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Phenolic compounds generated during biomass pretreatment
2021-02-07
Phenolic compounds generated during rhein pretreatment inhibit and/or deactivate cellulolytic/hemicellulolytic enzymes as well as the viability and fermentative capacity of yeast and bacteria [4], [5], [6], [7], [8], [9], [10], [11], [12], [13]. Phenolic compounds cause changes in protein conformat
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Besides EGFR other tyrosine kinase receptors are
2021-02-07
Besides EGFR, other tyrosine kinase receptors are currently gaining attention as potential therapeutic targets. Included among these is the fibroblast growth factor receptor (FGFR) family, which is involved in the progression of a variety of cancers.7, 8, 9, 10, 11 In lung cancer, fibroblast growth
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The potential off target activity of against
2021-02-07
The potential off-target activity of against other ATP-dependent enzymes, such as kinases, was also investigated. Encouragingly, there was no significant inhibition of ATP binding to 97 human kinases, when was evaluated at 10μM within a DiscoveRx scanEDGE® kinome screen (, ). All together, these dat
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br Discussion Electroporation is a convenient and
2021-02-07
Discussion Electroporation is a convenient and efficient way to introduce foreign material into octanoic acid [10], [16], [17], [18]. There are a lot of different protocols for transfection with electroporation. It was reported that there are several parameters that are relevant to successful el
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That DGAT mediated hepatic steatosis did not lead
2021-02-07
That DGAT-mediated hepatic steatosis did not lead to insulin resistance was clearly demonstrated in Liv-DGAT2-low mice by their normal blood glucose and plasma insulin levels, normal glucose and insulin tolerance, normal insulin sensitivity by hyperinsulinemic-euglycemic clamp studies, and normal he
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br Introduction br Sphingolipid metabolism Sphingolipids are
2021-02-07
Introduction Sphingolipid metabolism Sphingolipids, are fundamental constituents of all eukaryotic membranes and their metabolism is carried out by a broad array of anabolic and SCH727965 australia with ceramide as their hub (for a review, (Hannun and Obeid, 2018)). Ceramide can be formed by
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In this review focusing on
2021-02-07
In this review, focusing on biocatalyst “formate dehydrogenase FDH” catalyzing both of the formic Methoxyresorufin oxidation to CO2 and the CO2 reduction to formic acid, representative examples of properties, types, structure of active-site of FDH and, reaction mechanism of formic acid oxidation an
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Pharmacogenomics is the study of the role of the genome
2021-02-07
Pharmacogenomics is the study of the role of the Lopinavir in drug response. It was reported that the effectiveness of atorvastatin was affected by genetic factors.26, 27 In previous studies, there are many genetic polymorphisms related to the efficacy of atorvastatin. Cerda et al reported that SCA
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First we synthesized inhibitor following the patent procedur
2021-02-05
First, we synthesized inhibitor following the patent procedure reported by Shewchuk et al. to provide its first complete characterization (see ). Two different synthetic approaches were used to obtain compounds –. The first method relied on the alkylation of the common 5-phenol-2,4-diaminopyrimidin
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This letter reports an ab
2021-02-05
This letter reports an ab initio study on the X peaks of PES by including the SO effect. The multiplet split energies are calculated with the SO-MCQDPT2 method [21], and the so-called pole strengths are evaluated to simulate the relative intensities. The results are compared with the experimental PE
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Recent studies show that the
2021-02-05
Recent studies show that the expression and function of some ion channels such as voltage-gated potassium channels, sodium channels and calcium channels are closely related to the proliferation, migration, and invasion of tumor cells [40], [41], [42]. Firstly, the expression of ion channels is chang
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For this reason downstream components
2021-02-05
For this reason, downstream components of the inflammatory pathway have been investigated in the search for alternative targets. Targeting such downstream elements might result in safer and more tolerable analgesics. PGE mediates its effects through binding to four G-protein-coupled receptors (EP1-4
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br Results br Discussion The
2021-02-05
Results Discussion The process by which MBCs differentiate from GC B cell precursors remains mostly uncharacterized, in large part because of the uncertainty surrounding the nature of the precursor N-acetyl D-galactosamine within the GC. The identification here of a distinct subset of GC B ce
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An important role for the precursor molecule of
2021-02-05
An important role for the precursor molecule of the main EBI2 ligand, 25-OHC, in the inhibition of inflammation was recently shown. 25-OHC was demonstrated to inhibit inflammasome induction in mouse macrophages [28]. Inflammasome assemblies are the sites of caspase 1 activation and lead to the gener
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mecamylamine This hydrophobic biphenyl tail gave good bindin
2021-02-04
This hydrophobic biphenyl tail gave good binding affinity for human DHODH enzyme (IC mecamylamine was found to be the main metabolite in human microsomes and it was 100-fold less active against hDHODH than the ester. In an attempt to identify the specific non-covalent binding interactions which we
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