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Materials and methods Cell culture and receptor
2019-07-15
Materials and methods Cell culture and receptor gene transfection. PC12 BMS 777607 were purchased from the Institute of Cell Biology, Chinese Academy of Sciences, Shanghai, China. The cDNA for mouse CysLT1 or CysLT2 receptor (mCysLT1 and mCysLT2, subcloned into pcDNA3.0) was kindly gifted by Profe
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Several highly potent CysLT receptor antagonists with large
2019-07-15
Several highly potent CysLT1 receptor antagonists with large structural Valproic acid sodium salt where have been developed. Beyond antagonists with structures analogous to cysteinyl leukotrienes, other subclasses comprise: (a) hydroxyacetophenones, (b) indoles and indazoles, (c) quinolines, benzot
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Ramos cell http www apexbt com media
2019-07-15
Ramos cells carry a non-functional p53 and constitutively express the transcription factor, NF-κB (Nazari et al., 2011, Zand et al., 2008). There is much evidence to support the conclusion that the interruption of NF-κB activation promotes apoptosis in several hematological malignancies (Fabre et al
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Dipraglurant Interest in the PGE EP pathway is increasing gi
2019-07-15
Interest in the PGE2/EP4 pathway is increasing given its diverse capability of regulating central nervous system activity [13]. EP4 has a protective function by reducing cerebral injury and improving functional outcome after stroke [14], and in suppressing Dipraglurant inflammation [15]. The EP4 re
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br Acknowledgements br Introduction Endothelial cells consti
2019-07-15
Acknowledgements Introduction Endothelial IRAK inhibitor 1 constitute a unique source of humoral factors that may regulate the functions of other cell types via paracrine or endocrine pathways [1]. Among the many molecules originated from the endothelium, nitric oxide (NO) plays versatile rol
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The discovery of proteases that are active in organic solven
2019-07-15
The discovery of proteases that are active in organic solvent media has greatly extended their ability in the synthesis of useful products. Microbial proteases which are able be catalyse in non-aqueous solvents present new expectation in enzyme applications. This kind of enzymes gives a major contri
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In the present study we used linagliptin one of
2019-07-15
In the present study, we used linagliptin, one of the commercially available DPP-4 inhibitors, because it has more long-lasting inhibition of DPP-4 activity than other drugs of this class. We hypothesized that linagliptin may interact with intercellular components, not only with DPP-4 on the plasma
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HA activates its receptor channels to cause an
2019-07-13
HA activates its receptor channels to cause an inward chloride flux in the insect nervous system (Hardie, 1989).
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For reductive amination by L AmDH the term related to
2019-07-12
For reductive amination by L-AmDH, the term related to the enzyme-ammonia complex is excluded rather than the enzyme-pentanone term (Table 1).
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Finally this study described that the lead compound acted
2019-07-11
Finally, this study described that the lead CEP-32496 (1) acted as an efficient alkylating agent for the G4 structure in addition to the previously reported T-T mismatch structure.
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Zoledronic Acid The contribution of Interference
2019-07-10
The contribution of Interference RNA and epigenetic in OA attenuation Interference RNA, a cellular mechanism for post-transcriptional gene silencing that is associated with mRNA.
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Adding more pieces to the puzzle using a
2019-07-09
Adding more pieces to the puzzle, using a human-to-animal crossover study, blood taken from healthy volunteers that underwent exercise was used as a dialysate to perfuse a rabbit heart in a Langendorff model of MI [62].
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The crystal structure of full length CHK is still
2019-07-08
The crystal structure of full-length CHK is still unsolved. However, the close homology between CHK and Csk suggests that these kinases share a similar structure.
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Materials and methods Results
2019-07-05
Materials and methods Results Discussion We initially found that ISL, a natural product with a linear scaffold (2-propenone), is able to inhibit CK2 (IC50 = 17.3 μM). Then we have investigated the inhibitory potential of a novel series of compounds with linear scaffolds by combining fragment-hybrid computational design with in vitro assays.
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As described above when EGCG was orally administered
2019-07-04
As described above, when EGCG was orally administered, CYP3A expression in the liver decreased; however, the CYP3A expression level in the intestine was unchanged (Fig. 3).
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