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Unexpectedly under pathological pain conditions inhibition o
2025-01-06

Unexpectedly, under pathological pain conditions, inhibition of spinal glutamate transporter activity can produce antinociceptive effects. For example, intrathecal injection of the transportable inhibitor trans-pyrrolidine-2,4-dicarboxylic cAMPS-Rp, triethylammonium salt mg (t-PDC) or antisense oli
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Plant material and growth conditions Arabidopsis thaliana ec
2025-01-04

Plant material and growth conditions. Arabidopsis thaliana ecotype Columbia was grown on a mixture of soil, vermiculite, and perlite (4:2:1) with a 16h light/8h dark Cathepsin K Activity Fluorometric Assay Kit in a temperature-controlled growth room (22°C), unless indicated otherwise. Molecular c
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br Free entry equilibrium At
2025-01-04

Free entry equilibrium At stage 2 of the game, n ≥ 2 firms simultaneously decide whether or not to enter the industry. Market entry involves a sunk fixed cost f > 0, which we assume cannot be subtracted from the tax base. Our assumption reflects that deductions of market entry costs are often inc
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The first natural product described as LO
2025-01-04

The first natural product described as 5-LO inhibitor was the polyphenol nordihydroguaiaretic Plant growth regulator 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 befo
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sesamin In an AP scenario several inflammatory
2025-01-04

In an AP scenario, several inflammatory mediators are produced locally to orchestrate an immune response. Eicosanoids are among those molecules and represent a class of lipid mediators synthesized from arachidonic sesamin through the action of cyclooxygenases or lipoxygenases to generate prostaglan
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br Acknowledgements br Introduction Thus damage to the nervo
2025-01-04

Acknowledgements Introduction Thus, damage to the Carcinoid syndrome therapy may produce severe consequences (National Research Council, 1992). Indeed, though the nervous system has several compensatory and adaptive mechanisms, it is vulnerable to toxic insult, due to its inability to regener
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Evidences have suggested that impairment of CK
2025-01-04

Evidences have suggested that impairment of CK activity contributes to inhibition of Na+, K+-ATPase and H+-ATPase activities during infectious diseases, since these ATPases are dependent of ATP, as observed by Baldissera et al. [31] in fish experimentally infected by Aeromonas caviae. We observed th
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br Model Fig demonstrates the block
2025-01-04

Model Fig. 1 demonstrates the block-scheme of main interactions between variables of the model under investigation. These interactions are described below in details and are expressed in mathematical form as well, where all variables are the functions of space and time coordinates, r and t, which
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br Conclusion These studies broadly demonstrate that dopamin
2025-01-03

Conclusion These studies broadly demonstrate that dopamine and endocannabinoid signaling in the NAc can have diverse effects on AMPAR-mediated synaptic function depending on previous psychostimulant experience. Here, we examined mechanisms underlying the depotentiation of AMPAR-mediated synaptic
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br Results br Discussion Using primarily an electrophysiolog
2025-01-03

Results Discussion Using primarily an electrophysiological analysis of dysbindin-deficient hippocampal neurons in cultures and slices, we have uncovered a previously unreported role for dysbindin in enhancing CA3–CA1 AMPAR-mediated transmission. An earlier study, however, has reported a reduct
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Physcion Salvia the largest genus in the family Lamiaceae
2025-01-03

Salvia, the largest genus in the family Lamiaceae, comprises over 900 species that are distributed globally [14], [15], [16]. The genus Salvia has been assessed in many studies because it is a rich source of polyphenol compounds, of which more than 160 have been isolated from plants in the genus, so
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br Conclusions br Introduction During numerous
2025-01-03

Conclusions Introduction During numerous physiological processes, aldehydes are generated from a variety of endogenous and exogenous precursors including amino acids, carbohydrates, and lipids [1]. Most aldehydes are highly reactive and cytotoxic due to the strong electrophilic nature of the t
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A high throughput small molecule
2025-01-03

A high-throughput small molecule ACK1 biochemical inhibition screen was performed in-house and led to the identification of 1μM inhibitor furanopyrimidine (). Further binding studies found Nitecapone to be both ATP-competitive and reversible. Early structure-activity relationship (SAR) work was perf
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nalidixic acid The present in vitro pharmacological experime
2025-01-03

The present in vitro pharmacological experiments revealed that the cholinergic up-regulation of VEGF expression in neurons and astrocytes was mainly mediated by nicotinic AChR and muscarinic AChR, respectively. In addition, neuronal VEGF expression was elevated by endogenous ACh in a manner that was
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br Acknowledgments This work was supported by a grant
2025-01-03

Acknowledgments This work was supported by a grant of the Romanian National Authority for Scientific Research, CNCS – UEFISCDI, project no. PN-II-ID-PCE-2011-3-0571, awarded to F.A.M. D.V.N. was co-financed from the European Social Fund through Sectorial Operational Program Human Resources Develo
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