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          DGAT-1 inhibitor australia In the Medicines for Malaria2021-11-15  In 2011 the Medicines for Malaria Venture (MMV) distributed the Open-Access Malaria Box to accelerate antimalarial drug discovery (Spangenberg et al., 2013). The Malaria Box consists of 400 structurally diverse compounds, curated from >20,000 hits generated from large-scale screens, that inhibit the 
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          br Introduction The period around birth2021-11-15  Introduction The period around birth is a risky time for stroke in infants. Ischemic stroke has been diagnosed in about 1/4000 full-term infants (Nelson and Lynch, 2004) and perinatal stroke represents the second most frequent cause of acute seizures in this age group (Levy et al., 1985). Further 
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          In addition to indoles two additional structural variants2021-11-15  In addition to indoles –, two additional structural variants were synthesized to explore the synthetic flexibility and structure–activity relationships of this system. The first of these was the homologation of the acetic LX-1031 side chain to prepare compound (). The extension of the chain was ex 
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          Sometime ago we have described diamino triazines as histamin2021-11-15  Sometime ago we have described diamino-1,3,5-triazines as histamine H4R ligands,12, 13 and aryl derivatives of the 1,3,5-triazine, which attenuated inflammatory and nociceptive response in vivo in the rodent models of inflammation induced by Protease Inhibitor Cocktail (EDTA-Free, 200X in DMSO) aust 
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          The relationship between the attention deficit hyperactivity2021-11-15  The relationship between the attention deficit hyperactivity disorder (ADHD) and H3Rs is supported by several reports (Berlin et al., 2011; Passani, Bacciottini, Mannaioni, & Blandina, 2000; Vohora & Bhowmik, 2012). ADHD is a neurobehavioral disorder with high prevalence in children, with hyperactiv 
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          A number of in vivo studies2021-11-15  A number of in vivo studies have investigated the antitumor activity of distinct GSK-3 inhibitors in a variety of cancer cell line-derived tumor xenograft models [14], [21], [22], [24], [33], [39], [40]. These studies utilized toolkit GSK-3 inhibitors as monotherapies. Although inhibition of tumor g 
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          caspofungin synthesis br Introduction Atherothrombosis is as2021-11-12  Introduction Atherothrombosis is associated with the presence of a low-grade, subclinical smoldering inflammatory response [1]. Several inflammatory markers, among them high-sensitive C-reactive protein (hs-CRP) [2], the erythrocyte sedimentation rate (ESR) [3], fibrinogen concentrations [4], int 
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          Piezo channels can be activated by many mechanical stimuli W2021-11-12  Piezo channels can be activated by many mechanical stimuli . While some of these stimulations directly mimic physiological forces experienced by CNQX synthesis , such as shear stress applied in a microfluidic chamber, the most commonly used modes of stimulation consist of stretching the membrane b 
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          Therefore as it stands presenilin has a secretase independen2021-11-12  Therefore as it stands, presenilin has a γ-secretase-independent role in regulating protein trafficking, proteolysis and degradation, however given that inhibition of γ-secretase activity can have a negative effect on protein trafficking [69], [98], we cannot exclude the possibility that some of the 
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          br STAR Methods br Introduction Secretase is2021-11-12  STAR★Methods Introduction γ-Secretase is a membrane-embedded proteolytic complex belonging to a diverse family of intramembrane-cleaving proteases and is composed of four integral membrane proteins: presenilin (PS), nicastrin (NCT), anterior pharynx-defective 1 (Aph-1), and presenilin enhancer 
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          br Secretase modulators a loss2021-11-12  γ-Secretase modulators: a loss of pharmacology? A lack of translation from in vitro to in vivo pharmacology is an unresolved issue among most GSMs. R-flurbiprofen was tested in clinical trials, however, it did not achieve statistical significance on either of its primary endpoints – cognition or 
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          br Development of calibrators and controls2021-11-12  Development of calibrators and controls for DiXaIs Method validation and comparison with reference technique (LC:MS) At this stage, anti-Factor Xa bioassays can be established for reliably measuring DiXaI concentrations in plasma, with the available appropriate drug specific calibrators and co 
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          The hyperacetylation of histone proteins2021-11-12  The hyperacetylation of histone proteins by HATs is known to be associated with gene activation [51]. In particular, p300, which is a transcription factor having HAT activity, links activators to the transcription machinery at promoters [52]. The p300/CBP complex dynamically regulates hundreds of di 
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          Conflicting data concerning the involvement2021-11-12  Conflicting data concerning the involvement of H2R on glycaemia has also arisen. Its antagonism was reported to decrease [35], not affect [36], [37] and increase [38], [39] arn-509 receptor levels. In comparison, the clinical experience with antipsychotic drugs generated clearer evidence for the in 
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          There were hub genes identified by WGCNA among which KIBRA2021-11-12  There were 11 hub genes identified by WGCNA among which KIBRA was the hub gene of the black module. The bioinformatics method is an effective and powerful tool to analyze mRNA MK1775 profiles and the related pathways. For instance, the lung cancer risk modules that were closely related to lung canc 
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