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br Acknowledgments This work was supported by the
2020-07-31
Acknowledgments This work was supported by the National Natural Science Foundation of China (21275003, 21505082), a project of Shandong Province Higher Educational Science and Technology Program (Grant J16LC10)and the Open Funds of the Shandong Province Key Laboratory of Detection Technology for
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Recent published data have shown that
2020-07-30
Recent published data have shown that enolase from Leptospira interrogans is secreted into the extracellular medium and then reassociates with the bacterial surface by interacting with outer membrane proteins [17]. Anti-enolase cpmt synthesis recognize intact, non-permeabilized leptospires, thus in
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casein kinase 2 inhibitor The central pyridine ring appeared
2020-07-30
The central pyridine ring appeared to be important for biological activity (). Substitution by a pyrimidine ring or phenyl ring – resulted in a decrease in DGAT-1 inhibition. These analogs were synthesized by the route depicted in using 2-chloro-5-nitropyrimidine, 1-fluoro-4-nitrobenzene, or 1,2-d
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DDR receptor effector mechanisms are not well understood
2020-07-30
DDR receptor effector mechanisms are not well understood. Most descriptions of DDR function have focused on downstream signaling pathways activated by collagen that regulate cell proliferation and transcriptional activation [7]. Natural occurring or induced DDR2−/− genotypes in mice induce dwarfism,
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To our knowledge neither in vivo nor in vitro inhibitions
2020-07-30
To our knowledge, neither in vivo nor in vitro inhibitions by potential flavones such as diosmin, naringenin, and naringin on the piscine CYP450 system have been studied. The European Food Safety Authority concluded, based on available information of naringin effects in target organisms, that its pr
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br Conclusions New and exciting evidence supports the propos
2020-07-30
Conclusions New and exciting evidence supports the proposal that both CRF1 and CRF2 receptors play a relevant role in CRF-dependent neuroadaptations determining stress-induced relapse to drug seeking behaviour. Fig. 1 depicts the basic neuronal circuit involved in stress-induced relapse to drug s
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To assess the involvement of the hydrocarbon
2020-07-30
To assess the involvement of the hydrocarbon chain of C75-CoA positioning in the acyl group binding pocket, we carried out C75-CoA inhibitory experiments with the new mutated protein, CrAT D356A/M564G. This protein has a deep T7 Tag Peptide pocket for the binding of long-chain instead of short-chai
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br Author contributions br Disclosure statement br Transpare
2020-07-30
Author contributions Disclosure statement Transparency document Acknowledgements This work is part of a research program, which is financed by the Province of Fryslân (01120657), the Netherlands and Alfasigma Nederland B.V (direct contribution to grant number 01120657). Introduction
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br Experimental br Acknowledgements This research was financ
2020-07-29
Experimental Acknowledgements This research was financially supported by the Scientific and Technological Developing Scheme of Jilin Province of People\'s Republic of China (20150101225JC). Introduction Obesity is a serious health risk signal characterized by excess accumulation of triglyc
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TrypanosomaParasitic protozoans have been extensively invest
2020-07-29
TrypanosomaParasitic protozoans have been extensively investigated due to the search for new effective drugs for the dangerous diseases they cause. Because mammalian mitochondria do not possess alternative dehydrogenase in the respiratory chain, these proteins have become a specific potential target
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Of importance to the present investigation two studies Carva
2020-07-29
Of importance to the present investigation, two studies (Carvalho-Netto et al., 2007, Litvin et al., 2007) investigated the role played by CRF receptors of the dorsal periaqueductal gray (dPAG), which express both subtypes of CRF ligand sites (Merchenthaler, 1984, Swanson et al., 1983), in the regul
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AON successfully alleviated the myotonic
2020-07-29
AON successfully alleviated the myotonic phenotype in DM model mice [18], [23]. To screen for an optimal AON sequence, we used 25-mer phosphorothioate 2′ O-methyl RNA molecules that covered the Urolithin A 6B or exon 7A. Unexpectedly, AON 7A (+63−8) which covers the boundary of intron 7A and exon 7
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Hedamycin isolated from Streptomyces griseoruber
2020-07-28
Hedamycin, isolated from Streptomyces griseoruber, belongs to the highly cytotoxic pluramycin class of TWS119 (Figure 3(c)). It consists of a planar anthrapyrantrione chromophore attached to two amino sugar rings at one end and a bisepoxide-containing side-chain at the other end (Figure 3(c)). Hedam
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We have reported previously that aminoacrylate derivatives o
2020-07-28
We have reported previously that β-aminoacrylate derivatives of the general structure () are inhibitors of DHODH. In particular, tricyclic derivatives and displayed sub-micromolar IC values against DHODH, and in the case of there was a 1000-fold greater potency compared to the human enzyme (DHOD
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The discoidin domain receptors DDR and DDR are
2020-07-28
The discoidin domain receptors, DDR1 and DDR2, are receptor tyrosine kinases that are activated by different types of collagen (Shrivastava et al., 1997, Vogel et al., 1997). Both receptors interact with a number of fibrillar collagens, and DDR1, but not DDR2, is also activated by the network-formin
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