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Tenovin-6 synthesis br In vivo visualization of aromatase wi
2023-10-17
In vivo visualization of aromatase with positron emission tomography (PET) Positron emission tomography (PET) utilizes the high Tenovin-6 synthesis photons formed during the annihilation of positrons to detect the changes in the amount and localization of injected radiopharmaceuticals in the liv
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Weak and transient interactions of HMGB proteins
2023-10-16
Weak and transient interactions of HMGB proteins in such hit-and-run mechanisms are understandable given that “fluorescence loss in photobleaching” (FLIP) experiments employing GFP-labeled HMGBs have shown that in living cells they are the most mobile of all nuclear proteins [144]. The entire pool o
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For the derivatives a c another likely explanation for antif
2023-10-16
For the derivatives 3a–3c, another likely explanation for antifungal properties is that polymers bearing primary amine groups and secondary phosphoryl groups formed, enhancing complexation with the phosphate groups, and the complexes are amphiphilic (Palermo, Lee, Ramamoorthy, & Kuroda, 2011). The a
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At Johns Hopkins Aramco Health JHAH
2023-10-16
At Johns Hopkins Aramco Health (JHAH), we started an ASP in 2011 with an educational program of physicians and pharmacist. The program was enhanced mid-2012 with the following interventions: a re-designed antibiotic sensitivity report [2], intravenous to oral conversion program, vancomycin pharmacok
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The association of male gender with
2023-10-16
The association of male gender with increased atherosclerosis has stimulated interest in the role of androgen signalling in this condition. Androgens act (Fig. 2) by direct activation of androgen receptor (AR), a nuclear receptor that acts as a ligand-regulated transcription factor (Gao et al., 2005
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LOXs and CYPs are a series of iron containing
2023-10-16
LOXs and CYPs are a series of iron-containing enzymes that metabolize arachidonic glycoprotein iib iiia inhibitors to form biologically active products, such as epoxyeicosatrienoic acids (EETs) hydroperoxyeicosatetraenoic acids (HETEs), prostaglandins, leukotrienes and thromboxanes [6]. Among these
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Vanoxerine australia G has been shown to participate in
2023-10-16
Gβγ has been shown to participate in various MT-dependent processes such as cell growth and differentiation [15,[21], [22], [23], [24], [25], [26]]. G-protein β-subunit anti-sense oligonucleotides have been shown to inhibit cell proliferation and cause disorganization of the mitotic spindle in mamma
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Adenosine receptors are proposed to play proangiogenic role
2023-10-16
Adenosine receptors are proposed to play proangiogenic role in vascular and immune Esomeprazole Sodium australia within microenvironment of hypoxic tissues to maintain tissue oxygenation in chronic ischemic condition [9]. Adenosine also stimulates the production of angiopoetin-1, VEGF and Interleuk
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Owing to efficient catalytic character
2023-10-16
Owing to efficient catalytic character, high electrolyte accessible area, easy fabrication and many other interesting properties, metal oxide nanoparticles are extensively used in a variety of electro-analytical processes [14]. Metal oxide nanoparticles immobilized over a conductive and large area s
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We have previously shown that the antinociceptive effect of
2023-10-16
We have previously shown that the antinociceptive effect of tramadol, an analgesic that, like paracetamol is able to increase serotonin levels within CNS, is potentiated or antagonized respectively by a 5-HT1A/B nonspecific Mubritinib sale blockade or activation (Rojas-Corrales et al., 2000). Moreo
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SGI-1027 receptor Phospholipases cleave membrane phospholipi
2023-10-16
Phospholipases cleave membrane phospholipids from inflammatory cells, activated platelets, erythrocytes, adipocytes and cancer SGI-1027 receptor (Aoki et al., 2008, Neidlinger et al., 2006). Several reports have analysed the role of LPA and its receptors in the pathogenesis of RA. Zhao et al. repo
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Another topic for research will be
2023-10-16
Another topic for research will be the combination of other cytotoxic agents with Aurora kinase inhibitors. Particularly interesting might be the combination of Aurora kinase inhibitors and agents that depend on the spindle checkpoint for their activity, such as the taxanes, given the importance of
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exemplifies three of the compounds investigated in the selec
2023-10-16
exemplifies three of the compounds investigated in the selection for a candidate drug (CD). Our first criteria was an IC The SAR405838 receptor as such did not show any genotoxicity in the SOS/umu assay, but this does not say anything about any possible genotoxicity of its metabolites or degradati
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Many ruthenium complexes were tested
2023-10-16
Many ruthenium complexes were tested as potential anticancer agents and two complexes, namely NAMI-A (trans-[imH] [RuCl4(dmso-S)(im)]; im, imidazole) and KP1019 (trans-[indH][RuCl4(ind)2]; ind, indazole) have successfully entered clinical trials [27], [28]. NAMI-A is selectively active against metas
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br Methods and materials br Results br Discussion
2023-10-13
Methods and materials Results Discussion GPCR regulation in response to agonist stimulation is common to nearly all GPCRs and is essential in physiological systems to limit persistent signalling. In this study we have investigated the [Pyr1]apelin-13-induced trafficking and desensitization
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