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Cinchonidine In vertebrates three cognate receptors or recep
2021-09-27

In vertebrates, three cognate receptors or receptor-like sequences have been identified with distinct distributions and functions (Millar, 2005, Neill et al., 2001). Only two types of GnRHR occur in mammals, though (Morgan and Millar, 2004). The mammalian type I GnRHR shares over 80% amino Cinchonid
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P gps expressed in cells and
2021-09-27

P-gps, expressed in iCRT 14 and tissues of human and animals, play an active role in cellular protection against multiple toxicants by transporting them out of a cell. Thus, improving transport activity of P-gp may contribute to removing Cd from living oysters. Cd accumulation in the cultured cells
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Finally it is possible that the increase
2021-09-27

Finally, it is possible that the increase in the number of EAAT-3-labelled cells in the DG at PD 60, when compared with the control and experimental animals at PD 14, is associated with natural changes in the number of neurons present during the postnatal development of the hippocampus (41, 42) and,
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br Materials and Methods br
2021-09-27

Materials and Methods Results Discussion A model of seizure and excitotoxicity induced by neonatal MSG administration was described recently (19) in which extracellular glutamate increased after the first and second MSG administrations were observed, the greatest increase seen following the
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Here we showed that microinjection
2021-09-26

Here we showed that microinjection of siRNA at the MII stage efficiently reduced endogenous EZH2 mRNA and protein. Although the percentage of cleaving embryos was not affected, Memantine hydrochloride australia formation and blastocyst cell number were both reduced in EZH2 knockdown groups (Table 1
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The NVC response in the diseased or aging brain may
2021-09-26

The NVC response in the diseased or aging mibefradil may be altered, including changes in both the chemical mediators of NVC, ion channel behaviour, and the dynamics of the vascular system. For example, in Alzheimer’s disease the production of NO is shown to be inhibited (Lourenço et al., 2014), hy
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Activation of FXR or TGR inhibits inflammatory response via
2021-09-26

Activation of FXR or TGR5 inhibits inflammatory response via repressing NF-κB activity [1]. FXR is not expressed or expressed at a very low level in macrophages [45] (data not shown), but highly expressed in hepatocytes. In contrast, TGR5 is expressed in macrophages but not in hepatocytes. Our data
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From a cell signaling perspective given the importance of ag
2021-09-26

From a cell signaling perspective, given the importance of agonist-directed signaling and biased agonism, one goal of this research update was to review the known contributions of G protein-dependent versus β-arrestin-dependent signals toward promotion of beneficial functions that FFA4 facilitates.
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Another level of complexity within
2021-09-26

Another level of complexity within the TGF-ß/SMAD and Hippo/YAP/TAZ pathway crosstalks was recently uncovered. TGF-ß induces robust TAZ, but not YAP, protein expression in both mesenchymal and epithelial Terbinafine through a SMAD3-independent, p38/MAPK-dependent mechanism that triggers myocardin-r
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Several studies have proposed that high levels of KYNA in
2021-09-24

Several studies have proposed that high levels of KYNA in the Vincristine synthesis contribute to cognitive dysfunctions presented by patients who suffer from schizophrenia [30], [31], [32], [33]. Considering that: (i) KYNA is a known GPR35 agonist [2], (ii) cognitive impairments in patients with sc
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br Conflict of interest statement br Acknowledgments The
2021-09-24

Conflict of interest statement Acknowledgments The authors would like to thank Dr. Linda Console-Bram for her editing of this review, Valentina Lucchesi for help with the figures, and acknowledge funding from NIH/NIDA (DA023204). GPR35 is an orphan G protein-coupled receptor (GPCR) implicat
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Epiberberine It is interesting to note
2021-09-24

It is interesting to note that the long and short forms of GPR120 exist at different basal levels of phosphorylation, with the short form demonstrating a greater degree of constitutive activity [12]. Importantly, Burns and Moniri [12] showed that, upon activation, the long and short isoforms of GPR1
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Recently the novel fatty acid
2021-09-24

Recently, the novel fatty metforman receptor, GPR120 (also called FFAR4), has been shown to be implicated in diverse physiological homeostasis, such as insulin sensitization, anti-inflammation and regulation of appetite (Hirasawa et al., 2005, Oh et al., 2010). Notably, it is abundantly expressed i
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br Introduction High dose niacin or nicotinic acid has
2021-09-24

Introduction High dose niacin, or nicotinic acid, has been used as an athero-protective drug for more than 50 years (Carlson, 2005, Offermanns, 2006). When taken in pharmacological doses (>1g/day), the nicotinic Probucol form of niacin modulates plasma lipid profiles including decreasing circula
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The inhibition of NSAIDs towards GLOI provides a direction f
2021-09-24

The inhibition of NSAIDs towards GLOI provides a direction for the development of novel effective GLOI inhibitors. Although the inhibitory activity of indomethacin was determined and the interactions between it mm stock and GLOI were probed by NMR titration experiments, no detailed inhibitory mecha
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