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As small non coding RNAs microRNAs miRNAs can
2020-03-10

As small non-coding RNAs, microRNAs (miRNAs) can control gene expression at the post-transcriptional level by binding to the 3′-untranslated regions (3′-UTR) of messenger RNAs (mRNA) [15], [16]. miRNAs have been anticipated to regulate virtually all cellular mechanisms [17] and to play an important
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br Discussion Several DPP inhibitors are currently available
2020-03-10

Discussion Several DPP-4 inhibitors are currently available for use in the treatment of type 2 diabetes mellitus. Due to the different chemical structures there are marked differences both in the binding kinetics on the target enzyme [10] and also different pathways of elimination [13] exist. In
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193 2 synthesis Next we evaluated whether DPP inhibitor supp
2020-03-10

Next, we evaluated whether DPP-4 inhibitor suppressed osteoclast formation by downregulating LPS-induced RANKL expression in stromal cells; DPP-4 inhibitor did not inhibit LPS-induced RANKL expression. Furthermore, we evaluated the effect of DPP-4 on LPS-induced RANKL expression in stromal cells, bu
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Tumor cells exposed to the effect of
2020-03-10

Tumor CI 976 mg exposed to the effect of these compounds were shown to become chemo and radio-sensitive. Based on that, it was possible to anticipate the selectivity requirement for DNA-PK inhibition and the best route for their development. Accordingly, prompted by the clinical significance and th
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Our recent discovery M P H R A
2020-03-10

Our recent discovery (M.P., H.R., A.S.) of a highly selective and in vivo active DDR1 small-molecule inhibitor provides evidence that DDR1 is a druggable pharmaceutical target, and some details of our efforts are provided below. To avoid the repurposing of known kinase inhibitor structural motifs, w
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N fowleri enters the host through the nasal cavity
2020-03-10

N. fowleri enters the host through the nasal cavity and travels via the olfactory nerve into the Insulin (human) recombinant expressed in yeast mg where it causes PAM (Visvesvara and Stehr-Green, 1990). The ameba most commonly infects healthy young adults and children and is able to evade the immun
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Introduction Cysteinyl leukotrienes CysLTs LTC
2020-03-10

Introduction Cysteinyl leukotrienes (CysLTs), LTC4, LTD4 and LTE4, are 5-lipoxygenase pathway metabolites of arachidonic atr inhibitor and deeply involved in bronchial asthma via activation of CysLT1 receptors [1], [2]. Specific CysLT1 receptor antagonists, including pranlukast [3], [4] and montelu
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br Acknowledgements br Introduction Chemokines are a
2020-03-10

Acknowledgements Introduction Chemokines are a superfamily of chemotactic cytokines that play important roles in regulating cell migration and activation under inflammatory conditions (Nomiyama et al., 2008; Peatman and Liu, 2007; Zlotnik and Yoshie, 2000), such as angiogenesis (Arenberg et al
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br Material and methods br Results br Discussion
2020-03-10

Material and methods Results Discussion In vitro evidence indicates that LAS191859 is a potent CRTh2 antagonist as demonstrated in GTPγS binding studies with potency in the low nanomolar range and in addition it demonstrates a long receptor residence time. This potency is also maintained in
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Animal studies investigating the role of D dopamine
2020-03-10

Animal studies investigating the role of D1 dopamine receptors in the PFC have focused on delayed response tasks, which require online maintenance of a previously presented stimulus. Striatal dopamine is thought to be important for flexibility and updating goal representations when new information i
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It is of interest to point out that
2020-03-09

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 bun hot of fat, which was associated with a significantly reduced NPC1L1 expression in small intestine. Labonte et al revealed that NPC1L1 deficiency or e
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Fujimoto et al pointed out that RPN knockout
2020-03-09

Fujimoto et al. pointed out that RPN2 knockout alleviated the resistance of GC Aminoallyl-dUTP - Cy3 mg (MKN74 and KATO III) to docetaxel and DDP [23]. Yuan et al. demonstrated that the depletion of RPN2 resulted in the reduction in resistance of GC cells to drugs such as irinotecan, docetaxel, dox
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hiv fusion inhibitors In terms of its protease activity
2020-03-09

In terms of its protease activity, MME has a broad range of substrates being able to target glucagon, bradykinin, GLP1, and several other hiv fusion inhibitors of circulating small molecules [25]. MME has been shown to target free insulin B-chain [32], although whether MME could target and degrade
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br Cytokine impact on ILC fate
2020-03-09

Cytokine impact on ILC fate Increasing evidence shows that ILC2 and ILC3 may convert into ILC1-like Medroxyprogesterone acetate by downregulating either GATA3 or RORγt, respectively, upregulating T-bet and gaining the capacity for IFN-γ production [60,61]. This process, often referred to as ‘ILC
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br Acknowledgements br This work was
2020-03-09

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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