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br Experimental section br Acknowledgment S
2024-10-14
Experimental section Acknowledgment S.B.T. is grateful to the Deutsche Forschungsgemeinschaft (DFG), the Wilhelm Sander-Stiftung and Interdisciplinary Center for Molecular Materials (ICMM) for generous research support. M.M. greatly acknowledges the experimental support and the scientific cont
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Interestingly we found that co treatment with
2024-10-14
Interestingly, we found that co-treatment with losartan prevented the increased participation of ROS from NADPH oxidase on the contractile response to Phe observed in Hg-treated rats. Moreover, losartan also prevented the reduction in the endothelial NO modulation of this response found in treated a
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Androgen receptor translocates from the cytoplasm
2024-10-14
Androgen receptor translocates from the cytoplasm to the nucleus after binding to its ligands (Quigley et al., 1995). In the current study, although propofol did not significantly affect total androgen receptor protein levels, it significantly decreased nuclear androgen receptor levels. These findin
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WKY and SHR strains have important
2024-10-14
WKY and SHR strains have important differences mainly in their sympathetic status but also in the activity of the RAS. The development of hypertension in SHR is clearly related to an increase in sympathetic activity [51], [11]. In addition, increased renal sympathetic nerve activity led to an increa
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A unique finding in this study is
2024-10-14
A unique finding in this study is that 12/15-LO influences CREB phosphorylation in the murine brain. While previous reports have found that knockout of 5-lipoxygenase, a related enzyme that also uses arachidonic Ryuvidine for substrate, can regulate CREB phosphoryation in the context of Alzheimer's
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The complex role of the
2024-10-14
The complex role of the human intestinal microbiota is emerging and its functions has been elucidated when considering energy metabolism, nutrient digestion, vitamin synthesis, epithelial defenses and immune responses [34]. The colon is responsible for salvage of energy and possibly nitrogen from ca
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Similarly compound was prepared from aldehyde
2024-10-14
Similarly, THZ2 13 was prepared from aldehyde 8d by following similar procedures (Scheme 3). Condensation of 13 with 7b or 7e provided the corresponding amides 9j or 9k, which then went through O-debenzylation by BCl3 to deliver the final compounds 10j and 10k in 37% and 32% overall yields, respect
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The AHR potentially enhances IDO expression possibly
2024-10-14
The AHR potentially enhances IDO-expression, possibly via crosstalk with several inflammatory signaling pathways (shown by now for IL6 and ‘signal transducer and activator of transcription’ (STAT) 3, and for NFκB, toll like receptor-pathways) [56,59,60]. IDO metabolizes Trp to kynurenines, which are
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br Conclusion br Conflict of interest br Acknowledgments We
2024-10-14
Conclusion Conflict of interest Acknowledgments We thank Nancy Kerkvliet for helpful advice. The research in the lab of CE and THS is supported by the Deutsche Forschungsgemeinschaft (grants ES103/7-1 and 9-1, HA7346/2-1). We apologize to all authors whose work could not be cited due to lim
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Derivatives of M that possess either an
2024-10-12
Derivatives of (+)-M100907 that possess either an alkyne or an azide have been synthesized. The most active enantiomer was obtained by resolution of a relatively early intermediate in the synthesis. The ability of these stock aee to maintain 5-HTR antagonist properties as (+)-M100907 was demonstrat
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Hexa His We aim to evaluate the AK in regulating adenosine s
2024-10-12
We aim to evaluate the AK in regulating adenosine signaling in the retina. It was reported that the degree of Hexa His injury directly depends on expression levels of AK and the resulting extracellular levels of adenosine (Boison, 2006). Indeed, transgenic mice overexpressing AK are highly suscepti
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Tension within the network could be explained by two potenti
2024-10-12
Tension within the network could be explained by two potential mechanisms: the more classical contractility that is dependent on motor proteins that are pulling SB 239063 mg filaments towards each other [10]; or contractility that is caused by disassembly of a crosslinked network of actin filaments
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Several tertiary prevention studies are currently
2024-10-12
Several tertiary prevention studies are currently underway examining the use of dutasteride for prostate cancer treatment: (1) during expectant management of prostate cancer, (2) after radical prostatectomy in men at high risk for relapse, and (3) in men with metastatic disease. The Reduction by Dut
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Because LTs are proved to mediate
2024-10-12
Because LTs are proved to mediate multiple biological and pathological responses in various disease states, the 5-LO biosynthetic pathway producing LTs from AA have been the target of drug discovery efforts for over two decades. As observed from literature, a pile of research efforts has been direct
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During the year study period of men in the dutasteride
2024-10-12
During the 4-year study period, 19.9% of men in the dutasteride group developed prostate cancer as compared to 25.1% in the placebo group, which represents an absolute risk 193 2 of 5.1% for men taking dutasteride (P the two groups at the 4 year end-point. The REDUCE study also examined the effects
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