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Beyond phosphorylation cancer cells may alter pyrimidine
2021-08-09
Beyond phosphorylation, cancer SP 141 may alter pyrimidine biosynthesis through the activation of the proto-oncogenic transcription factor MYC. MYC is a master regulator of many different pathways and has significant influence on the expression of nucleotide metabolism genes. Previous studies have s
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A number of studies have been carried out to
2021-08-09
A number of studies have been carried out to understand lipid production pathways and to increase TAGs level in higher plants. Overexpression of key melanin of the Kennedy pathway until now is by far the most successful strategy to increase TAG lipid content in Brassica napus, Arabidopsis thaliana
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br Results and discussion To check the hypothesis that the
2021-08-09
Results and discussion To check the IKK-16 hydrochloride australia that the charge of α-synuclein can be altered due to the glycation, we measured zeta potential of native α-synuclein and α-synuclein glycated by two different glycating agents, methylglyoxal (MG) and glyceraldehyde-3-phosphate (G
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Apoptozole synthesis Collectively the results presented here
2021-08-09
Collectively, the results presented here provide new insights into ligand binding, clustering, spatial distribution, and phosphorylation of DDR1b and DDR2 in response to soluble collagen I. As depicted in the cartoon of Scheme 1, we postulate a model in which the spatial distribution and assembly of
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ampar The CPA EoS was presented by Kontogeorgis et
2021-08-09
The CPA EoS was presented by Kontogeorgis et al., in 1996 [23]. The proposed equation is composed of two parts (SRK EOS + association term) such that it can well predict the thermodynamic behavior of hydrogen bonding materials as a result of considering the association term. Yakoumis et al. (1997) e
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For the first time we provide evidence
2021-08-09
For the first time, we provide evidence for COMT Val158Met modulation of long-term fear extinction in humans, evident both in cortical (LPP) and autonomic (fear bradycardia) components of the conditioned fear response. We further found that the initial acquisition of fear is related to dispositional
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From an industrial perspective the low turnover numbers and
2021-08-06
From an industrial perspective, the low turnover numbers and limited substrate scope of α-KG halogenases still represents a significant challenge. However, in light of the fact that currently no chemical processes are available for the selective halogenation of aliphatic carbon centers in complex mo
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CAA is a carcinogenic metabolite of vinyl chloride forming s
2021-08-06
CAA is a carcinogenic metabolite of vinyl chloride, forming several different DNA adducts including the cyclic dihydrofolate reductase inhibitor antibacterial adducts 3,N4-ethenocytosine (εC), 1,N6-ethenoadenine (εA), N2,3-ethenoguanine (εG), and 1,N2-ethenoguanine (1,N2-εG), with the A and C cycli
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Herein we explored by docking studies the effectiveness of r
2021-08-06
Herein, we explored by docking studies the effectiveness of replacing the dimethyl substitution at C (6) of dihydrotriazine with a folded azaspiro-containing substituent, along with the introduction of differently substituted phenyl- and benzyl-rings or alkyl chains, linked at the position 1 of the
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Given the excellent in vitro pharmacology profiles of methyl
2021-08-06
Given the excellent in vitro pharmacology profiles of methyl ester 28 and primary amide 29 efforts were reengaged on neutral analogs of these leads, with a focus on non-amide replacements for the carboxylic MK 0893 functionality of 1. Acetonitrile 49 was found to have a good balance of DGAT-1 inhib
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Finally our results suggest that R may
2021-08-06
Finally, our results suggest that σ2R may, at least partially, mediate the hunger-suppressive action of amphetamine by interacting with orexigenic receptors in CRF2R-OX1R heteromer contexts. Despite extensive evidence supporting the formation of GPCR oligomers in heterologous systems, the lack of ap
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In the preclinical evaluation of CRF receptor antagonists
2021-08-06
In the preclinical evaluation of CRF1 receptor antagonists, effects were mainly focused on the regulation of hyperactivated HPA axis and the modulation of anxiety or depressive-like behaviors in CRF challenge [16], [17], [18] or stress models [16], [19], [20]. However, it remains to be concluded whe
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The present findings suggested that nsEP inhibited CPG
2021-08-06
The present findings suggested that nsEP inhibited CPG2 via deprivation of zinc ions, with no effect on apoenzyme integrity. Zinc may be removed from CPG2 by the electric forces. Within CPG2, each zinc ion was coordinated by one histidine, one glutamate and one aspartate [6]. The nsEP field can alte
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Due to its several industrial applications the recombinant p
2021-08-05
Due to its several industrial applications, the recombinant production of collagen and all its derivatives as gelatins has been pursued for many years in different biological systems as mammalian nebivolol hcl (Toman et al., 1999), tobacco plants (Ruggiero et al., 2000), silkworms (Tomita et al., 20
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Introduction br CK in the
2021-08-05
Introduction CK1 in the Regulation of Hh Pathway CK1 was initially identified as a negative regulator of Hh signaling at the level of transcription factor Ci by genetic studies in Drosophila and genome-wide RNAi screen in Drosophila cultured Spautin-1 (Jia et al., 2005, Lum et al., 2003, Price
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