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br EBI An Endogenous TM Receptor Manipulated by
2020-08-07

EBI2: An Endogenous 7TM Receptor Manipulated by EBV EBI2 was identified in 1993, when Kieff and colleagues used subtractive hybridization of DNA from Burkitt\'s lymphoma cells to screen for upregulated genes in EBV-infected cells. They found, being more than 200-fold upregulated (hence the name:
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Until recently the first line treatment of RLS
2020-08-07

Until recently, the first line treatment of RLS was the administration of low dose of three dopaminergic drugs, which has been approved by the US Food and Drug Administration and the European Medicines Agency for the treatment of moderate to severe RLS. These compounds are pramipexole (Mirapex), rop
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The in vitro studies support our previous
2020-08-06

The in vitro studies support our previous observations of a bimodal expression pattern of B. malayi transcripts after tetracycline treatment, including the two enzymes we studied here. We hypothesize that this bimodal expression may be due to stage-specific responses of the host in response to Wolba
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Introduction Eicosanoid lipid prostaglandin D PGD is the maj
2020-08-06

Introduction Eicosanoid lipid prostaglandin D2 (PGD2) is the major prostaglandin produced by activated mast AI-10-49 (Lewis and Austen, 1981). The physiological function of PGD2 is mainly mediated by two G protein-coupled receptors (GPCRs), PGD2 receptor 1 and 2 (DP1 and DP2), which share modest s
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br Material and methods br Results br Discussion This study
2020-08-06

Material and methods Results Discussion This study was performed to investigate the molecular correlates of addiction in a model based on the development of psychomotor sensitization which takes place after repeated nicotine administrations (Carboni et al., 2016; Vezina et al., 2007; Zivian
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Researches aforementioned provide effective numerical theore
2020-08-06

Researches aforementioned provide effective numerical/theoretical descriptions of expansion behavior of PELE when small-caliber projectiles penetrating thin target at high impact velocity. Here we presented a similar study on large-caliber PELE projectile (130 mm) with various thickness steel jacket
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A generally applicable strategy to
2020-08-06

A generally applicable strategy to screen for improved α-KGD activity could be based on the generation of succinate by the decarboxylation of α-KG [49]. In this context, Escherichia coli strains were engineered, in which succinate-producing enzymes from the TCA (3S,5S)-Atorvastatin sodium salt austr
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br Acknowledgements br Introduction Botulinum neurotoxin BoN
2020-08-05

Acknowledgements Introduction Botulinum neurotoxin (BoNT) is a uniquely potent protein synthesized by Clostridium botulinum, C. baratii and C. butyricum, (Rosetto et al., 2014, Kukreja and Singh, 2014). It acts on cholinergic nerve endings and blocks the release of Ristocetin A sulfate synthes
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Using the juxtarenal PPE the
2020-08-05

Using the juxtarenal PPE, the induction of juxta- and suprarenal aneurysms is described herein (Fig. 3A). The infra-/suprarenal part of the Roxithromycin sale can now be investigated separately, taking into account different embryological backgrounds and varying reactivity to differing stimuli (revi
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br Acknowledgements This work was aided
2020-08-05

Acknowledgements This work was aided by discussions with R. Hietpas, P. Mishra, L. Jiang, C. R. Matthews, R. Gilmore, and P. Pryciak. We are grateful for assistance from the University of Massachusetts Medical School Core Flow Cytometry Laboratory and R. Konz with cell sorting experiments. This w
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The sulfonamide was important for the DP
2020-08-05

The sulfonamide was important for the DP activity: no potent dual antagonists were identified through the modification of this functional group. Multiple modifications of the phenylacetic Phusion high-fidelity DNA polymerase sale moiety have been reported, such as bioisoteric replacements of the car
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eicosapentaenoic acid In conclusion HTS identified the
2020-08-05

In conclusion, HTS identified the pyrazole-4-acetic eicosapentaenoic acid substructure as a micromolar hit. The SAR of the scaffold was investigated, showing significant differences in some case to the SAR of reported indole acetic acid CRTh2 antagonists. SAR was able to identify as a very potent
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TTP 22 By using a cohort of
2020-08-05

By using a cohort of clinical SRCT cases with previously confirmed fusion events, ChildSeq-RNA correctly identified gene fusions in 15 of 16 ES samples, all six aRMS samples, the two DSRCT samples, and one CFS sample. The single failed ES case (which also failed in an RT-PCR experiment that we perfo
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ERR is constitutively active in the absence of endogenous
2020-08-05

ERRγ is constitutively active in the absence of endogenous ligand. However, several synthetic ligands that can repress or induce ERRγ function by disrupting ERRγ-coactivator interactions have been reported to date. The estrogen receptor modulators diethylstilbestrol (DES) and 4-hydroxytamoxifen (4-O
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br Discussion We described dually targeting CRBN
2020-08-05

Discussion We described dually targeting CRBN-VHL PROTACs, developed with the aim of investigating the relative ability of CRBN and VHL E3 ligase to induce degradation of one other. Among the three series of compounds developed, we observed preferential degradation of one ligase i.e. CRBN over th
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