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AP and NF B activation is inhibited by
2022-05-25

AP-1 [16], [17] and NF-κB activation is inhibited by curcumin (diferuloylmethane) [18], [19], the yellow component of Curcuma longa that gives curry its colour and flavour. Curcumin has shown anti-inflammatory and antioxidant properties [20], [21], [22], [23], [24], [25], [26] due to the inhibition
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Nitrosylation mediated post translational modifications of p
2022-05-25

Nitrosylation-mediated post-translational modifications of proteins through GSNOR play critical roles in modulating plant defense responses to diverse abiotic and biotic stresses (Frungillo et al., 2013, Leterrier 2011). As the most fundamental and intricate physiological process of plants, photosyn
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Decreasing GSK activity has therapeutic benefits in
2022-05-25

Decreasing GSK-3β activity has therapeutic benefits in animal model of colitis [45] and traumatic bromhexine receptor injury [46] and ischemia/reperfusion injury [47,48]. In brain, activation of GSK-3β promotes Aβ toxicity by elevating APP expression and its amyloidogenic cleavage, and by dysregula
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br Introduction Human immunodeficiency virus HIV is a retrov
2022-05-25

Introduction Human immunodeficiency virus-1 (HIV-1) is a retrovirus that primarily infects components of the human immune system, such as CD4+ T cells, macrophages and dendritic Phos-tag (Clapham and McKnight, 2001). HIV directly and indirectly destroys CD4+ T cells, which leads to severe immunod
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In the present study we aimed to investigate the
2022-05-25

In the present study, we aimed to investigate the effect of a common dairy and beef genetic background on the mRNA GFP Quantitation Kit of the AdipoQ system and GPR109A in different adipose depots and liver. Materials and Methods Results Comparing fat masses between families (fat-type vs. le
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Currently ursodeoxycholic acid UDCA is the only recommended
2022-05-25

Currently, ursodeoxycholic Autophagy Compound Library (UDCA) is the only recommended and widely used drug in the treatment of CFLD. However, the clinical efficacy of UDCA is controversial. The most recent Cochrane review only identified a small number of trials assessing the effectiveness of UDCA [9
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br Conflict of interest br
2022-05-25

Conflict of interest CRediT authorship contribution statement Magdalena Olga Ciechanowska: Conceptualization, Data curation, Investigation, Methodology, Project administration, Writing - original draft. Magdalena Łapot: Formal analysis, Investigation, Methodology. Marek Kowalczyk: Writing - re
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Previous studies have shown that
2022-05-25

Previous studies have shown that zinc interacts with other allosteric modulators at the glycine receptor (Kirson et al., 2013, McCracken et al., 2010, McCracken et al., 2013). Of note, the chelation of zinc via tricine decreases the effects of alcohol at α1-, α2-, and α3-containing glycine receptors
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The ion conduction pathway reported herein accounts for all
2022-05-25

The ion conduction pathway reported herein accounts for all known functional properties of EAAT/GltPh anion channels. Simulations reveal unitary current amplitudes and ion selectivities (Figures 3C and 3D) that resemble experimental results (Melzer et al., 2003, Wadiche and Kavanaugh, 1998). The cal
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In conclusion atorvastatin but not
2022-05-25

In conclusion, atorvastatin but not pravastatin impaired glucose utilization in C2C12 cells and glucose tolerance in HFD mice, which may be partly due to the inhibition of GLUT4 translocation in muscle cells. The decrease in the cholesterol level induced by atorvastatin may partly account for the in
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The energy required to drive the functional process to activ
2022-05-25

The energy required to drive the functional process to actively maintain lens transparency is primarily derived from the metabolism of glucose. Since the lens is avascular and exists in an environment of low oxygen tension, glucose is primarily metabolized by Ranolazine 2HCl glycolysis (Kinoshita, 1
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br Acknowledgments We would like to acknowledge Jenna
2022-05-25

Acknowledgments We would like to acknowledge Jenna Hall, Marita Rivir, Kathleen Smith, Joyce Sorrell, and Emily Yates for assistance with in vivo pharmacology studies. We would like to acknowledge Joe Chabenne and Steph Mowery for assistance with in vitro cell-based assays, and Patrick J. Knerr f
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br Structures of human secretase Before
2022-05-25

Structures of human γ-secretase Before the near-atomic resolution structures, the highest resolutions achieved for γ-secretase were 15 and 12Å [19, 21]. The 15-Å structure revealed a MOG (35-55) chamber in the transmembrane domain and two pores at the top and bottom of γ-secretase, which were spe
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The current gold standard for diagnosing BAM or
2022-05-24

The current gold standard for diagnosing BAM or BAD is the measurement of BA turnover rate with radiolabelled tauroselcholic (75selenium) NAD/NADH Quantitation Colorimetric Kit synthesis (also known as the SeHCAT retention test). SeHCAT test involves the use of a synthetic analogue of naturally occ
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The co crystal structure of GPR complexed with TAK provided
2022-05-24

The co-crystal structure of GPR40 complexed with TAK-875 provided precise structural information for the rational design of novel GPR40 agonists. The key interactions between the carboxylate with the residues Arg183, Arg258, Tyr91 and Tyr240 of GPR40 were observed. And Trp174ECL2 was oriented nearly
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