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There are in contrast many studies demonstrating
2024-12-24
There are in contrast many studies demonstrating that sex steroids modulate Modified CTP for DNA synthesis processing of stimuli related to reproduction and this correlates with the observation that steroid receptors and aromatase are expressed in many brain nuclei that are part of the olfactory, v
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Estrogen exerts its genomic action via estrogen
2024-12-24
Estrogen exerts its genomic action via fxr agonist nuclear receptor: ERα and ERβ. The distribution of ERα and/or ERβ positive neurons in CNS of different species has been mapped extensively by various methods [41], [42], [43], [44], [45], [46], [47], [48], [49], [50], although there are some differ
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We further evaluated the possibility whether letrozole media
2024-12-24
We further evaluated the possibility whether letrozole mediates its effect through diverting the pathway towards 5α-DHT and further to 3α-Diol. For this purpose, we measured the concentrations of 5α-DHT and 3α-Diol in mice hippocampus and found that letrozole elevated both 5α-DHT and 3α-Diol levels
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br Concluding remarks It is clear that a disordered
2024-12-24
Concluding remarks It is clear that a disordered l-arginine homeostasis by changes in arginase, NOS and ADMA activity and expression, is not only vital in the chronic airway diseases, BMX-IN-1 and COPD, but also seems to play an important role in many co-morbidities. Unknown, however, is whether
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br Implications for cancer ROS have a long history
2024-12-24
Implications for cancer ROS have a long history of being involved in the development and progression of cancer and increased ROS level is considered as a hallmark of many tumors [76], [77]. Initially, it was thought that ROS would serve as chemical mutagens that would indiscriminately damage cell
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Introduction Alzheimer s disease AD is
2024-12-24
Introduction Alzheimer's disease (AD) is a complex neurological disorder characterized by a progressive dementia resulting from synapse failure (Selkoe, 2002, Tanzi, 2005). The amyloid hypothesis maintains that the pivotal event in AD is the production of amyloid-β (Aβ) peptides following the prote
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Considering our previous results with cfDNA in EGFR TKI
2024-12-24
Considering our previous results with cfDNA in EGFR TKI-resistant NSCLC patients and growing evidence about different mutations in the ALK kinase domain as responsible for acquired resistance to ALK TKIs, we planned this study. Even if a next-generation sequencing approach after PD during crizotini
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Lee et al have demonstrated
2024-12-24
Lee et al. have demonstrated that APPL1 associates with AdipoR1 in Hek293 chondroitin sulfate glucosamine where both proteins have been overexpressed with suitable tags [16]. In contrast to recent data the formation of this complex is not enhanced by exogenous adiponectin [16], [33]. Knock-down of A
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celecoxib The subdivision of HT receptors started in the s
2024-12-24
The subdivision of 5-HT receptors started in the 1950s by Gaddum and colleagues, when they realised that in the guinea pig ileum, the effects of 5-HT could be blocked in part by morphine (M), and in part by dibenzyline (D). Gaddum and Picarelli proposed two receptor classes, 5-HT M and 5-HT D (1957)
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The exact etiology of BPH is not completely understood howev
2024-12-23
The exact etiology of BPH is not completely understood, however this pathology has been associated with elevated TPO-R agonist levels of the androgen DHT (10). Thus, a valuable strategy in BHP treatment is the reduction of DHT (10) levels, by inhibiting its biosynthetic production [6], [8]. An impo
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An AXL decoy receptor with
2024-12-23
An AXL decoy receptor with enhanced GAS6-binding properties, MYD1, was engineered as a therapeutic tool to disrupt GAS6/AXL signaling in vivo (Kariolis et al., 2014). MYD1 was shown to block metastasis of human ovarian cancer deucravacitinib and a murine breast cancer cell line in grafting assays i
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Here we report discovery of highly selective pan Aurora kina
2024-12-23
Here we report discovery of highly selective pan-Aurora kinase inhibitors through phenotypic screening. The co-crystal structure of KN-92 hydrochloride bound in the ATP binding site of Aurora A is described, and provides insight into the possible structural basis for the selectivity of the interac
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br Oxidative microbe killing and V ATPase
2024-12-23
Oxidative microbe killing and V-ATPase Oxidative killing of phagocytosed microorganisms is predominately achieved through the uptake of large quantities of molecular oxygen by the infected cell and the activity particularly of the NADPH oxidase complex on phagosomes (Savina et al., 2006) and the
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Epigenetic modulator br Experimental section br Competing in
2024-12-23
Experimental section Competing interests Author's contributions Acknowledgement This research is partially supported by a seed fund for the Center for Drug Discovery and Translational Research (LS) and a research grant by Fujifilm (VPS and LS). The Sponsors played no roles in study desig
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The LOX hydroxide metabolites are converted to secondary
2024-12-23
The 15-LOX hydroxide metabolites are converted to secondary lipid mediators such as lipoxin A4 from 15-HETE and protectin D1/resolvin D1 from 17-HDoHE [45] (Fig. S3). Importantly, all of these secondary lipid mediators have anti-inflammatory and pro-resolving properties [46], [47], [48]. Lipoxin A4
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