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The present study provides the first
2021-07-15
The present study provides the first evidence that the human uroepithelial R547 in vitro respond directly, within 48h, to this carcinogen by promoting extensive vacuolation and DAPK expression. By using the TEM, ICC and Western blotting, we found that the arsenite-induced vacuoles were derived from
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Substitutions on the benzene ring of the phenyl acetic acid
2021-07-14
Substitutions on the benzene ring of the phenyl acetic pd 1 receptor moiety were evaluated to study their effect on DP and CRTH2 selectivity (). Compound has strong affinity for CRTH2, but it only has moderate affinity for DP. Small substitutions such as methoxy () and fluorine () next to the arylox
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br Conclusion The preclinical data reported in this study
2021-07-14
Conclusion The preclinical data reported in this study shows that LAS191859 is a potent and safe CRTh2 antagonist, with a long receptor residence time that provides a sustained in vivo efficacy. This property is reflected in the prolonged duration of action of LAS191859 in in vitro and in vivo fu
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There have been attempts to stimulate the
2021-07-14
There have been attempts to stimulate the dopaminergic system to influence cognition in women around menopause who have subjective complaints about their cognition by Epperson et al. (Epperson et al., 2011, Epperson et al., 2015). In perimenopausal and postmenopausal women, Epperson et al. found tha
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protease activated receptor In this context our observation
2021-07-14
In this context, our observation that the protease activated receptor predictor of positive QFN-CMV responses is background CMV seropositivity was not unexpected. Older age, despite well-known effects of CMV memory inflation did not appear to independently impact QFN-CMV responses in our study. The
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Alzheimer s disease AD is a chronic progressive neurodegener
2021-07-14
Alzheimer’s disease (AD) is a chronic, progressive neurodegenerative disorder of the inos inhibitor which is considered a leading cause of dementia and affects 20–30 million people worldwide. Presently, a suitable treatment and prevention strategy against AD is hardly available. Various studies hav
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br Acknowledgements This work was supported in
2021-07-14
Acknowledgements This work was supported in part by JSPS KAKENHI Grant Number 26292031. Introduction The Cys-loop receptors constitute an important superfamily of ligand-gated ion dexamethasone acetate receptor (LGICs) and mediate synaptic transmission in both invertebrate and vertebrate ner
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ERK and p MAPK signaling pathways play critical
2021-07-14
ERK and p38 MAPK signaling pathways play critical role in genesis and metastasis of melanoma (Tang et al., 2018). >50% of melanoma Narciclasine receptor (Abildgaard and Guldberg, 2015) show abnormal activity of BRAF-RAS-RAF to activate MEK signal that drives the growth-promoting extracellular signa
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MAPKs are a family of phosphorylating enzymes that orchestra
2021-07-14
MAPKs are a family of phosphorylating enzymes that orchestrate various cellular response in proliferation, apoptosis, inflammation, stress response, and energy metabolism [11]. There are at least four major members including extracellular signal-regulated kinase 1 and 2 (ERK1/2), p38 mitogen-activat
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ACE also known as Kininase II
2021-07-14
ACE also known as Kininase II is an important enzyme of the Renin angiotensin Paroxetine HCl mg system (RAAS) (Novo et al., 1987), it is believed to be a potent blood pressure regulator and also plays a crucial role in activation of the bradykinin receptor via inactivation of bradykinin which works
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br Conclusions br ISG is an
2021-07-14
Conclusions ISG15 is an ubiquitin‐like protein that is induced by treating mammalian Thalidomide with interferon‐α/β. UbE1L was identified as the E1‐activating enzyme for ISG15 in the course of experiments that demonstrated that the nonstructural or NS1 protein of influenza B virus inhibits IS
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br Conclusions Overexpression of DDR
2021-07-13
Conclusions Overexpression of DDR2 might contribute to tumor progression in lung SQCC, and the T681I mutation we found in this work is an inactivating mutation. There is a possibility that not only activating mutation but also overexpression of DDR2 might be a molecular target for treatment of lu
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Collectively the results presented here provide new insights
2021-07-13
Collectively, the results presented here provide new insights into ligand binding, clustering, spatial distribution, and phosphorylation of DDR1b and DDR2 in response to soluble collagen I. As depicted in the cartoon of Scheme 1, we postulate a model in which the spatial distribution and assembly of
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Harringtonine An important strength of our
2021-07-13
An important strength of our study is the use of an elastic net regression model to select the variable and construct the model, which performed ideally in terms of both predictive accuracy and sparsity for the high-dimensional datasets [16]. As a result, the apparent predictive effect of multiple c
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We next considered the mechanism of the hepatospecific decre
2021-07-13
We next considered the mechanism of the hepatospecific decrease in CYP3A exerted by EGCG. We examined the possibility that orally administered EGCG was absorbed from the intestine and directly decreased the CYP3A expression level in the liver. Although the 6-Aminonicotinamide synthesis rate of orall
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