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Thus far clinical data indicate that IDO inhibitors have man
2022-12-15
Thus far, clinical data indicate that IDO1 inhibitors have manageable toxicity, albeit with a relatively short period of treatment in a small number of patients. KYN is a pluripotent mediator and key intermediate for the synthesis of a host of downstream KP metabolites that are implicated in inflamm
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The lanthanide series of chemical elements comprises the fif
2022-12-15
The lanthanide series of chemical elements comprises the fifteen metallic chemical elements with atomic numbers 57 through 71, from lanthanum to lutetium. Though originally described as ‘‘rare earths’’ because of their natural occurrence as metal oxides, they are not particularly rare. The lanthanid
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CYP A is one of the key metabolizing
2022-12-15
CYP3A4 is one of the key metabolizing Cy5.5 maleimide (non-sulfonated) of the cytochrome P450 (CYP) superfamily of heme-containing monooxygenases. As the CYP family of enzymes plays important roles not only in the xenobiotic metabolism and detoxification of a large number of drugs, but also in the b
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ICG001 synthesis br Materials and methods br Results br
2022-12-15
Materials and methods Results Discussion Numerous studies showed that Na+-K+-ATPase activity and membrane ICG001 synthesis were decreased in cardiac tissue subjected to IR (Belliard et al., 2013; Lee et al., 2013). In return, treatment that alleviated the progress of IR-related myocardial
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Apelin APJ triggers a variety of cellular
2022-12-14
Apelin/APJ triggers a variety of cellular signaling pathways (Fig. 1). Recent studies from our laboratory showed that apelin-13 induces vascular smooth muscle cell (VSMC) proliferation by the upregulation of Cyclin D1 expression, which is involved in an ERK-dependent activation of Jagged-1/Notch3 si
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The PDZ domains of DLG
2022-12-14
The PDZ domains of DLG interact with tumor suppressor proteins, APC and PTEN, as well as with several viral oncoproteins such as the E6 protein present in oncogenic human papillomavirus (reviewed in [177]). It has been reported that overexpression of DLG in fibroblasts impairs the events in the G0/G
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What are the in situ effects of multi site
2022-12-14
What are the in-situ effects of multi-site CaM associations with AT1R? Kai et al. showed that synthetic peptides corresponding to residues 125–137 (rat sequence) in SMD2, 217–227 in the N-terminal side of SMD3, and 304–316 in SMD4JM inhibit to various degrees AngII-induced GTPase activity of isolate
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Recent retrospective cohort studies have
2022-12-14
Recent retrospective cohort studies have supported these preclinical findings in animals indicating the correlation of AR activation with the induction of 1215 carcinogenesis. First, men with prostate cancer who underwent androgen deprivation therapy were shown to have a significantly lower risk of
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Circular dichroism CD provides useful information about prot
2022-12-14
Circular dichroism (CD) provides useful information about protein structure, the extent and rate of structural changes and ligand binding. CD is a form of light 5-lipoxygenase spectroscopy that measures differences in the absorbance of right- and left-circularly polarized light (rather than the com
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br Materials and methods br Results br Discussion
2022-12-14
Materials and methods Results Discussion The novel and central finding of the current study is that endothelial 12/15-LO rather than the monocytic/macrophagic 12/15-LO has a critical role in hyperglycemia-induced leukocyte adhesion and retinal endothelial barrier dysfunction. The following
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Recent genome wide association studies have indicated SORL a
2022-12-14
Recent genome-wide association studies have indicated SORL1 as a risk factor for AD (Meng et al., 2007, Rogaeva et al., 2007, Wen et al., 2013). SORL1, is expressed in neurons (Yin et al., 2015) and also regulates APP traffic from the cell membrane to the Golgi apparatus. A reduction in its expressi
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Alectinib is a second generation ALK antagonist that
2022-12-14
Alectinib is a second generation ALK antagonist that is built upon a 9-ethyl-6, 6-dimethyl-11-oxo benzo[b]carbazole scaffold (Fig. 5C) [58]. This drug is effective against the ALK L1196M gatekeeper mutation along with C1156Y and F1174L mutations [7]. The 11-oxo group of the drug forms a SCH727965 w
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Recently rather than predicting categorical
2022-12-14
Recently, rather than predicting categorical variables as in classification, several studies begin to estimate continuous clinical variables from eplerenone cost images. Therefore, instead of classify a subject into binary or multiple pre-determined categories or stages of the disease, regression f
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It is reported that Adiponectin is able to suppress NF
2022-12-14
It is reported that Adiponectin is able to suppress NF-κB pathway, and Bcr-Abl fusion oncoprotein in CML activates NF-κB by stimulating its nuclear translocation and also by enhancing its transactivation function [25], [26]. Therefore, it is tempting to hypothesize that NF-κB pathway might be involv
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Protein blast analysis of the sequence of globin B
2022-12-14
Protein blast analysis of the sequence of globin-B with those of other PP 2 suggests that the globin-B domain in the HemAC-Lm displays only 6% identity and 34% similarity with that of cytoglobin/neuroglobin (Fig. 2). Furthermore, SWISS-MODEL protein modeling also predicts that the His311 is the prox
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