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DDR kinases are linked to
2020-07-30
DDR kinases are linked to the progression of various human diseases, including fibrotic disorders, atherosclerosis and cancer [9], [12], [13]. Significantly, they are identified as indicators of poor prognosis in ovarian, breast and lung cancer [14], [15], [16]. DDR1 overexpression is associated wit
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They located EAI with vast efficiency and selectivity
2020-07-30
They located EAI001 with vast efficiency and selectivity for mutant EGFR (at 1 mM ATP, IC50 0.024 μM for L858R T790M, IC50 > 50 μM for wild-type EGFR) as EGFR allosteric inhibitor-1. However, it best had modest potency towards individual L858R and T790M mutants. After medicinal-chemistry-based enhan
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In an effort to discover additional GPCRs directing the migr
2020-07-30
In an effort to discover additional GPCRs directing the migratory events of responding B cells, we identified Epstein-Barr virus (EBV)-induced gene 2 (EBI2) as a promising candidate. The gene encoding EBI2 (Ebi2, also known as Gpr183) was originally identified together with Ebi1 (Ccr7) as the most h
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br RINGs as activators of E
2020-07-30
RINGs as activators of E2~Ub In LY3039478 to HECT-type E3 ligases, RING-type E3s lack a bona fide catalytic center. A lingering question in the field has been whether RINGs serve solely to position E2~Ub relative to the substrate, or if they also serve as activators of E2~Ub. Clearly, unwanted ub
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In the case of high fidelity polymerases we propose that
2020-07-30
In the case of high-fidelity polymerases, we propose that water is used to achieve negative selection against nucleotide binding. With specialized DNA polymerases, we propose that nucleobase desolvation plays a different yet important role in allowing these enzymes to replicate damaged DNA. In this
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The present work together with our
2020-07-30
The present work, together with our previous study, offers a means of conferring collagen-binding integrin-, VWF- and DDR-reactivity upon an inert substrate. GPRGQOGVNleGFO is known to bind not only VWF and DDR2, but also DDR1 and SPARC (Secreted Protein Acidic and Rich in Cysteine) [20,52]. We ther
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DDRs a novel subfamily of receptor
2020-07-30
DDRs, a novel subfamily of receptor tyrosine kinases, were discovered during the search for tyrosine kinase proteins expressed in human malignancies 5, 6. DDRs can modulate cell responses such as adhesion, migration, differentiation, survival and proliferation, in response to the changes in the amou
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Kuo et al Have shown that DAPK
2020-07-30
Kuo et al. (2006) Have shown that DAPK1 function in inhibiting microtubule (MT) assembly is through the activation of microtubule affinity-regulating kinases (MARK)/PAR-1 family kinases MARK1/2, which destabilize MT by phosphorylating tau and related MAP2/4. This relation with DAPK1 has demonstrated
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Both CysLT and CysLT receptors are expressed in the gastroin
2020-07-30
Both CysLT1 and CysLT2 receptors are expressed in the gastrointestinal system. CysLT1 receptors are expressed in the small intestine, colon and liver, whereas CysLT2 receptors are found in the stomach, small intestine, colon, liver and pancreas (Brink et al., 2003, Kanaoka and Boyce, 2004, Capra et
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Cancer cells promote low grade inflammatory conditions in th
2020-07-30
Cancer Valinomycin promote low-grade inflammatory conditions in the surrounding milieu to support tumorigenesis [1]. The tumor micro-environment is influenced also via exosomes, nanovesicles which can be released by all cell types including cancer cells and immune cells, and carry RNA, proteins and
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Fumonisin B1 synthesis The X ray crystal structure of riboci
2020-07-30
The X-ray crystal structure of ribociclib bound to CDK6 shows that the N3 of the pyridine fragment hydrogen bonds with the NH group of V101 (the third hinge residue) and the adjacent amino group NH hydrogen bonds with the V101 carbonyl group (Fig. 7C). The drug carbonyl oxygen hydrogen bonds with th
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The present results were unanticipated based on
2020-07-30
The present results were unanticipated based on the majority of data in the literature. Instead of blocking the behavioral and biochemical correlates of anxiety, we found a significant, and in the case of ASV-30, dose-dependent, potentiation by CRF2 receptor antagonists of fear-stimulated rat freezi
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In the present study we investigated whether FSH
2020-07-30
In the present study, we investigated whether FSH and bFGF are able to regulate molecular mechanisms involved in FA metabolism and in mitochondrial biogenesis. In addition, in the case that FA metabolism and mitochondrial biogenesis are regulated by FSH and bFGF, if PPARβ/δ activation has any role i
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br Results and discussion br Conclusions The
2020-07-30
Results and discussion Conclusions The results of KKR and KKR-CPA electronic structure calculations were presented for LiMO2 compounds and LiNiCoMn0.1O2 solid solutions, respectively. It was found that Mn impurity located in semiconducting LiCoO2 matrix might exhibit magnetic moment. The mixin
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Several limitations of this study should be noted First
2020-07-30
Several limitations of this study should be noted. First, like all candidate gene association studies (Ebstein et al., 2012), the sample size of this study was relatively small, particularly for the male group. As women in general report lower well-being than men (Pinquart and Sörensen, 2001), we ex
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