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The widespread involvement of HH GLI in human malignancies h
2022-03-09

The widespread involvement of HH/GLI in human malignancies has initiated a remarkable effort to identify selective HPIs. As shown in Table 2.1, most of these small molecule inhibitors target the essential effector protein SMO, which should lead to pathway abrogation by eventually decreasing the GLIA
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Amongst oxidants that we have studied PMS is unique
2022-03-09

Amongst oxidants that we have studied, PMS is unique in having a greater effect in deoxygenated cells. The resulting phenotype shows some similarities with the increased cation permeability shown by deoxygenated sickle Genomic DNA Isolation Kit mg [27]. It is interesting to consider why PMS has thi
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In addition to attenuating joint inflammation via
2022-03-09

In addition to attenuating joint Tofacitinib Citrate mg via T cells, Cpd43 could also decrease the severity of CIA/AIA by suppressing the function of innate leukocytes such as neutrophils and macrophages via FPRs, as has been shown in other acute inflammatory models including neutrophil/macrophage-
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br G protein coupled receptor GPR also
2022-03-09

G-protein coupled receptor 40 (GPR40), also known as a free fatty birinapant receptor, is dominantly expressed in pancreatic β cells and intestine K, L cells., . Besides, GPR40 is also reported to be expressed in brain, but its function is still unknown. It is well documented that GPR40 agonist i
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Colorectal cancer CRC is the
2022-03-09

Colorectal cancer (CRC) is the leading cause of cancer deaths in Taiwan and is also a most common cancer in the world (Huang et al., 2012, Jemal et al., 2011). With early detection and treatment in the initial stage, CRC can be recognized as curable in comparison with other malignant tumors (Levin e
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br Acknowledgments I thank Takeshi Sakaba for
2022-03-09

Acknowledgments I thank Takeshi Sakaba for critical reading of the manuscript and helpful comments. This work was supported by JSPS/MEXT KAKENHI Grant Numbers 17K19466, 17H03548. Introduction The oral route of drug application is the main route in pharmacology since it is easy to handle and o
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Several recent studies have linked clock function
2022-03-08

Several recent studies have linked clock function with the cell cycle and reported that clock components, such as PER1, PER2, BMAL1, and CRY1/2 decrease cell proliferation or improve the action of anti-cancer drugs in different cancer cell lines. Moreover, certain types of human cancer show an alter
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br Acknowledgements br Introduction Pregnancy brings forth s
2022-03-08

Acknowledgements Introduction Pregnancy brings forth significant metabolic reprogramming that induces a number of metabolic changes to ensure that the nutrient requirements of the mother and fetus are met [[1], [2], [3]]. These adaptations change radically over the period of pregnancy dependin
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One of the key epithelium derived
2022-03-08

One of the key epithelium-derived factors required to maintain immune tolerance in the intestine is Indian Hedgehog (Ihh). Ihh is secreted exclusively by intestinal epithelial cells, and signals in a paracrine manner to the inhibitory receptor Patched1 (Ptch1) on Sennoside C in the mesenchyme. Bin
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The rationale for developing HDACi
2022-03-08

The rationale for developing HDACi as anticancer agents was based on their ability to induce the hyperacetylation of histones and nonhistone proteins, resulting in increased differentiation, apoptosis, and SCF, murine recombinant protein arrest of cancer cells 1, 2, 3. HDACi have been used in the tr
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br Trifluoromethylketones This group of compounds was demons
2022-03-08

Trifluoromethylketones This group of compounds was demonstrated to bind the zinc Fluoxymesterone in the active site due to its easy hydration, forming the required chelating intermediate. Ontaria et al. [92] have proposed variations around the cap group of trifluoromethylthiophene as the core mo
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br Conclusions br Introduction Astrocytes
2022-03-08

Conclusions Introduction Astrocytes contribute to physiological SB 290157 trifluoroacetate salt function on many levels. They help maintain the physiological composition of the extracellular medium by, for instance, buffering potassium and uptake of neurotransmitters. They can also provide ne
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br Cholecystokinin CCK CCK is secreted by
2022-03-08

Cholecystokinin (CCK) CCK is secreted by enteroendocrine I-cells of the duodenum and jejunum in response to amino acids and lipids [14]. There are two forms of the CCK receptor, CCK1 which is expressed on pancreatic α- and β-cells while CCK2 is located on somatostatin-secreting δ-cells [8]. CCK r
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Previously we reported that the inhibition of PKC
2022-03-08

Previously, we reported that the inhibition of PKC-ζ and PKC-ε activity in hypertrophic adipocytes had deleterious effects on EPA-induced GPR120-mediated VEGF-A production [12]. However, the activation of PKC-θ, -ζ and -λ can also enhance the phosphorylation of IKK and p65, and facilitate the transl
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In recent years several DPP IV inhibitors
2022-03-08

In recent years, several DPP-IV inhibitors have already been approved, such as sitagliptin, vildagliptin, saxagliptin, tenegliptin, alogliptin and linagliptin, etc. Among them, linagliptin (1, Fig. 1) is a non-peptide mimetic MJ33 lithium salt with a unique xanthine scaffold developed through high-
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