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br Acknowledgements The present work was funded by National
2020-07-30

Acknowledgements The present work was funded by National Natural Science Foundation of China (No. 816712276 and No. 81771147), Natural Science Foundation of Shandong Province (ZR2016HM30), Medical and Health Development Program of Shandong Province (2016WSB33025), 2015 Science and Technology Deve
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Classical DHFR inhibitors such as methotrexate MTX bind tigh
2020-07-29

Classical DHFR inhibitors such as methotrexate (MTX) bind tightly to the enzyme and possess adequate clinical pharmacokinetics. MTX bind to the DHFR binding site through the formation of hydrogen bonds with Asn64, Lys68, Arg28, Arg70, Val115 and Ile7 amino tranylcypromine residues as well as hydrop
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In conclusion MEN behave as
2020-07-29

In conclusion, MEN91507 behave as a potent and selective CysLT1antagonist in guinea-pigs and human in vitro assays. In vivo, MEN91507 shares with the other CysLT1 antagonists anti-bronchospastic and anti-inflammatory effects; since these effects are long-lasting and are also observed following the o
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2 deoxy d glucose In the present study we isolated a
2020-07-29

In the present study, we isolated a full-length GluCl cDNA (named as CsGluCl) from C. suppressalis. We report the expression patterns of three CsGluCl variants and document the role of CsGluCl in abamectin toxicity and C. suppressalis development. Our results are pivotal to the discovery of new chem
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The roles of ginsenoside in
2020-07-28

The roles of ginsenoside in E1 and 26S proteasome inhibition are shown in Table 2. The nitro substitute on the furan ring may be important for PYR-41 inhibition of the E1 enzyme (Yang et al., 2007). The macrocycle core and aliphatic tail of Largazole are responsible for inhibiting E1 activity (Unge
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The CysLT receptor is highly expressed
2020-07-28

The CysLT1 receptor is highly expressed in the lung, which may be relevant for its implication in pulmonary diseases like asthma. In fact, specific antagonists of the CysLT1 receptor (pranlukast, montelukast and zafirlukast) are used in the clinic to control bronchoconstriction and inflammation in a
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Few studies have been reported on the selectivity of prolyl
2020-07-28

Few studies have been reported on the selectivity of prolyl hydroxylase inhibitors for different types of prolyl hydroxylases, including for the PHD inhibitors in clinical trials.3, 16 This is important, especially for applications in the treatment of chronic diseases, e.g. anaemia.1, 2, 3 A recent
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The zymography procedure using salmon PG has been
2020-07-27

The zymography procedure using salmon PG has been described in the Supplemental Information. CHase ABC and BTH, which are sodium dodecyl sulfate (SDS)-resistant enzymes, were clearly detected in the PG-substrate SDS polyacrylamide gel at each predicted size by staining with Alcian Blue (). The minim
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br Funding source s This work was supported
2020-07-27

Funding source(s) This work was supported by NIH MH107648 to E.G. Conflicts of interest Introduction Maternal behavior in rats involves dramatic changes in the perceptional, emotional and motivational responses of female rats towards infant rats (Numan and Young, 2016). Through mother-infa
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Zoniporide dihydrochloride mg Many organochlorine insecticid
2020-07-27

Many organochlorine insecticides, including MXC, are used in agriculture [1,2]. Thus, these compounds contribute to a health risk not only to agricultural workers but also to the general population. Here we identify additional mechanisms of HPTE in regulating neurosteroid formation and reinforce pre
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DDR receptor effector mechanisms are not
2020-07-27

DDR receptor effector mechanisms are not well understood. Most descriptions of DDR function have focused on downstream signaling pathways activated by collagen that regulate cell proliferation and transcriptional activation [7]. Natural occurring or induced DDR2−/− genotypes in mice induce dwarfism,
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The cardiotoxicity of NSAIDs except for aspirin are
2020-07-27

The cardiotoxicity of NSAIDs, except for aspirin, are well reported in many studies, and the food and drug administration (FDA) of the USA warned about the cardiovascular toxicities of NSAIDs [6]. NSAID treatment is associated with elevated blood pressure, stroke, and myocardial infarction [6,7]. Al
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Unlike CRM exportins Cse and Xpot
2020-07-27

Unlike CRM1, exportins Cse1 and Xpot lack a C-extension and instead rely primarily on changes in HEAT-repeat conformation and direct Ran-cargo contacts to ensure low cargo-binding affinity in the cytosol and cooperative assembly of the exportin/Ran/cargo complex in the nucleus (Cook et al., 2005, Co
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For CRM substrate binding to occur
2020-07-27

For CRM1-substrate binding to occur, the cargo molecule must have a leucine-rich NES (Wen et al., 1995, Fukuda et al., 1997). The NES for CRM1 contains hydrophobic amino acids, including isoleucine, leucine, methionine, phenylalanine, and valine (Kutay & Guttinger, 2005). A consensus motif for this
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br Introduction br Materials and methods br Results
2020-07-27

Introduction Materials and methods Results Discussion In the present study, etifoxine attenuated the anxiogenic-like behavioral and autonomic responses to i.c.v. injection of CRF in the rodent. Thus, in the open field, rats receiving CRF responded with an increased sensitivity to the str
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