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Another research group assessed pairs of middle aged years a
2024-05-28

Another research group assessed 8503 pairs of middle-aged (SB742457 the twin exposed to surgery had lower scores on cognitive tests in 49% of the pairs. Twins aged 70 and older who underwent hip and knee arthroplasty scored higher on cognitive tests, even higher than those who had not undergone any
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The cavity volume of the binding pocket may
2024-05-28

The cavity volume of the binding pocket may differ not only between species but also among various AhR/ARNT isoforms within a single species. It is noteworthy that even a single amino BML-277 substitution within a binding pocket may result in a change in the cavity volume. This, in turn, may affect
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In conclusion we have shown that mGlu receptors negatively
2024-05-28

In conclusion, we have shown that mGlu7 receptors negatively regulate α1-adrenergic receptor signalling in heterologous expression systems, Sitafloxacin tissue and living animals. This interaction might represent a protective mechanism aimed at restraining an excessive activation of noradrenergic tr
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br Methods br Results br Discussion Chronic stress renders i
2024-05-28

Methods Results Discussion Chronic stress renders individuals vulnerable to diseases, and this effect might be, at least partially, mediated by stress hormone-induced immunosuppression. Therefore, investigating the effects of catecholamines on immune SB 239063 is of high relevance. We hypo
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Vortioxetine is a multimodal antidepressant that acts as an
2024-05-28

Vortioxetine is a multimodal antidepressant that acts as an inhibitor at the serotonin (5-HT) transporter (SERT), an agonist at 5-HT1A receptors, a partial agonist at 5-HT1B receptors, and an antagonist at 5-HT1D, 5-HT3 and 5-HT7 receptors (Bang-Andersen et al., 2011, Sanchez et al., 2015). Based on
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br Functional consequences of ADK regulation on
2024-05-28

Functional consequences of ADK regulation on astrocyte function As outlined above (see introduction), ADK critically regulates the extracellular adenosine levels in nucleoside analog (Boison, 2006, Etherington et al., 2009). Changes in the levels of adenosine, as a result of the regulation of AD
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Previous studies have demonstrated the presence of soluble
2024-05-28

Previous studies have demonstrated the presence of soluble NTPDases, 5′-nucleotidase and adenosine deaminase in rat blood serum as well as in human blood (Doleski et al., 2016; Oses et al., 2004; Yegutkin, 1997; Yegutkin et al., 2007). In addition, our earlier reports have shown that these membrane-
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br STAR Methods br Author Contributions br Acknowledgments W
2024-05-28

STAR★Methods Author Contributions Acknowledgments We thank Antony M. Dean for initial discussions and encouragement concerning ancestral sequence reconstruction. We also thank Natalie K. Goto for constructive criticism concerning the manuscript, Steven M. Sine for providing csf1r receptor
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Fig A shows a schematic
2024-05-28

Fig. 2A shows a schematic representation of histological results according to the Franklin and Paxinos Mouse Brain Atlas (2001). The black circles represent the sites of drug infusion that were on-target within the amygdala. Gray circles represent the animals that had infusion locations outside the
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The synthesis and secretion of adrenal androgens
2024-05-28

The synthesis and secretion of adrenal androgens is apparently unique to humans and nonhuman primates, and requires the expression of key mediators such as CYP17 [26]. Endocrine control of CYP17 expression in rhesus monkeys is comparable to that in humans [27]. An analysis of baboon cDNA for CYP17 s
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Cholesterol sale The synthetic route for the
2024-05-28

The synthetic route for the aminobenzoxazole scaffold with a solvent accessible moiety is described in . Nitration of methoxyphenol and subsequent hydrogenation of the resulting nitro Cholesterol sale afforded compound . Aminobenzoxazole was formed by the reaction of compound with BrCN in EtOH. T
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Two major categories of arginase inhibitors have been
2024-05-27

Two major categories of arginase inhibitors have been distinguished (Fig. 3): the first category comprises synthetic arginase inhibitors, which have been developed from the substrate l-arginine [35]; and the second category includes inhibitors derived from natural products [36]. The category of synt
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br Consequences of central apelin APJ modulation Regarding e
2024-05-27

Consequences of central apelin/APJ modulation Regarding extra-hypothalamic actions, recent data demonstrate that the central apelin/APJ system could be a potential new target for the regulation of memory (Han et al., 2014). Then, intracerebroventricular (icv) apelin administration in mice impairs
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Apelin is a bioactive peptide and endogenous ligand for the
2024-05-27

Apelin is a bioactive peptide and endogenous ligand for the APJ receptor (APLNR), a member of the G protein coupled receptor family that shares a similar sequence as the angiotensin type-1 receptor (AT1) [5]. Early studies demonstrated that the apelin/APLNR receptor axis plays a significant role in
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Phenolic compounds show reciprocal relationship with colonic
2024-05-27

Phenolic compounds show reciprocal relationship with colonic microflora. Phenolic compounds are able to improve colonic health and modulate microbiota diversity with prebiotic and antimicrobial functions, while colonic bacterial enzymes catalyze deconjugation, dehydroxylation, and convert phenolic c
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