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Since the interaction between the E
2020-08-04
Since the interaction between the E2 and E3 is weak and transient, it has been difficult to identify novel interactions between specific E2/E3 complexes [59], [64]. Here we used a modified bait consisting of the Mulan RING domain fused to one of the four E2s isolated in our screen and expressed in y
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The chemical structure of curcusone D is different
2020-08-04
The chemical structure of curcusone D is different from all of the reported DUB inhibitors. It contains cross-conjugated α, β-unsaturated ketones (Fig. 1A). A similar pharmacophore was previously described in the pan-DUB inhibitor prostaglandin lipid derivatives, which function as potent Michael rec
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As noted by the authors a limitation
2020-08-03
As noted by the authors, a limitation of this study is that alternative activation of CPT1a-deficient macrophages was only assessed in vitro. An important question is how macrophage-specific CPT1a-deficient mice behave in vivo in situations like asthma, helminth infections, wound healing, and tumors
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Ramipril synthesis br Introduction The cyclin dependent kina
2020-08-03
Introduction The cyclin-dependent kinase 1 (Cdk1) associated with cyclin B plays a central role in M phase of the mitotic Ramipril synthesis (Enserink and Kolodner, 2010). The meiotic cell cycle consists of two successive divisions, meiosis I and meiosis II, which are also driven by cyclin B-Cdk
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The analysis of progression from autoantibody positivity to
2020-08-03
The analysis of progression from autoantibody positivity to clinical disease is in essence measuring the rate of this progression as long-term follow-up results indicate that close to all of the children testing positive for two or more autoantibodies progress to clinical disease within 15–20 years
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The closed configuration is secured by interactions involvin
2020-08-03
The closed configuration is secured by interactions involving multiple distal MCC elements 48, 51. First, the IR tail from the CDC20M of MCC docks in the vacant TPR groove from the second APC8 molecule in APC/C. Second, the BUBR1 subunit of MCC hijacks the UBE2C-binding surface on the WHB subdomain
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A major advance was made in the endothelin field with
2020-08-03
A major advance was made in the endothelin field with the development of endothelin Compound C antagonists. In particular, BQ-123 (cyclo (d-Trp–d-Asp–Pro–d-Val–Leu)) (Ihara et al., 1991) and FR139317 ((R)2-[(R)-2-[(S)-2-[[1-(hexahydro-1H-azepinyl)]carbonyl]amino-4-+++methylpentanoyl] amino-3-[3-(1-m
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Amphiphilic compounds lower interfacial tension and its
2020-08-03
Amphiphilic compounds lower interfacial tension and its biological production often results in a competitive environmental advantage (Darvishi et al., 2011). The reduction of interfacial tension can increase the biologically available surface areas resulting in increased AZD-5438 of insoluble compo
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br STAR Methods br Author Contributions Z Z
2020-08-03
STAR★Methods Author Contributions Z.Z., H.G., and C.Y. conceived the project. C.Y. performed almost all experiments. H.G. performed all bioinformatics and statistical analysis. H.G. and J.H. performed some of the experiments. S.D. performed the in vitro DNA replication experiments under the gu
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The pharmacodynamic potential of compound was initially eval
2020-08-03
The pharmacodynamic potential of Isorhamnetin 52 was initially evaluated in an oral triglyceride tolerance test. C57BL/6 mice were treated with vehicle, 0.1, 0.3 or 1mg/kg of 52 30min prior to dosing with a corn oil bolus. Plasma triglyceride (TG) levels were monitored every hour over the course of
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Egr together with catecholamine biosynthetic enzymes
2020-07-31
Egr1, together with catecholamine biosynthetic enzymes, such as tyrosine hydroxylase (TH), dopamine β-hydroxylase (DBH), and phenylethanolamine N-methyltransferase (PNMT), is induced in adrenal medulla by different types of stress (Liu et al., 2005, Morita et al., 1996, Nankova et al., 1993, Papanik
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Acknowledgments The authors thank Pierre Alain Bayle
2020-07-31
Acknowledgments The authors thank Pierre-Alain Bayle for his contribution in the recording of NMR data and Colette Lebrun for ESI-MS spectrum. This research was supported by the Labex ARCANE (Grant ANR-11-LABX-0003-01). Introduction The activation of oncogenes during tumorigenesis generates DNA
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fty720 br Conflicts of interest br
2020-07-31
Conflicts of interest Grant support Natural Science Foundation of China (81302862). Introduction Over 50 years ago the great biochemist Otto Warburg proposed that oxygen fty720 was a key factor in cancer induction. Indeed, experimental evidence that mutagenic and toxic DNA lesions are gene
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We finally examined whether N BMAA is cytotoxic to
2020-07-31
We finally examined whether N-BMAA is cytotoxic to SH-SY5Y cells. SH-SY5Y is an immortalised neuroblastoma cell line with many of the characteristics of neuronal cells. It is used commonly for investigations of BMAA induced neuronal toxicity and in other studies relating to AD, ALS, and ALS/PDC (Lop
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Resistance to SP is linked to
2020-07-31
Resistance to SP is linked to point mutations that accumulate at several sites in the dihydrofolate reductase (dhfr) and dihydropteroate synthase (dhps) Fmoc-Tyr(tBu)-OH of P. falciparum (Roper et al., 2003). These mutations have been identified in codons 16, 51, 59, 108, and 164 in the dhfr gene an
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