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Acknowledgment This work was supported by the Swedish
2019-07-12

Acknowledgment This work was supported by the Swedish Research Council, the Knut and Alice Wallenberg Foundation, the Göran Gustafsson Foundation, the Swedish Pain Relief Foundation, the Torsten Söderbergs Stiftelse, the Swedish Children\'s Cancer Foundation, and the Swedish Cancer Society. The
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br Materials and methods br Results br Discussion Persimmon
2019-07-12

Materials and methods Results Discussion Persimmon tannin has been reported to have the bile acid binding ability in vitro (Matsumoto et al., 2011) and hypolipidaemic effects in animals (Matsumoto et al, 2008, Zou et al, 2012). Our previous study also proved that persimmon tannin promoted t
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The quaternary structure of many of the family B members
2019-07-12

The quaternary structure of many of the family B members (i.e., secretin, glucagon, glucagon-like peptide and Ac-IETD-pNA of receptors) have been actively studied and it has been demonstrated that they can form homodimers/oligomers (Gao et al., 2009; Ng & Chow, 2015; Ng, Lee, & Chow, 2013). Harikuma
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Our study showed that parental morphine exposure in the adul
2019-07-12

Our study showed that parental morphine exposure in the adulthood is associated with an increased tendency toward morphine consumption in F1 but not F2 male offspring. Thus, it seems that trans-generational effects of parental morphine consumption disappear in the second generation. In support of ou
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In the horse oviduct the EP receptor was most
2019-07-12

In the horse oviduct, the EP2 receptor was most strongly expressed in epithelial TCS 5861528 particularly in nonciliated (secretory) epithelial cells as evidenced by IHC. Furthermore, relative amount of EP2 mRNA was greater in the ampulla than in the isthmus, although this likely reflects differenc
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In terms of its protease activity MME has a broad
2019-07-12

In terms of its protease activity, MME has a broad range of substrates being able to target glucagon, bradykinin, GLP1, and several other Fenoprofen Calcium of circulating small molecules [25]. MME has been shown to target free insulin B-chain [32], although whether MME could target and degrade the
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We have previously reported DAPK inhibitors discovered throu
2019-07-12

We have previously reported DAPK inhibitors discovered through our structure-based virtual screening (SBVS) research program. In this paper, we describe the general protocol of our in silico approach, and the strategy used to develop hit compounds. In addition, the studies conducted on the structure
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Key molecules in the EP second messenger signaling cascade t
2019-07-12

Key molecules in the EP1 second messenger signaling cascade that are necessary for potentiation of GluK2/GluK5 were identified. We also identified three GluK5 serines located in a membrane-proximal C-terminal domain that, when mutated to the phosphomimetic aspartate and expressed with GluK2, rendere
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Repulsive interactions towards undesirable substrates are
2019-07-12

Repulsive interactions towards undesirable substrates are arguably a very efficient means to implement specificity [8]. In particular, it could be assumed that discrimination against a substrate that is larger than the cognate substrate may be achieved easily by restricting the active site and explo
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Uracil residues incorporated into DNA exist transiently sinc
2019-07-12

Uracil residues incorporated into DNA exist transiently since they are subject to removal by the multi-step uracil-initiated DNA CGS 35066 excision repair (BER) process [2], [14]. In E. coli, uracil-DNA BER is initiated by uracil-DNA glycosylase (Ung), which catalyzes the hydrolytic cleavage of the
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Some studies have been conducted on the activities http www
2019-07-12

Some studies have been conducted on the activities of CYP450 [[28], [29], [30], [31]]. For example, Chen et al. reported that low-dose aspirin induced the in vivo activity of CYP2C19 in healthy subjects [30], Krasniqi et al. reported that CYP2C8*3 and CYP2C9*2*3 variants correlated with ibuprofen-in
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Activating GSK signaling to inhibit PK signaling
2019-07-11

Activating GSK3β signaling to inhibit PK signaling during ischemia/reperfusion (I/R) is protective of WM ischemic injury. Glycogen synthase kinase (GSK3), which was the first substrate identified for AKT [44], is inhibited by AKT phosphorylation at positions S9 and S21 [45]. When GSK3β is active, it
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Caspase-10/b, human recombinant protein Interestingly from
2019-07-11

Interestingly, from our consensus SBVC protocol only few compounds (less than 150) have been scored with a full ‘ consensus’. That means that these compounds appear in the top 5% of the database when ranked by every scoring function independently. After visual inspection, we have realized that two a
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The consistent anti anxiety effects obtained
2019-07-11

The consistent anti-anxiety effects obtained with intra-mPFC injections of CP 376395 strongly suggest a tonic role of CRF at CRF1 receptors located within this limbic neurokinin receptor antagonist area in the modulation of anxiety in the mouse on the EPM. Intra-mPFC injection of CP 376395 led mice
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br Materials and methods br Results br
2019-07-11

Materials and methods Results Discussion The EP4 ion channels for PGE2 is similar to the EP1, EP2 and EP3 receptors in that they all have seven transmembrane segments and are coupled to Gα subunits of heterotrimeric G proteins, with a different Gα subunit for each receptor (Sugimoto and Nar
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