• br Apelin The APJ receptor ligand

  2023-01-04

  

  Apelin The APJ receptor ligand apelin firstly in 1998 was segregated from bovine stomach tissue. Human preproapelin gene located on chromosome Xq25–26.1. The apelin preproproteins consist of 77 amino SQ 29,548 residues that are cleaved into biologically active C-terminal fragments of various siz

• An unbiased evaluation of hepatic mRNA was performed

  2023-01-04

  

  An unbiased evaluation of hepatic mRNA was performed to assess the impact of hepatocyte AMPK activation on the transcriptome. The expression of 913 genes were altered in control mice after chronic PF-06409577 treatment, 188 genes were affected by knocking out AMPK in hepatocytes, and expression of 2

• br Results and discussion br Conclusion The

  2023-01-04

  

  Results and discussion Conclusion The tyrosine kinase ALK represents one of the most successful molecular targets for the development of precise medicine to treat stratified subgroups of cancer patients. Three generations of ALK inhibitors have been awarded the FDA's approval or are being exte

• As an alternative to chronic receptor blockade we

  2023-01-04

  

  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 Dihydroeponemycin adenosinergic signalling (Boison, 2006, Etherington et al., 2009). Up-regulating ADK faci

• Selumetinib There has been growing interest over computation

  2023-01-04

  

  There has been growing interest over computational methods to predict the biological activity by chemical structure, so as to decide whether it Selumetinib has objective qualities or not. In this contribution, the well-known method, which is called quantitative structure–activity relationship (QSAR)

• The discovery of acetylsalicylic acid aspirin in paved the

  2023-01-03

  

  The discovery of acetylsalicylic MK-8745 (aspirin) in 1897 paved the way for the development of classical NSAIDs as first-line therapeutics for anti-inflammatory, anti-pyretic and analgesic therapy. Large efforts have been made in the following decades to improve the efficacy and in particular safe

• Matthew et al synthesized and carried out SAR studies

  2023-01-02

  

  Matthew et al. synthesized and carried out SAR studies of imidazo-[1,2-a]-pyrazine as Aurora kinase inhibitors with enhanced kinase selectivity and found that Oleandrin mg 39 showed optimal potency on Aurora-A and Aurora-B with IC50 value of 4 nM and 13 nM while on phosphorylation histone H3 (pHH3)

• V ATPase is a complex

  2023-01-02

  

  V-ATPase is a complex enzyme that is composed of several subunits, which are assembled into two domains: trans-membrane (V0) and cytosolic (V1) domains [3,5]. Epididymal epithelial beta 3 agonist of rats has been reported to contain V-ATPase which is distributed at the apical pole of the narrow and

• Recent findings imply that proper Na K ATPase function is

  2023-01-02

  

  Recent findings imply, that proper Na+/K+-ATPase function is crucial for unimpaired development of the vertebrate heart. Targeted knockout of Na+/K+-ATPase α1 in mice led to early embryonic lethality whereas heterozygous knockout mice displayed severe hypocontractile hearts [52]. Pharmacological inh

• The growth of cancer can control by inhibiting the

  2023-01-02

  

  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

• In our study caspase and DRAM were

  2023-01-02

  

  In our study, caspase3 and DRAM were identified as being involved in full-length AIFM1-induced apoptosis. Caspase3 is best known for its role in the execution phase of apoptosis in both intrinsic and extrinsic apoptotic pathways [17]. The members of the caspase family are generally in inactive pro-f

• The reception of antiangiogenic treatment in neuro oncology

  2023-01-02

  

  The reception of antiangiogenic treatment in neuro-oncology has yet to achieve the wide success rapidly accomplished for other malignancies. In 1984, mutated receptor tyrosine kinase became a culprit for aberrant tumorigenesis signal, providing a target for monoclonal Miglitol (mAbs) and small-mole

• br AR signaling and urothelial cancer progression As shown

  2023-01-02

  

  AR signaling and urothelial cancer progression As shown in other types of malignancies, such as prostate cancer cells, it has been documented that androgens induce AR expression and its nuclear translocation as well as ARE promoter activity in urothelial cancer cells (Chen et al., 2003, Izumi et 

• br Experimental section br Results and

  2023-01-02

  

  Experimental section Results and discussion Conclusion Acknowledgement This work was supported by the National Natural Science Foundation of China (Grant Nos. 81401489), the Shanghai Pujiang Program (17PJ1402800) and the Shanghai Sailing Program (Grant No. 14YF1409000). Introduction

• AAT enzyme activity was readily

  2023-01-02

  

  AAT enzyme activity was readily detected in crude cell-free extracts obtained from berry tissues of all accessions but displayed different substrate selectivities (Fig. 2). Cell-free extracts derived from ‘Muscat Hamburg’ berries showed the highest AAT activity with all alcoholic substrates tested,

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