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br Molecular modeling simulation study Molecular modeling st
2019-09-10

Molecular modeling simulation study Molecular modeling study was performed through docking of the test compounds into the binding site of hDHFR enzyme using Discovery Studio 2.5 software. Computational docking is an algorithm designed to determine the suitable position and the orientation of the
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One possible explanation for differences
2019-09-10

One possible explanation for differences in the binding ability of monomeric versus dimeric forms of DDR2 ECD to collagen could be that the monomeric form only binds to the primary GVMGFO site, whereas dimeric (and oligomeric) DDR2 ECD binds to additional sites on the collagen triple-helical molecul
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br Acknowledgements br This work was supported by grants fro
2019-09-10

Acknowledgements This work was supported by grants from the National Natural Science Foundation of China (Grant No.: 30260088) and the prophase research for National “973” Project of China (Grant No.: 2007CB116203). The DNA sequences of Hbvp1 and the Hbvp1 promoter were deposited in GenBank, an
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br Contributors br Acknowledgements br
2019-09-10

Contributors Acknowledgements Introduction Pemphigus disorders are characterized by autoantibodies binding to desmosomes between epidermal cells, resulting in the loss of cell to cell adhesion and blister formation. In pemphigus foliaceus, autoantibodies predominantly bind to desmoglein 1,
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The CysLT receptor antagonist BayCysLT RA significantly
2019-09-10

The CysLT2 receptor antagonist BayCysLT2RA significantly suppressed multiple antigen challenge-induced infiltration of eosinophils and mononuclear Nitrotetrazolium Blue chloride pathway into the lung, indicating that CysLT2 receptor activation is involved in leukocyte migration. In contrast to the p
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br Diverse functions of ERK pathway Same as
2019-09-10

Diverse functions of ERK pathway Same as the other MAPK cascades, the ERK pathway is activated by several extracellular stimuli and different internal routes. ERK vitally tunes the function of various substrates in all cellular components; the nucleus, cytoplasm, membranes and the cytoskeleton. E
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br Transparency document br Introduction The cyclic nucleoti
2019-09-10

Transparency document Introduction The cyclic nucleotide adenosine 3′,5′-cyclic monophosphate (cAMP) exerts both an endothelium-dependent and an endothelium independent vasorelaxant action in rat Triciribine [1]. cAMP direct, endothelium-independent vasorelaxant effects have been attributed t
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br Results and discussion br Conclusion Recent
2019-09-10

Results and discussion Conclusion Recent studies showed that EGFR signaling is involved in inflammatory response in several inflammatory conditions. The normal inflammatory macrophage Brilliant Blue G show EGFR-dependent production of inflammatory mediators. Nevertheless, the development of E
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In contrast to AChE BuChE Table
2019-09-09

In contrast to AChE, BuChE (Table 2) exhibited a measurable time-dependent inactivation only with Isochlorogenic acid A 2 among the four acetophenones in this study. Values of Ki obtained from steady-state inhibition of BuChE by all four acetophenones were, as noted in the Results, 10- to 200-fold
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Phenylbenzofurans are a very important molecule skeleton due
2019-09-09

Phenylbenzofurans are a very important molecule skeleton due to their synthetic versatility and their proved pharmacological properties [2]. They are synthetic compounds in which an additional phenyl ring is present in any position of the benzofuran nucleus. This could be easily obtained possible by
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It is of interest to point
2019-09-09

It is of interest to point out that curcumin in this study reduced body weight gain; the underlying mechanism may be due to a decrease in general luteolin of fat, which was associated with a significantly reduced NPC1L1 expression in small intestine. Labonte et al revealed that NPC1L1 deficiency or
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Several CHK inhibitors have been reported in the
2019-09-09

Several CHK-1 inhibitors have been reported in the literature. Of these, UCN-01 (7-hydroxystaurosporine) is a potent inhibitor of CHK-1 (=5.6nM), , and has modest selectivity among other kinases. UCN-01 is currently in clinical trials. Other CHK-1 inhibitors reported in the literature include indaz
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In agreement with the evidence on the Plg
2019-09-09

In agreement with the evidence on the Plg-binding function of tapeworm enolases, eukaryotic enolases have been shown to be multifunctional proteins, with other activities besides their role as glycolytic enzymes (Pancholi, 2001). In this respect, several flatworms have been proved to express enolase
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(±)-Nutlin-3 and There are two types of DDRs DDR and DD
2019-09-09

There are two types of DDRs, DDR1 and DDR2, which are type I transmembrane RTKs characterized by an N-terminal extracellular discoidin domain containing a collagen binding site [8]. DDR1 expression is somewhat restricted to epithelial cells, while DDR2 is often expressed in cells of mesenchymal orig
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br Concluding remark br Acknowledgements br Detection and re
2019-09-09

Concluding remark Acknowledgements Detection and repair of the numerous, and potentially lethal, DNA lesions arising in human Carbidopa and daily is largely mediated by an efficient system collectively termed the DNA-damage response (DDR). Paradoxically, DNA-repair processes within cancer ce
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