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br Acknowledgements This study was funded the Irish
2025-01-07
Acknowledgements This study was funded the Irish Department of Agriculture, Food and the Marine through the research program FIRM/RSF/CoFoRD (Reference: 13 F 462). The authors declare no conflict of interest. Introduction Radiotherapy (RT) is one of the major treatment methods among patients
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This study demonstrates numerical alterations of creatinine
2025-01-07
This study demonstrates numerical alterations of creatinine levels potentially reflecting ongoing or even higher myocardial contraction of the LAA after successful LAAC. Creatinine is the direct breakdown product of creatine in muscle, the key metabolite for energy supply during muscular and myocard
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Digoxigenin-11-dUTP br Materials and methods br Results and
2025-01-07
Materials and methods Results and discussion Conclusions In this study, for the first time to the best of our knowledge, the stability of pure hsALDH has been studied under various conditions. The enzyme exhibited low storage stability both at 4°C and 25°C, which could be improved to a good
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Long R3 IGF-1 br Hypoadiponectinemia in metabolic syndrome A
2025-01-07
Hypoadiponectinemia in metabolic syndrome APN belongs structurally to the complement 1q family and is found at high concentrations (>0.01% of total protein) in the serum of healthy individuals [6]. Given the abundance of APN in plasma, it is assumed that alterations in plasma levels of APN might
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edaravone dexborneol br The MIR The MIR is defined by the ab
2025-01-07
The MIR The MIR is defined by the ability of a single rat mAb to muscle or electric organ AChRs, typically mAb 35, to block binding of half or more of autoantibodies in human MG or EAMG [44], [45], [46]. Antibodies to the MIR are pathologically significant because they exhibit all the major patho
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Molecular docking is widely used to predict
2025-01-07
Molecular docking is widely used to predict the interaction between an enzyme and its inhibitors. This is a computational simulation approach that can be used as a tool to investigate the structure-activity relationship of ACE inhibitory peptides (Goodsell, 2009). It has been recently shown that ACE
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br AD and COX LOX pharmacology
2025-01-07
AD and COX/5-LOX pharmacology Early studies on the role of cyclooxygenases in AD were inspired by epidemiological data suggesting that COX inhibitors such as nonsteroidal anti-inflammatory drugs (NSAIDs) could be beneficial in AD patients (Lucca et al., 1994, McGeer et al., 1990). This line of re
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Caffeic acid dihydroxycinnamic acid is a natural compound
2025-01-07
Caffeic 597 mg (3,4-dihydroxycinnamic acid) is a natural compound that inhibits 5-LO and exerts potent anti-inflammatory and antioxidant properties. Recently, Takeda et al. reported that caffeic acid provided neuroprotective and anti-depressive activities [23]. Sertraline, a selective serotonin reu
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br Results and discussion br Conclusion In summary a series
2025-01-06
Results and discussion Conclusion In summary, a series of indazole-based derivatives were synthesized and SAR studies conducted, with view to the development of a novel Aurora kinases inhibitor. The carboxylic gpr120 agonist group extending from the C-3 position of the aniline and substituted
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br Autophagy inducers Macroautophagy is often seen
2025-01-06
Autophagy inducers Macroautophagy is often seen as a cellular process capable of increasing the fitness of 2-Dimethylaminoacetaldehyde hydrochloride and overcome resistance to several forms of stress [9], [10]. As discussed above, it has been proposed by several authors that an effective strategy
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We also explored the possibility that this PKC
2025-01-06
We also explored the possibility that this PKC-θ activating protein could operate on the auto-phosphorylation process of the kinase, a specific event accompanying PKC activation [32]. The heated PKC-θ immunoprecipitate from metaphasic cells was then added to PKC-θ isolated both from interphasic or m
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Numerous investigators have shown that RACK has several impo
2025-01-06
Numerous investigators have shown that RACK1 has several important, possibly related, roles in mRNA splicing and in translation. RACK1 interacts directly with specific components of the 40S ribosomal subunit (specifically, the 18S rRNA and ribosomal proteins rpS16e, rpS17e, and rpS3e [new names: uS9
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br AR mediated actions in cells
2025-01-06
AR-mediated actions in Long R3 IGF-1 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 el
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br Understanding AD through Transcriptome Analysis
2025-01-06
Understanding AD through Transcriptome Analysis Both classical gene discovery and pathway-based analysis of AD GWAS shed light on the range of biological processes that contribute to AD in addition to amyloid pathology. The straightforward interpretation and functional investigation of the assoc
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As an alternative to chronic receptor blockade we have been
2025-01-04
As an alternative to chronic receptor blockade, we have been targeting adenosine kinase (ADK) – an astrocyte-based enzyme that catalyses the phosphorylation of adenosine, as a means to modify MRS1523 adenosinergic signalling (Boison, 2006, Etherington et al., 2009). Up-regulating ADK facilitates th
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