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STRING protein interactions were used to
2020-12-07

STRING protein interactions were used to highlight enzymes directly associated with DHODH (Fig. 10) (Szklarczyk et al., 2015). The reported protein-protein associations are primarily within the de novo nucleotide synthesis pathways (CAD, carbamoyl phosphate synthetase 1, uridine monophosphate synthe
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Substitutions on the benzene ring of the phenyl
2020-12-04

Substitutions on the benzene ring of the phenyl acetic Z-Ligustilide moiety were evaluated to study their effect on DP and CRTH2 selectivity (). Compound has strong affinity for CRTH2, but it only has moderate affinity for DP. Small substitutions such as methoxy () and fluorine () next to the aryl
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br Materials and methods br
2020-12-04

Materials and methods Results and discussion In the present work, we have applied two methodologies, CoMFA and CoMSIA to build 3D-QSAR models. There is no crystal structure available; therefore, an indirect method i.e., a ligand-based approach is the method of choice. The highly active molecul
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However recent studies revealed that the function of Crm mig
2020-12-04

However, recent studies revealed that the function of Crm1 might not only limit to nucleocytoplasmic transport, but also be involved in regulation of centrosome duplication. As the major microtubule organizing centers in animal cells, centrosomes play a significant role in cell cycle, spindle forma
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In this study we observed alterations in
2020-12-04

In this study, we observed alterations in mRNA levels of CRF receptors in the PFCx and Hip during the development of sensitization. In particular, in the Hip both CRF receptors showed significantly increased retinoic acid receptor when the sensitization condition was established. Similarly, CRF2 re
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WRTs AI AI and AI
2020-12-04

WRTs AI-82/1, AI-9-1 and AI-60 showed the same ST as was published by Dingle et al. in RTS 103, 013 and 097 (Dingle et al., 2011). WRTs 015 and 002 were assigned as WRTs 015-like and 002-like due to slight changes in their CE-ribotyping profiles; however, the ST of WRT 002-like (ST8) was identical
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br Materials and methods br Results and discussion
2020-12-04

Materials and methods Results and discussion Conclusions In this study, we have investigated the possibility that hierarchical phosphorylation by CK2 may play a role in cellular signal transduction. Hierarchical phosphorylation by CK2 requires multiple consensus determinants with specific s
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We analyzed whether HaCaT cells
2020-12-04

We analyzed whether HaCaT bcr-abl inhibitor treated with PLD can alter the expression of genes involved in DNA damage response. Key DNA damage cues activate the sensory DNA-PK/ATM/ATR kinases, which relay two parallel cascades that ultimately serve to inactivate the Cyclin B-cdc2 complex. The prote
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In patients with CTEPH ET levels are raised and have
2020-12-04

In patients with CTEPH, ET-1 levels are raised and have been shown to fall after PEA surgery [24]. After an acute pulmonary embolism there is obstruction of the pulmonary ODM-201 receptor by acute thrombus and elevated levels of ET-1 [28], [30]. Elevated levels of ET-1 have also been observed in ai
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br The modulation of ER
2020-12-04

The modulation of ERα: from SERMs to TSECs Continued efforts to provide women with efficacious menopausal therapies have generated interest in the development of selective teniposide sale receptor modulators (SERMs). Similar to estrogens, SERMs have been shown to bind to ERs with high affinity,
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br Disclosure statement br Acknowledgment This
2020-12-04

Disclosure statement Acknowledgment This work was supported by the National Natural Science Foundation of China (81270704, 81330018). Background Over-expression of cyclooxygenase-2 (COX-2) is common in many malignancies including non-small cell lung cancer (NSCLC) and is associated with po
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As illustrated in Table monocyclic acid analogs were synthes
2020-12-04

As illustrated in Table 3, monocyclic ISRIB analogs were synthesized and evaluated. 2-Oxido-3H-1,2,3,5-oxathiadiazol analog 8 showed 15-fold less potent EP1 receptor affinity relative to 2b, while it showed 2.2-fold more potent antagonist activity. Oxadiazole-5-one analog 9 exhibited nearly equipot
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AZD 3965 br Acknowledgements The present study was supported
2020-12-04

Acknowledgements The present study was supported by the Medical Science and Technology Program of Zhejiang Province2014KYA228 (Zhijun Zhou), 2016KYA195 (Jie Li) and 2017KY714 (Qingqing Xia); Zhejiang Provincial Natural Science Foundation of ChinaQ17H120001 (Jie Li); and Scientific Research Projec
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Pleuromutilin australia The development of novel approaches
2020-12-04

The development of novel approaches to study GPCR-mediated transactivation in live Pleuromutilin australia is important, and this study describes a unique BRET-based quantification of Grb2 recruitment to the EGFR as a direct readout of GPCR-mediated transactivation. We have previously used the recr
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Pyruvate dehydrogenase multienzyme complex PDHc catalyzes th
2020-12-03

Pyruvate dehydrogenase multienzyme complex (PDHc) catalyzes the oxidative decarboxylation of pyruvate, and subsequently acetylates coenzyme A (CoA) to acetyl-CoA during the tricarboxylic Tranexamic Acid metabolic pathway using thiamine diphosphate (ThDP) and Mg2+ as cofactors. PDHc poses a key role
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