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  • Book
    Anthony G. Gallagher, Gerald C. O'Sullivan.
    Contents:
    Agents of Change
    Simulations for Procedural Training
    Human Factors in Acquiring Medical Skill; Perception and Cognition
    Human Factors in Acquiring Medical Skills; Learning and Skill Acquisition in Surgery
    Metrics for the Measurement of Skill
    Metric-Based Simulation Training
    Validation of Metrics Coupled to Simulation Training
    Metric-Based Training to Proficiency: What Is It and How Is It Done?
    Didactic Education and Training for Improved Intraoperative Performance: e-Learning Comes of Age
    Simulation Training for Improved Procedural Performance
    Simulation In and For Medicine: Where Next?
    Proficiency-Based Progression Simulation Training: A To-Do List for Medicine.
    Digital Access Springer 2012
  • Article
    Ramseier H, Lindenmann J.
    Exp Cell Biol. 1977;45(1-2):101-17.
    The product of antigenic recognition (PAR) is an antigen-antibody complex with granulotactic activity. The following results support his conclusion. PAR generated by cell-bound or shed T-cell RS or the recognizing structure of T alloantisera and alloantigen can be destroyed by heating at 56 degrees C for 30 min, because of inactivation of a heat-labile component supplied by alloantigen. Recognizing partners of these complexes are heat-stable. They form PAR anew when alloantigen is added or upon confrontation with anti-RS serum. They are also capable of inducing anti-RS sera. PAR preparations composed of these recognizing structures and antibodies to them are heat-inactivated at much higher temperatures, because both partners of the complex are relatively heat-stable. Heat-labile PAR complexes (recognizing structures and alloantigen) pass anti-mouse immunoglobulin immunosorbent, but are retained specifically by alloantiserum (via alloantigen of the complex) or by anti-RS serum (via RS of the complex) bound to the column.
    Digital Access Access Options