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br Materials and methods br Results br Discussion
2020-02-19

Materials and methods Results Discussion We initially found that ISL, a natural product with a linear scaffold (2-propenone), is able to inhibit CK2 (IC50 = 17.3 μM). Then we have investigated the inhibitory potential of a novel series of compounds with linear scaffolds by combining fragmen
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For the current studies we used the selective Epac
2020-02-19

For the current studies, we used the selective Epac agonist 8CPT-AM to directly activate the proteins. We chose this pharmacological approach since it allows a direct activation of Epacs rather than using receptor agonists such as PGE2 which could introduce confounding variables. One potential conce
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The assembly and maturation of invadopodia can be initiated
2020-02-19

The assembly and maturation of invadopodia can be initiated by chemical stimuli such as the epidermal growth factor (EGF), as well as the mechanical signals from extracellular matrix (ECM). Upon binding, EGF activates the EGF receptor (EGFR), which further activates several intracellular signaling p
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br Inhibiting APC C during
2020-02-19

Inhibiting APC/C during Interphase and prior to Anaphase Because ubiquitylation by APC/C triggers cell division, it is essential that APC/C is restrained until cells are prepared for its substrates to be degraded. In addition to regulation by phosphorylation, an additional layer of control comes
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br Concluding remark br Acknowledgements br Detection and re
2020-02-19

Concluding remark Acknowledgements Detection and repair of the numerous, and potentially lethal, DNA lesions arising in human Clofarabine daily is largely mediated by an efficient system collectively termed the DNA-damage response (DDR). Paradoxically, DNA-repair processes within cancer cell
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Findings from the present study indicate that CRF receptors
2020-02-18

Findings from the present study indicate that CRF1 receptors are especially important in fear acquisition. CP154,526 given before acquisition training, at least partly, reinstated the fear-potentiated startle response and blocked the development of contextual conditioned fear in SERT−/− rats. CP154,
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It should be noted that there
2020-02-18

It should be noted that there are other methods, such as artificial intelligence, like Artificial Neural Networks/ANN (such as PSO-ANN, ICA-ANN), Least Square Support Vector Machine/LSSVM, etc. [10], [11], [12], [13], [14], [15], [16], [17], [18], or molecular simulations, for modeling the fluid\'s
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The recombinant Scl collagen system has shown capability as
2020-02-18

The recombinant Scl2 collagen system has shown capability as a biomaterial as well because of its adaptability and scalability. Scl2 was functionalized to crosslink into a hydrogel without disrupting its triple helix [130]. The Scl2–hydrogel crosslinking also did not disrupt cell adhesion and integr
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br Materials and methods br Results
2020-02-18

Materials and methods Results Discussion Inflammatory signalling and in particular the arachidonic BMS-833923 cascade have been suggested as targets for disease modification, optimization of the therapeutic response, and even restoration of pharmacosensitivity (Potschka, 2010). Recently, w
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EBI is known to play
2020-02-18

EBI2 is known to play a critical role in the induction of antibody responses in secondary lymphoid tissues.13, 14 However, little is known about the expression and function of EBI2 in human peripheral tissues. To our knowledge, this is the first report of increased EBI2 levels in peripheral tissues
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In conclusion we have found that Egr can
2020-02-17

In conclusion, we have found that Egr1 can play an inhibitory role on DBH promoter-driven transcription. This inhibition requires a newly identified Egr1 response Pasireotide sale at the −227/−224 region of DBH promoter. This inhibition appears to result from Egr1 directly bound to the DBH promoter
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Introduction Nucleic acids are polyanionic and their
2020-02-17

Introduction Nucleic acids are polyanionic and their negatively charged nucleotides allow the binding of cationic dyes, such as acridine orange (3,6-dimethylaminoacridine). Acridine orange (AO) was first synthesized in 1889, but its ability to bind nucleic acids was only reported in 1940, with grea
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Amyloid β-peptide (10-35), amide The binding pattern of was
2020-02-17

The binding pattern of 1 was analysed by flexible molecular docking. The Amyloid β-peptide (10-35), amide inserted into the narrow ATP binding site of CK2 (Fig. 2). As shown the aliphatic chain of 1 was located at the edge of the pocket and established van der Waals interactions with the side chain
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gsk3 inhibitor Gastrointestinal tone can be effectively modu
2020-02-17

Gastrointestinal tone can be effectively modulated by cholinesterase inhibitors. As parasympathetic fibers release gsk3 inhibitor to contract the circular and longitudinal intestinal muscles, AChE inhibition can facilitate those actions. Postoperative ileus (delayed gastric emptying after surgery) c
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bcrp inhibitor br Loss of Chk sensitizes cells to
2020-02-17

Loss of Chk 1 sensitizes bcrp inhibitor to hypoxia/reoxygenation In contrast to Chk 2, studies have identified Chk 1 as being phosphorylated in an ATR-dependent manner at residue serine 345 during hypoxia [18]. More recently, siRNA mediated inhibition of Chk 1 signaling was found to sensitize cel
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