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Previously published data showed an interaction
2020-11-05
Previously published data showed an interaction of α-tubulin and CK1δ [15] that was validated in the present study using SPR (Fig. 1A). The dominant motifs involved in the CK1δ/α-tubulin interface were defined using a peptide library of peptides covering the CK1δ amino BAY 80-6946 sequence (Suppleme
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The mechanism underlying the increased PON levels found
2020-11-05
The mechanism underlying the increased PON1 levels found in greenhouse workers may be accounted for by an increased protein PD123319 following pesticide interaction with different nuclear receptors as also occurs with other chemicals, such as polyphenols and statins [28]. A number of nuclear recept
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In conclusion our findings suggested that EP receptor activa
2020-11-05
In conclusion, our findings suggested that EP4 receptor activation triggers apoptosis in B-cell lymphoblasts. Our results also showed that EP4 receptor engagement inactivates NF-κB, which, in turn, sensitizes Ramos RSL3 to apoptosis induced by chemotherapeutic agents. EP4 receptor agonists are curr
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br Results and discussion The effects of hypoxia a combinati
2020-11-05
Results and discussion The effects of hypoxia, a combination of shear stress and hyperoxia, and a combination of shear stress and hypoxia in BAECs were assessed at 0, 15, 30, 60, 120, and 180 min. Changes in phosphorylation levels of eNOS at Ser635 were investigated using immunoblotting, and repr
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Recent reports revealed that CSE affects
2020-11-05
Recent reports revealed that CSE affects the endothelial cells of various tissues like kidney, liver, heart including STK393606 [26,30]. The damage of brain endothelial cells enhances the progress of cognitive dysfunction due to the accumulation of toxic free bio-radicals and activation of inflamma
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CYP A and CYP D are among the main drug
2020-11-05
CYP3A4/5 and CYP2D6 are among the main drug-metabolizing enzymes in humans that are responsible for the metabolism of more than 50% of marketed drugs [19], [21]. Drugs metabolized by CYPs are prone to drug–drug interactions, thereby modifying their response [18], [32]. Metabolic inhibition is also i
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A growing number of other post translational modifications a
2020-11-05
A growing number of other post-translational modifications are implicated in regulation of the ubiquitin system, including substrate modification by hydroxylation, glycosylation, acetylation, methylation, modification by poly(ADP-ribose) (PAR), and attachment of ubiquitin-like modifiers. The HIF1-α
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Consistent with the known tolerance of the Suzuki Miyaura
2020-11-05
Consistent with the known tolerance of the Suzuki–Miyaura reaction to a wide range of aryl substituents, we subsequently found that the commercially available 3-hydroxyphenylboronic Cy5 TSA Fluorescence System Kit pinacol ester () could be coupled to , to give directly and in comparable yield. Smo
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The involvement of FOXO and STAT
2020-11-05
The involvement of FOXO3 and STAT5 in DNA-PKcs and Solamargine IV has not been reported before, and the search by the ECR browser (http://ecrbrowser.decode.org) revealed that 1kb of the 5′ promoter of DNA-PKcs possesses 4 STAT (−908bp to −901bp, −676bp to −656bp, −533bp to −526bp and −66bp to −59bp
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In addition to its HEAT repeats
2020-11-05
In addition to its HEAT repeats, CRM1 also possesses a C-terminal extension (C-extension, residues 1032–1071), composed of a helix (C-helix) followed by a short stretch of residues (C-tail). In the absence of Ran, the C-extension adopts a conspicuous conformation that bridges across the ring-shaped
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Based on the finding described above the present study
2020-11-05
Based on the finding described above, the present study was designed to investigate the effects of specific CRF receptors, CRF1 and CRF2, in the BLA and CeA on the duration of TI in guinea pigs (Cavia porcellus). To this end, we evaluated whether administration of the CRF1 myc pathway antagonist CP-
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Early studies from the mollusk Aplysia reported
2020-11-05
Early studies from the mollusk, Aplysia, reported the presence of a unique class of BMS-707035 receptors in neurons, the acetylcholine-gated chloride channels (ACCs) (Kehoe and McIntosh, 1998). Later, studies identified these receptors in the model nematode Caenorhabditis elegans (Putrenko et al.,
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The presence of a vicious cycle established between tumor
2020-11-05
The presence of a “vicious cycle” established between tumor proliferation and paratumor osteolysis plays a crucial role in the development of primary bone tumors [53]. Cancer cells produce soluble factors that activate directly or indirectly via osteoblasts, osteoclast differentiation and maturation
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I bungarotoxin competes with ACh an endogenous
2020-11-04
[125I] α-bungarotoxin competes with ACh, an endogenous activator of α7-nACh receptors by binding to the ACh binding site on the receptor (Albuquerque et al., 2009). For this reason, the effect of curcumin was investigated on the specific binding of [125I] α-bungarotoxin. Saturation curves for the bi
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special info Previous studies demonstrated that cPLA translo
2020-11-04
Previous studies demonstrated that cPLA2α translocates to the phagosomal membrane during macrophage phagocytosis through mechanisms that, in humans, involve phosphorylation of the enzyme by c-Jun N-terminal kinases and membrane association via the cationic cluster of four lysine residues present at
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