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Bioinformatic analysis revealed a putative
2022-01-11

Bioinformatic analysis revealed a putative coiled-coil SLD within CT229 which we show to be essential for intracellular replication and recruitment of Rab GTPases to the inclusion. Mutation of a single amino btz calculator residue in the SLD domain (CT229L120D) significantly reduced Rab binding and
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AEE788 Chronic exposure of cells to cytotoxic drugs can resu
2022-01-11

Chronic exposure of cells to cytotoxic drugs can result in the selection of multiple phenotypic and genetic changes. Thus, the use of MCF7/VP cells, which were selected for resistance to VP-16, was potentially problematic. However, a thorough characterization of MCF7/VP cells demonstrated that they
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br GSNOR regulates SA synthesis and SA signalling The phenol
2022-01-11

GSNOR1 regulates SA synthesis and SA signalling The phenolic metabolite salicylic Protease Inhibitor Cocktail (EDTA-Free, 100X in DMSO) (SA) is a powerful immune activator in plants. Moreover, mutations that disable SA biosynthesis or transgenes that result in its depletion compromise both resis
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LY3009120 Several investigators including ourselves have pre
2022-01-11

Several investigators including ourselves have previously shown, that allogeneic HLA-DPB1 class II-alleles are powerful leukemia rejection LY3009120 for CD4 T-cell therapy following allogeneic hematopoietic stem cell transplantation (Herr et al., 2017, Rutten et al., 2008, Stevanovic et al., 2012)
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br Conclusions The results of
2022-01-10

Conclusions The results of this work showed that β-glucosidase could be efficiently immobilized onto hydroxyapatite nanoparticles in a single adsorption step. The enzyme adsorption was accomplished by coordination bonds between remaining Ca2+ sites of HA and COO− of amino acids. The immobilizatio
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br Conclusions Temporally controlled disruption
2022-01-10

Conclusions Temporally-controlled disruption of Gcgr reveals a lack meaningful contribution to the improvement of glycemic control in insulinopenic conditions attributable to the intrinsic loss of GCGR signaling. On the other hand, these data highlight the importance of compensatory systems, incl
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Ulimorelin also known as TPZ is a macrocyclic molecule that
2022-01-10

Ulimorelin, also known as TPZ101, is a macrocyclic molecule that is a potent agonist of the ghrelin receptor (Hoveyda et al., 2011). Due to its ability to stimulate gastrointestinal motility, ulimorelin has been evaluated as a possible treatment in gastroparesis (Ejskjaer et al., 2010), ileus (Frase
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Until recently the mechanism of
2022-01-10

Until recently the mechanism of how GSMs shifted γ-secretase cleavage was poorly understood. Today, building on the sequential cleavage model developed by Ihara and colleagues [14], there is evidence that GSMs act as processivity enhancers, and iGSMs as inhibitors of processivity [120]. At least for
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br Methods br Results It is well
2022-01-10

Methods Results It is well known that during the onset of vasoconstriction there is an increase in intracellular Ca2+ which activates myosin light-chain kinase followed by cycling of actin-myosin cross-bridges in VSMCs. Recently, it has been recognized that BML-210 polymerization is also invol
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Nitidine chloride mg Our results are consistent with the hyp
2022-01-10

Our results are consistent with the hypothesis that reduced Fas-mediated apoptosis in maternally activated T-lymphocytes could result in insufficient trophoblast invasion of the spiral Nitidine chloride mg as the activated T-lymphocytes become able to enhance the destruction of the cytotrophoblasts
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Several other assay parameters were also explored First
2022-01-10

Several other assay parameters were also explored. First, the thermal dependence of the assay was investigated by measuring the specific activity at different temperatures (Fig. 7). That data show that enzymatic activity increases with increasing temperature. Interestingly, the observed rate increas
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T0901317 australia A second site of histone
2022-01-10

A second site of histone core domain acetylation that that has been observed on newly synthesized histones is histone H4 lysine 91 [34]. H4 lysine 91 lies along the interface between the H3/H4 tetramer and the H2A/H2B dimers. In fact, H4 lysine 91 normally forms a salt bridge with an aspartic T09013
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br Results br Discussion The present
2022-01-10

Results Discussion The present findings outline a novel regulatory mechanism for fasting-induced ketogenesis, which involves histamine release from mast c-myc inhibitor into the hepatic portal system, H1 receptor-mediated stimulation of liver OEA biosynthesis, and recruitment of the nuclear r
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br Structural studies of GCAP Recoverin was the first member
2022-01-10

Structural studies of GCAP Recoverin was the first member of this subfamily of Ca2+-binding ck1 inhibitor to be investigated by structural methods [27], [54], [55], [56], [57], [58]. These proteins have four EF-hands arranged in pairs that give rise to amino- and carboxyl-terminal domains. The c
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The opposite modulation observed for circulating LPI levels
2022-01-10

The opposite modulation observed for circulating LPI levels and WAT GPR55 Piroxicam by nutritional status suggests that increased levels of LPI may down-regulate the expression of its receptor in WAT, whereas in conditions of low serum LPI levels, the expression of GPR55 is stimulated. However, dur
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