measurement, And Validation

Abstract: The article introduces the construct “organization-based self-esteem” and its measurement. We developed a partial nomological network resulting in a set of hypotheses that guided efforts to validat...

CTLA4-Ig and anti-CD40 ligand prevent renal allograft rejection in primates

Abstract: Selective inhibition of T cell costimulation using the B7-specific fusion protein CTLA4-Ig has been shown to induce long-term allograft survival in rodents. Antibodies preventing the interaction between CD40 and its T cell-based ligand CD154 (CD40L) have been shown in rodents to act synergistically with CTLA4-Ig. It has thus been hypothesized that these agents might be capable of inducing long-term acceptance of allografted tissues in primates. To test this hypothesis in a relevant preclinical model, CTLA4-Ig and the CD40L-specific monoclonal antibody 5C8 were tested in rhesus monkeys. Both agents effectively inhibited rhesus mixed lymphocyte reactions, but the combination was 100 times more effective than either drug alone. Renal allografts were transplanted into nephectomized rhesus monkeys shown to be disparate at major histocompatibility complex class I and class II loci. Control animals rejected in 5–8 days. Brief induction doses of CTLA4-Ig or 5C8 alone significantly prolonged rejection-free survival (20–98 days). Two of four animals treated with both agents experienced extended (>150 days) rejection-free allograft survival. Two animals treated with 5C8 alone and one animal treated with both 5C8 and CTLA4-Ig experienced late, biopsy-proven rejection, but a repeat course of their induction regimen successfully restored normal graft function. Neither drug affected peripheral T cell or B cell counts. There were no clinically evident side effects or rejections during treatment. We conclude that CTLA4-Ig and 5C8 can both prevent and reverse acute allograft rejection, significantly prolonging the survival of major histocompatibility complex-mismatched renal allografts in primates without the need for chronic immunosuppression.