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Results from current homology-based search tools, designed to locate biologically relevant sequences, present a level of uncertainty from an intellectual property standpoint.
T cells genetically modified to express a peptide–MHC complex, normally involved in the induction of autoimmunity, can kill pathogenic T cells and inhibit autoimmune disease.
The recently determined high-resolution crystal structure of the bacterial multidrug resistance transporter AcrB brings us one step closer to the design of more effective therapeutic agents.
Integration of variegated pharmaceutical data sets is a highly desirable goal, but attaining it requires more than placing all the data on the same server.