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substance p Acanthopanax senticosus Rupr Maxim Harms a nonto
2021-03-29

Acanthopanax senticosus (Rupr. & Maxim.) Harms, a nontoxic herb belongs to the family of Araliaceae, which found in Northeast Asia. A. senticosus traditionally used as a tonic to treat rheumatism, diabetes, and hepatitis [7]. Previous phytochemical and biological investigations found its roots and s
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Global inhibition of integrin signaling with EDTA
2021-03-29

Global inhibition of integrin signaling with EDTA here suggests that integrin signaling potentially cooperates with DDR2 in collagen induction of lysyl oxidase. This notion is supported by a recent study that shows DDR2 cooperation with specific integrins in cell adhesion to collagen [47]. It is of
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Confirmation of the presence of
2021-03-29

Confirmation of the presence of H+-PPase genes in the genomes of the different protists tested was obtained by Southern blot analyses using the PCR-amplified DNA fragments as probes (Fig. 3). In the trypanosomatids L. major and T. cruzi and the euglenoid A. longa, a single band appeared in the filte
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br Limitations There are some limitations to take into
2021-03-29

Limitations There are some limitations to take into account when interpreting these results. Firstly, direct causation cannot be established in this cross-sectional study, and it may be the downstream effects of TNFα, such as increased 172 5 production, which are more proximally related to cogni
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Pyrazolopyrimidines are bioisostere of purine exhibit promis
2021-03-29

Pyrazolopyrimidines are bioisostere of purine exhibit promising antitumor activity by competitively binding to the ATP active site of different kinase Mifepristone [16,17]. Several compounds of this family were found to induce apoptosis and/or reduce cell proliferation in various solid tumour and l
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A phenylacetic acid derivative discovered in a high throughp
2021-03-29

A phenylacetic CGP 53353 synthesis derivative (), discovered in a high throughput screen for CRTH2, inhibited the binding of H-PGD to CRTH2 receptors on 293 cells with an IC of 0.010μM, and inhibited the binding of H-PGD to DP receptors with an IC of only 8.3μM (). Compound also inhibited CRTH2 m
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br Experimental section br Results
2021-03-29

Experimental section Results Discussion In our previous work (Rashidi et al., 2018) we isolated a novel glucarpidase whose raised dcp cas synthesis did not cross-react with the one in clinical use. In principle, therefore, it would be possible to delay the production of antibodies in a pati
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The regression also revealed a
2021-03-29

The regression also revealed a significant association between admission selectivity (SELECT) and exam pass rate (PASS%) (p arginase inhibitors serve as an indicator of a student’s ability to learn and their aptitude for academic success. These same qualities likely enable more selective schools to
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Although the presence of at least one
2021-03-29

Although the presence of at least one triple helix domain is typically the collagen signature, collagens are modular proteins composed of a succession of collagenous (COL) and non-collagenous domains (NC) that are both involved in collagen functions and in receptor binding. COL domains are linked by
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More recently it was discovered that BChE hydrolyzes the neu
2021-03-29

More recently, it was discovered that BChE hydrolyzes the neuropeptide gut hormone, ghrelin [25], [26], [27], [28]. Nonetheless, because the enzyme reaction is very slow, those who first reported this finding were initially reluctant to attribute a real physiological role for that phenomenon. Our ow
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In mouse lung arsenite enhances
2021-03-29

In mouse lung, arsenite enhances the formation of cigarette smoke-induced 8-oxodeoxyguanine (Hays et al., 2006) and BaP-induced DNA adducts (Evans et al., 2004). Moreover, arsenite inhibits the repair of BaP-induced DNA adducts in human lung carcinoma A549 SB-222200 (Schwerdtle et al., 2003), indic
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The underlying mechanisms of how progesterone prolongs pregn
2021-03-29

The underlying mechanisms of how progesterone prolongs pregnancy, although not completely understood, are thought to have to do with reduction in uterine contractility, antimicrobial protein up-regulation, immunosuppression, and inflammatory inhibition. Specific to preterm PROM, progesterone has bee
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br Materials and methods br
2021-03-29

Materials and methods Results Discussion A reporter of FGF signaling activity has long been sought to facilitate the quantitative real-time analysis of pathway activity at single-cell resolution. Here we report the generation of a Spry4 reporter allele in ESCs and mice that recapitulates kn
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br Experiments br Numerical simulations br Discussion br Con
2021-03-29

Experiments Numerical simulations Discussion Conclusions By large-caliber PELE with various d/D against RHA plate at low velocity of 415 m s−1, impact experiments against 30 mm RHA target were carried out. Numerical simulations were also conducted to monitor progress of PELE expansion an
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Among RAS mutant tumors analyzed we found that the efficacy
2021-03-29

Among RAS mutant tumors analyzed, we found that the efficacy of either the SHP2 inhibitor SHP099, or combined MEK and SHP2 inhibition was best in those expressing RAS mutations at G12 (Figure 7B). Recent studies revealed that cellular RAS(G12C) activity depends on RTK-mediated nucleotide exchange, a
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