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Polycyclic aromatic hydrocarbons PAHs are abundant environme
2024-07-16
Polycyclic aromatic hydrocarbons (PAHs) are abundant environmental contaminants that are produced by the incomplete combustion of organic matter, combustion engines, residential heating, SB 290157 trifluoroacetate salt synthesis burning, and industrial activities (Gelboin, 1980; Phillips, 1999, Phil
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PAN induced nephrosis was accompanied
2024-07-16
PAN-induced nephrosis was accompanied by loss of body weight, decrease of food intake, increase in urine volume and increases in triglycerides and cholesterol levels, which have been reported previously (Natori et al., 1996). Except for urine volume, each one of these measures was improved by A-3069
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In this study we obtained the absorbance and photoluminescen
2024-07-16
In this study, we obtained the absorbance and photoluminescence (PL) of Exo1 polymerized with various types of actin-binding proteins in order to probe the actin structures in situ without labeling. Both optical measurements have been useful in examining biomaterials such as DNA and proteins withou
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Most studies on d penicillamine induced
2024-07-16
Most studies on d-penicillamine-induced MG were performed before the discovery that some MG patients have anti-MuSK antibodies. After the identification of the present case, we retrospectively tested the stored frozen sera of ten earlier identified d-penicillamine MG patients with anti-AChR src inhi
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proton pump inhibitor br Conclusion Biotransformation of tra
2024-07-16
Conclusion Biotransformation of trachyloban-19-oic proton pump inhibitor by S. racemosum provided three products. Oxidation of compound 1 at C-17 (2–3), as well as rearrangement of 1 into a kaurane diterpene hydroxylated in C-16 and C-17 (4) were crucial for increasing AChE inhibitory activity.
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PNU 37883 hydrochloride br Materials and methods br Results
2024-07-16
Materials and methods Results The determination of the intrinsic inhibitory potential of the oximes HI-6 and MMB-4 with human and guinea pig AChE revealed marked differences between both oximes (Table 1). MMB-4 had an only marginal effect on both AChE species, calculated IC50 of >1000μM, while
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Bioactive peptides contain amino acids
2024-07-16
Bioactive peptides contain 2–20 amino acids with possible bioactivities including antihypertensive, antioxidant, antimicrobial, anticancer, and opioid activity [9], [10], [11]. There has been a great interest in antihypertensive peptides for their efficiency in lowering blood pressure. The antihyper
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The first natural product described
2024-07-16
The first natural product described as 5-LO inhibitor was the polyphenol nordihydroguaiaretic L-703,664 succinate from the Mexican dessert plant Larrea divaricata in 1981 (Bokoch and Reed, 1981), short after the initial identification of 5-LO in 1979 (Borgeat and Samuelsson, 1979). Long time before
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The srd a isoforms showed
2024-07-16
The srd5a isoforms showed unique expression profiles in early FHM development (Fig. 2). Similar to amphibian embryos, there was a high abundance of both srd5a1 and srd5a3 at 1dpf in FHMs, suggesting that mRNA for these enzymes may be maternally deposited and that these enzymes may play a key role in
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Introduction Lysophosphatidic acid LPA is a key serum borne
2024-07-16
Introduction Lysophosphatidic 3 poly a tail (LPA) is a key, serum-borne phospholipid, regulating a number of cellular processes such as proliferation, migration and differentiation through its interaction with G-protein coupled receptors. LPA receptor signaling has been implicated in several disea
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Compound was docked into the active site
2024-07-16
Compound was docked into the active site of Aurora B kinase using Tripos sybyl-X ver. 2.1.1. The crystal structure of human Aurora B kinase cocrystallized with its potent inhibitor VX-680 was used for the docking analysis (PDB ID: ). The most likely binding conformations were selected based on the
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br Experimental procedures br Results br Discussion Although
2024-07-16
Experimental procedures Results Discussion Although previous studies have indicated that astrocyte aromatase plays a role in nociceptive processes (O'Brien et al., 2015, Smeester et al., 2016), the mechanisms responsible for the regulation of aromatase and its involvement in nociception rem
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br Conclusions In the current study we found that
2024-07-16
Conclusions In the current study, we found that the exposure of maduramicin to chicken myocardial GDC-0084 results in cellular damage and even death via the induction of apoptosis. Maduramicin upregulated the expression of apoptotic genes and activated caspase cascades, which were accompanied by
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br Acknowledgments This work was
2024-07-15
Acknowledgments This work was supported by grants from the “Agence Nationale de la Recherche” ANR-09-CESA-006 program, the Agence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du Travail (Anses, Project n° 2012-2-077) and the Interdisciplinary Program “Longévité et Viei
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Dose Response Studies Against Puromycin
2024-07-15
Dose–Response Studies Against Puromycin–Sensitive Aminopeptidase (PSA). PSA is a ubiquitous metallopeptidase encoded by the NPEPPS gene with subcellular distribution in the cytosol and nucleus [49]. Comprising of a 919 amino Apoptosis Inhibitor sequence, it has a broad substrate specificity, and is
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