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Amyloid fibrils are insoluble high molecular weight non crys
2025-02-25

Amyloid fibrils are insoluble, high-molecular-weight, non-crystalline aggregates and traditional experimental techniques for structure determination such as X-ray and solution NMR cannot resolve their high resolution structures [64], [68]. However, amyloid fibrils exhibit various advantageous featur
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br Concluding Remarks and Future Perspectives
2025-02-25

Concluding Remarks and Future Perspectives The collective evidence from studies detailing the functions of AMPK in the neuromuscular system, combined with those in DMD, SMA, and DM1 surveyed in the present review, strongly suggests that AMPK is a central mediator of neuromuscular determination, m
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Dose Response Studies Against Puromycin Sensitive Aminopepti
2025-02-25

Dose–Response Studies Against Puromycin–Sensitive Aminopeptidase (PSA). PSA is a ubiquitous metallopeptidase encoded by the NPEPPS gene with subcellular distribution in the cytosol and nucleus [49]. Comprising of a 919 amino all trans retinoic acid sequence, it has a broad substrate specificity, an
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One study has demonstrated that
2025-02-25

One study has demonstrated that ω-3 PUFA reduced both cholesterol and caveolin-1 (a marker of raft), thereby displacing raft-associated signaling molecules from lipid raft [36]. Additionally, DHA treatment decreased the amount of lipid raft in the cell surface and displaced several lipid raft-associ
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exemplifies three of the compounds investigated in the selec
2025-02-24

exemplifies three of the compounds investigated in the selection for a candidate drug (CD). Our first criteria was an IC Ro3306 as such did not show any genotoxicity in the SOS/umu assay, but this does not say anything about any possible genotoxicity of its metabolites or degradation products. As BL
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Treatment of all of the GYN cancer
2025-02-24

Treatment of all of the GYN cancer PHA-767491 in this study with ATRi not only reduced phosphorylation of Chk1 at Ser345 following genotoxic stress, but also phosphorylation of ATM. Loss of phospho-ATM following ATRi treatment is not likely due to non-specific targeting of ATM by ETP-46464 [28]. Whi
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TLX may promote survival and prevent apoptosis in NB
2025-02-24

TLX may promote survival and prevent apoptosis in NB methysergide [12]. Here, we ask whether the survival-promoting effects of TLX are mediated by Apoptosis Signal-regulating Kinase-1 (ASK1, MAP3K5). ASK1 is a member of the Mitogen-Activated Protein (MAP) kinase family and it preferentially activate
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The growth of cancer can control by inhibiting the
2025-02-24

The growth of cancer can control by inhibiting the rate of cell proliferation or increasing the rate of selective apoptosis and effectiveness of anticancer agents varies according to genetic constitution of cancer. Hence, we investigated the anticancer activity of arginase against different kinds of
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Arginases from several species and
2025-02-24

Arginases from several species and tissues have been found to be inhibited by amino acids [51]. In the present study, monocarboxyilic amino acids with five or more carbon atoms such as ornithine, lysine, valine, leucine and isoleucine inhibited CL-ARG. The results revealed that as the amino ixabepil
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BAMB-4 br Antioxidant polymers conjugates Natural antioxidan
2025-02-24

Antioxidant-polymers conjugates Natural antioxidants are usually used as a substitute for synthetics but some degradation phenomena could influence their applications. For example, ascorbic BAMB-4 as a natural antioxidant undergoes yellowish coloration as a result of oxidation [29]. Sing and Kapl
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It is worth noting that in S cerevisiae the control
2025-02-24

It is worth noting that in S. cerevisiae, the control of two cell-cycle checkpoints requiring Mcm1 involves two very different mechanisms. At the G1/S transition, Mcm1 transactivation activity is inhibited by Yox1 and Yhp1 repressors, whose expression is periodically regulated through the cell cycle
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Using the same techniques we found that UCP
2025-02-24

Using the same techniques, we found that UCP3 also has a half-life of between 1 and 4h [117]. In eplerenone cost to UCP2 and UCP3, UCP1 and ANT had much longer half-lives and could not be degraded in the cell-free reconstituted system, suggesting their degradation is not mediated by the cytosolic pr
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Glycosylphosphatidylinositol GPI cell wall anchor synthesis
2025-02-24

Glycosylphosphatidylinositol (GPI) NMS-E973 anchor synthesis pathway is another promising antifungal target. Novel inhibitors of Gwt1 and Mcd4, two enzymes in the GPI anchor pathway were identified by the chemical-genomics-based screening platform CaFT (Candida albicans fitness test) [89]. Screenin
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Cisplatin The proinflammatory cytokines and chemokines
2025-02-24

The proinflammatory cytokines and chemokines, including IL-1β, TNF-α and MCP-1, mediate acute and chronic inflammation and play a role in the development of hypertension [2, [51], [52], [53]], cardiovascular diseases [4, 54] and renal injury [55, 56] in animal models and humans. Concerning the possi
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br AR mediated actions in cells
2025-02-24

AR-mediated actions in BIBW2992 of the vascular wall Sex hormones may influence the size and composition of atherosclerotic lesions indirectly by modifying systemic cardiovascular risk factors such as plasma lipids profiles and insulin sensitivity; this aspect of their action is discussed elsewhe
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