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L-NMMA citrate Phosphoinositide kinase PI K Akt has been
2023-04-11

Phosphoinositide 3-kinase (PI3K)/Akt has been well demonstrated in the protection of myocardial cell against IR injury via increasing cardiomyocyte survival, inhibiting excessive autophagy, et al. (Kong et al., 2016). The L-NMMA citrate of ERK1/2 also involves in the regulation of cardiac myocyte s
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The ambiguity surrounding the role played by
2023-04-11

The ambiguity surrounding the role played by the 15-LOXs in malignant biological processes stems also from the limitations of current animal models, and especially the usage of its 12/15-LOX murine homolog, which can also catalyze the production of 12-HETE. Indeed, the proinflammatory effect of 12-H
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We also show that in both
2023-04-11

We also show that in both ATM proficient and deficient/mutant SB-222200 the activation of ATR signaling is DSB complexity-dependent (Figs. 1, 4A, C and E, 6A and B). Wang et al. have also reported that the effects of ATR and CHK1 on radiosensitivity are independent of the NHEJ repair pathway [41],
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7915 receptor Apelin is involved in various physiological fu
2023-04-11

Apelin is involved in various physiological functions, including 7915 receptor contraction (Ashley et al., 2005), vasodilatation (Jia et al., 2007), feeding control (Valle et al., 2008), and metabolic homeostasis (Higuchi et al., 2007, Dray et al., 2008, Attane et al., 2010). Its plasma level is ele
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Using this cheese mimicking matrix we screened the antifunga
2023-04-11

Using this cheese-mimicking matrix, we screened the antifungal activity of 44 LAB fermented milk-based products and 23 LAB isolates used as protective cultures against 4 fungal targets. The LAB were obtained from the culture collections of CIRM-BIA (Centre International de Ressources Microbienne-Bac
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Fisetin br The lipoxygenase pathway in vascular physiology
2023-04-10

The 12/15-lipoxygenase pathway in vascular physiology and pathology The mammalian 12- and 15-LOXs have high substrate specificity oxidizing predominantly ω−6 (arachidonic and linoleic acids) but also the ω−3 (docosahexanoic) Fisetin [86], [87], [88]. Different LOXs oxidize fatty acids both in the
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br Materials and methods br Results br
2023-04-10

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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br Methods br Results br Discussion Agitation in dementia
2023-04-10

Methods Results Discussion Agitation in dementia has recently been defined as a syndrome characterized by inferred or observed evidence of emotional distress associated with at least one behavioral component, i.e. excessive motor activity, verbal or physical aggression (Cummings et al., 201
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An ALK rearrangement was found in all
2023-04-10

An ALK rearrangement was found in all the analyzable ‘truly positive’ IHC+/FISH+ samples, and the proportion of the various transcripts was in accordance with the literature [[26], [46], [47], [48]]. In these samples, the RNA-seq technique was therefore 100% sensitive and specific. Additional non-ta
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The co crystal structure of blebbistatin bound to
2023-04-10

The co-crystal structure of ()-blebbistatin ()- bound to myosin II (PDB: ) was used to scout for possible favorable interactions with the residues lining the binding pocket. Looking at A, we hypothesized that -oriented hydrophilic moieties (e.g. hydroxymethyl) on C of the blebbistatin scaffold might
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Several studies have demonstrated that depletion of function
2023-04-10

Several studies have demonstrated that depletion of functional ATR increases the sensitivity of cancer cells to oncogene-induced replication stress thereby hindering tumour growth and inducing extensive cell death (Gilad et al., 2010, Murga et al., 2011, Schoppy et al., 2012). Importantly, Schoppy e
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Several structural classes of ASK inhibitors mostly
2023-04-10

Several structural hyPerFUsion™ high-fidelity PCR Kit of ASK1 inhibitors, mostly from industry but also from academia, have been identified over the last decade. In 2012, Terao et al. (Takeda) reported imidazo[1,2-α]pyridine () as a potent ASK1 inhibitor derived from structure-based drug design. G
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Introduction Antimicrobial resistance is a growing health
2023-04-10

Introduction Antimicrobial resistance is a growing health threat worldwide that has been associated with incorrect prescription and overuse of Tiopronin mg [1]. Considering that physicians play a central role in antibiotic usage, a better understanding of their prescribing behaviours and their kno
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br Antibiotic drug discovery approaches Traditionally novel
2023-04-10

Antibiotic drug discovery approaches Traditionally, novel Hordenine were largely discovered by phenotypic screening approaches of various sources of compounds, such as natural products isolated from extracts of soil microbes and semi-synthetic or fully synthetic compound libraries derived from kn
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br HIF Blockade in AA Therapy
2023-04-10

HIF-α Blockade in AA Therapy In lieu of the evidence supporting a central role for HIF-α signaling in tumor angiogenesis and CC pathobiology, significant efforts have focused on the discovery of small-molecule HIF-α inhibitors (for exhaustive compendia, see [28,44,45]). In brief, inhibitors vary
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