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The beneficial effects of IP on liver I-R injury seem to be a consequence of autophagy onset leading to preserved ATP levels and avoiding hepatocellular necrosis by delaying proapoptotic effects [ 29].
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At this point, more empirical research is needed by economists and sociologists, one way or another, to determine the effects of IP protection on technological and artistic development.
However, the literature on effects of IP-TFA on health has been consistent, and several studies have suggested that higher doses of IP-TFA are associated with increased risk of CVD.
The effects of IP administration of various chemotherapeutic agents on intestinal anastomotic wound healing have been investigated in many studies and the results have been conflicting [ 12- 16, 16, 24, 27, 28]; some have shown detrimental effects [ 12, 28].
Our aim in the present study was to investigate the effects of IP MTC, administered at various times postoperatively, on intestinal anastomotic wound healing.
The aim of this study was to investigate the effects of IP and IP associated with subanesthetic S-ketamine on renal function and histology in rats.
The present study investigated the effects of IP and IP associated with subanesthetic S-ketamine in ischemia-reperfusion-induced AKI.
This indicated no major effect of Ip overexpression on mHtt aggregation (Supplementary Material, Fig. S2).
The present study was designed to investigate the effects of beraprost sodium (BPS, an agonist of IP) on chronic brain injury and to primary explore neuroprotective mechanism of BPS through detecting the change of hippocampal neuronal PGI2 content, and the expressions of PGIS and IP at mRNA and protein levels in chronic aluminum-overload rats.
Open image in new window Fig. 4 a Effect of Ip and Ton on SR at Toff: 40 μs; SV 40 V, b effect of Toff and Ip on SR at Ton:112 µs; SV: 40 V, c effect of Ton and SV on SR at Ip: 120 A; Toff: 40 µs Open image in new window Fig. 5 a WEDM machined surface at Ip:150 A; Ton: 118 μs; Toff: 35 μs; SV: 30 V, b WEDM machined surface at Ip: 90 A; Ton: 106 μs; Toff: 50 μs; SV: 50 V.
The effect of IP contrast agent on residence times in the TD method will be considered in future studies.
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