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Z-WEHD-FMK receptor br Disclosure br Acknowledgement br
2024-11-11
Disclosure Acknowledgement Introduction CYP17A1 is a multifunctional enzyme with both 17α-hydroxylase and 17,20-lyase activities and is essential for the biosynthesis of steroidal Z-WEHD-FMK receptor in male testes and adrenal glands. The 17α-hydroxylase activity of CYP17A1 is involved in t
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As mentioned above variation of the A ring was undertaken
2024-11-11
As mentioned above, variation of the A-ring was undertaken in order to improve microsomal stability and kinase selectivity relative to Caspase-3/7 Inhibitor (). 1-Imidazole-2-carboxamides with substitution at the 4-position (–) were mostly tolerated with 4-cyano-imidazole-2-carboxamide () having co
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hsp70 inhibitor br Introduction S http www
2024-11-11
Introduction Systemic lupus erythematosus (SLE) is a group of systemic autoimmune disorders characterized by anti-nuclear hsp70 inhibitor (ANA), rashes and photosensitivity, joint inflammation, nephritis, and other clinical criteria. SLE develops through the breakdown of three major checkpoints:
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leukotriene receptor antagonists To help ensure the fidelity
2024-11-11
To help ensure the fidelity of mitosis and cytokinesis cells monitor these processes and delay cell cycle progression in response to certain defects. The spindle assembly checkpoint (SAC) is a surveillance system which delays leukotriene receptor antagonists onset until a bipolar spindle has been co
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Zhang et al screened three thousand compounds
2024-11-11
Zhang et al. screened three thousand compounds library and found two active 3,5,6-substituted indolin-2-one molecules. Further, they designed various derivatives of this scaffold and among them compound 23 from the series was found active with 1.8 μM on Aurora-B kinase luminescent assay [53]. Jeffe
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br Materials and Methods br
2024-11-11
Materials and Methods Results Discussion 15-HETE is a predominant eicosanoid in pulmonary vascular remodeling, and it could promote hypoxia-induced PAH via its involvement in the regulation of proliferation and cell cycle progression in PASMCs. To understand its role in HPH, we have previou
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br The role of LOX plays in
2024-11-11
The role of 12/15-LOX plays in autophagy Autophagy is a process by which cellular material is delivered to lysosomal to degrade the damaged organelles and proteins to facilitate nutrient recycling (Towers and Thorburn, 2016). There has been characterized three types of autophagy-macroautophagy, m
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br Conclusion We present here
2024-11-11
Conclusion We present here the first comprehensive analysis of B-Raf-induced transcriptional activation in insulinoma cells. The B-Raf-induced signaling cascade targets the c-Fos and the c-Jun genes. Both gene products are constituents of the AP-1 transcription factor. The phosphatases MKP-1 and
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br Acknowledgement br Introduction Estrogens play an
2024-11-11
Acknowledgement Introduction Estrogens play an important role in the development and progression of breast cancer (McGuire et al., 1976; Clemons and Goss, 2001). 17β-Estradiol (E2), the most biologically active estrogen in breast tissue, functions via its nuclear receptors, estrogen receptor (
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Ala a branched chain amino acid
2024-11-11
Ala, a branched chain amino acid, has been reported to play a functional role in intracellular pH regulation, and it typically accumulates in response to various stresses (Limami et al., 2008, Rocha et al., 2010). Our data demonstrated that increasing Cd concentrations at lower Cd doses resulted in
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GSK343 In conclusion phenolic hydroxyl was introduced not on
2024-11-11
In conclusion, phenolic hydroxyl was introduced not only to C3 side chain but also to C6 or C7 position of the quinoxalinone core, resulting in a new group of ARIs candidates exhibiting antioxidant activity. Biological activity tests suggested that compounds were not only sufficient to inhibit ALR2
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Ginsenosides are the major bioactive constituents
2024-11-11
Ginsenosides are the major bioactive constituents of the Panax ginseng root, which contain many types of ginsenosides including Rb1, Rg1, Rc, and Rg3. The ginsenoside Rb1 appears to be the most abundant of the bioactive ginsenosides [15]. Rb1 exhibits antiinflammatory, anticarcinogenic, and antioxid
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APPL was the first adaptor protein identified that interacts
2024-11-09
APPL1 was the first adaptor protein identified that interacts directly with adiponectin receptors [18]. A two-hybrid study by Dong and colleagues revealed that the C-terminal extracellular domain of AdipoR1 interacts with adiponectin, whereas the N-terminal cytoplasmic domain of AdipoR1 interacts wi
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Active SI behavior was dose dependently affected by
2024-11-09
Active SI behavior was dose-dependently affected by PACAP treatment (F3,25 = 14.42, p Fosmidomycin sodium salt receptor 1 week later (F3,20 = 8.93, p in the 1-week test (Figure 2F). Although there was a main effect of treatment (F3,20 = 4.29, p hypothesis that PACAP causes disruptions in posterror
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G actin has a molecular weight of
2024-11-09
G-actin has a molecular weight of 42 kD and dimensions about 55 × 55 × 35 Å3. It consists of 375 amino acids arranged into two individual domains (Alberts et al., 2014). A central cleft bisects the protein into two aforementioned domains which surround a deep cleft containing ATP or ADP and a tightl
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