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101.
T. Pech J. Fujishiro T. Finger I. Ohsawa M. Praktiknjo M. von Websky S. Wehner K. Abu-Elmagd J. C. Kalff N. Schaefer 《Langenbeck's archives of surgery / Deutsche Gesellschaft fur Chirurgie》2012,397(1):131-140
Purpose
Ischemia-reperfusion injury leads to impaired smooth muscle function and inflammatory reactions after intestinal transplantation. In previous studies, infliximab has been shown to effectively protect allogenic intestinal grafts in the early phase after transplantation with resulting improved contractility. This study was designed to reveal protective effects of infliximab on ischemia–reperfusion injury in isogenic transplantation. 相似文献102.
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G. Owen Schaefer Markus K. Labude 《Journal of assisted reproduction and genetics》2017,34(12):1577-1580
With the recent report of a live birth after use of mitochondrial replacement therapy, sometimes called ‘three-parent IVF’, the clinical application of the technique is fast becoming a reality. While the United Kingdom allows the procedure under regulatory scrutiny, it remains effectively outlawed in many other countries. We argue that such prohibitions may violate individuals’ procreative rights, grounded in individuals’ interest in genetic affinity. The interest in genetic affinity was recently endorsed by Singapore’s highest court, reflecting an emphasis on the importance of biological ties found across the globe. We apply that reasoning to make the case for a right to ‘three-parent IVF’. 相似文献
105.
J. D. Gomez-Mantilla U. F. Schaefer V. G. Casabo T. Lehr C. M. Lehr 《The AAPS journal》2014,16(4):791-801
Appropriate setting of dissolution specification of extended release (ER) formulations should include precise definition of a multidimensional space of complex definition and interpretation, including limits in dissolution parameters, lag time (t-lag), variability, and goodness of fit. This study aimed to set dissolution specifications of ER by developing drug-specific dissolution profile comparison tests (DPC tests) that are able to detect differences in release profiles between ER formulations that represent a lack of bioequivalence (BE). Dissolution profiles of test formulations were simulated using the Weibull and Hill models. Differential equations based in vivo–in vitro correlation (IVIVC) models were used to simulate plasma concentrations. BE trial simulations were employed to find the formulations likely to be declared bioequivalent and nonbioequivalent (BE space). Customization of DPC tests was made by adjusting the delta of a recently described tolerated difference test (TDT) or the limits of rejection of f2. Drug k a (especially if k a is small), formulation lag time (t-lag), the number of subjects included in the BE studies, and the number of sampled time points in the DPC test were the factors that affected the most these setups of dissolution specifications. Another recently described DPC test, permutation test (PT), showed excellent statistical power. All the formulations declared as similar with PT were also bioequivalent. Similar case-specific studies may support the biowaiving of ER drug formulations based on customized DPC tests. 相似文献
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Stephen Murphy James Smadbeck Bruce Eckloff Yean Lee Sarah Johnson Giannoula Karagouga Vishnu Serla Anurag Sharma Robert Sikkink Jesse Voss Faye Harris Janet Schaefer Kline Farhad Kosari Andrew Feldman Eric Wieben Marie Christine Aubry Benjamin Kipp Jin Jen George Vasmatzis 《The Journal of molecular diagnostics : JMD》2021,23(4):375-388
108.
Factors Associated with Reported Infection and Lymphedema Symptoms among Individuals with Extremity Lymphedema 下载免费PDF全文
Jie Deng PhD RN OCN Mei R. Fu PhD RN APRN‐BC FAAN Jane M. Armer PhD RN FAAN Janice N. Cormier MD MPH M. Elise Radina PhD CFLE Saskia R.J. Thiadens RN Jan Weiss PT DHS CLT‐LANA Catherine M. Tuppo PT MS CLT‐LANA Mary S. Dietrich PhD Sheila H. Ridner PhD RN FAAN 《Rehabilitation nursing》2015,40(5):310-319
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