740 research outputs found

    Responsible Parenthood in the Writings of Pope Paul VI and Pope John Paul II

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    Lay Attorneys in the Tribunal

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    Lay Attorneys in the Tribunal

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    Development of an empirically based dynamic biomechanical strength model

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    The focus here is on the development of a dynamic strength model for humans. Our model is based on empirical data. The shoulder, elbow, and wrist joints are characterized in terms of maximum isolated torque, position, and velocity in all rotational planes. This information is reduced by a least squares regression technique into a table of single variable second degree polynomial equations determining the torque as a function of position and velocity. The isolated joint torque equations are then used to compute forces resulting from a composite motion, which in this case is a ratchet wrench push and pull operation. What is presented here is a comparison of the computed or predicted results of the model with the actual measured values for the composite motion

    Correlation and prediction of dynamic human isolated joint strength from lean body mass

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    A relationship between a person's lean body mass and the amount of maximum torque that can be produced with each isolated joint of the upper extremity was investigated. The maximum dynamic isolated joint torque (upper extremity) on 14 subjects was collected using a dynamometer multi-joint testing unit. These data were reduced to a table of coefficients of second degree polynomials, computed using a least squares regression method. All the coefficients were then organized into look-up tables, a compact and convenient storage/retrieval mechanism for the data set. Data from each joint, direction and velocity, were normalized with respect to that joint's average and merged into files (one for each curve for a particular joint). Regression was performed on each one of these files to derive a table of normalized population curve coefficients for each joint axis, direction, and velocity. In addition, a regression table which included all upper extremity joints was built which related average torque to lean body mass for an individual. These two tables are the basis of the regression model which allows the prediction of dynamic isolated joint torques from an individual's lean body mass

    Book Reviews

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    THE SUPREME COURT AND RELIGION. By Richard E. Morgan. New York: The Free Press, 1972. Pp. 216. 7.95.WHORUNSCONGRESS?THEPRESIDENT,BIGBUSINESS,ORYou?ByMarkJ.Green,JamesM.FallowsandDavidR.Zwick.NewYork:BantamBooksandGrossmanPublishers,1972.Pp.307.7.95. WHO RUNS CONGRESS? THE PRESIDENT, BIG BUSINESS, OR You? By Mark J. Green, James M. Fallows and David R. Zwick. New York: Bantam Books and Grossman Publishers, 1972. Pp. 307. 1.95. PRIVATE INTEREST AND PUBLIC GAIN: THE DARTMOUTH COLLEGE CASE, 1819. By Francis N. Stites. Amherst: The University of Massachusetts Press, 1972. Pp. 176. 9.50.JUSTICEISTHECRIME:PRETRIALDELAYINFELONYCASES.ByLewisR.Katz,withLawrenceB.LitwinandRichardH.Bamberger.Cleveland:CaseWesternReserveUniversityPress,1972.Pp.386.9.50. JUSTICE IS THE CRIME: PRETRIAL DELAY IN FELONY CASES. By Lewis R. Katz, with Lawrence B. Litwin and Richard H. Bamberger. Cleveland: Case Western Reserve University Press, 1972. Pp. 386. 6.95

    The Glucagon Receptor Is Required for the Adaptive Metabolic Response to Fasting

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    SummaryGlucagon receptor (Gcgr) signaling maintains hepatic glucose production during the fasting state; however, the importance of the Gcgr for lipid metabolism is unclear. We show here that fasted Gcgr−/− mice exhibit a significant increase in hepatic triglyceride secretion and fasting increases fatty acid oxidation (FAO) in wild-type (WT) but not in Gcgr−/− mice. Moreover fasting upregulated the expression of FAO-related hepatic mRNA transcripts in Gcgr+/+ but not in Gcgr−/− mice. Exogenous glucagon administration reduced plasma triglycerides in WT mice, inhibited TG synthesis and secretion, and stimulated FA beta oxidation in Gcgr+/+ hepatocytes. The actions of glucagon on TG synthesis and FAO were abolished in PPARα−/− hepatocytes. These findings demonstrate that the Gcgr receptor is required for control of lipid metabolism during the adaptive metabolic response to fasting
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