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What are the in situ effects
2023-09-28

What are the in-situ effects of multi-site CaM associations with AT1R? Kai et al. showed that synthetic peptides corresponding to residues 125–137 (rat sequence) in SMD2, 217–227 in the N-terminal side of SMD3, and 304–316 in SMD4JM inhibit to various degrees AngII-induced GTPase activity of isolate
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br Androgen interference with the
2023-09-28

Androgen interference with the action of arachidonic transcription factors metabolites’ actions; the other side of the coin Arachidonic acid, being a polyunsaturated fatty acid present in the phospholipids of the membrane of cells, is highly abundant within the organism. It is mainly involved in
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The current results also demonstrated tendencies toward
2023-09-28

The current results also demonstrated tendencies toward decreased serum Aβ40 levels and increased Aβ42 levels during the 1-year follow-up. These tendencies are consistent with the results of a previous study that evaluated Aβs in the CSF of patients with late-life depression (Pomara et al., 2016).
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APP is a member of a conserved protein family
2023-09-28

APP is a member of a conserved protein family that also includes amyloid precursor-like proteins 1 and 2 (APLP1, APLP2).8, 9, 10 The proteins in this family are type I single-pass transmembrane procollagen c proteinase with receptor-like structural features but not entirely clear cellular functions
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Here we provide evidence that NO contributes to
2023-09-28

Here, we provide evidence that NO contributes to changes in synaptic strength, but also offer an explanation as to why previous attempts to link NO to LTP have often failed. Our results describe a model by which cycling AMPARs, held in intracellular pools, are rapidly delivered to the membrane surfa
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Calmidazolium chloride australia br The lipoxygenase pathway
2023-09-28

The 12/15-lipoxygenase pathway in diseases of the nervous system Conclusions and future perspectives Arachidonic Calmidazolium chloride australia and other polyunsaturated fatty acids, and their lipid metabolites, play very important roles in human health and disease. This review has outlined
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Lorlatinib is an orally active brain penetrant cyclic aminop
2023-09-28

Lorlatinib is an orally active brain penetrant cyclic 2-aminopyridine derivative that is a type I½ B ALK inhibitor (Fig. 5F) [61]. This medicinal is an effective antagonist against the more common L1196M and G1269A crizotinib-resistant mutations as well as the less common T1151Ins, L1152R, C1156Y, F
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Various compounds have been designed to inhibit
2023-09-28

Various compounds have been designed to inhibit aldose reductase (AR) [12]. These compounds can be classified into two main categories, the first category comprises those containing a carboxylic met inhibitor moiety, for example, 3-thiazolidineacetic acid derivative, which has been reported to be a
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Growing evidence indicates that GRKs can
2023-09-28

Growing evidence indicates that GRKs can exert different effects within the cell depending on the stimulus, cell type, and localization [97], [121]. In this sense, we were the first to demonstrate a mitochondrial localization for GRK2 [122], later confirmed by other investigators [123], establishing
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Our findings establish a critical link between HemAC Lm dime
2023-09-28

Our findings establish a critical link between HemAC-Lm dimeric structure and cAMP synthesis that helps in explaining how globin-A domain influences AC domain. The following possible homodimeric structure of wild type full length HemAC-Lm has been proposed to explain the role of this globin-A domain
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AMPK modulates changes in lipid metabolism via the regulatio
2023-09-28

AMPK modulates changes in lipid metabolism via the regulation of fatty gamma-Secretase inhibitor IX oxidation and cholesterol synthesis in the liver. The key enzymes involved include ACC and HMGCR [27,28]. Both participate in the rate-limiting steps of fatty acids and cholesterol synthesis and are
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The H N mutation in exon has
2023-09-27

The H373N mutation in exon 6 has not previously been reported [3], [4], [5], [6]; thus, this mutation appears to be a novel mutation. The functional expression study demonstrated that the H373N mutation results in almost complete loss of enzymatic activity. Thus, it is highly likely that the H373N m
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Aurora A overexpression is also related to
2023-09-27

Aurora-A overexpression is also related to the activation of NF-κB, a potent anti-apoptotic effector that may play a role in preventing apoptosis in cancer CC-223 mg [18]. These data show that we are still at the beginning of unraveling the complex mechanism by which these gene products and protei
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Zhang et al screened three
2023-09-27

Zhang et al. screened three thousand compounds library and found two active 3,5,6-substituted indolin-2-one molecules. Further, they designed various derivatives of this scaffold and among them compound 23 from the series was found active with 1.8 μM on Aurora-B kinase luminescent assay [53]. Jeffe
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Placental cells also express P aromatase CYP A encoded by
2023-09-27

Placental cells also express P450 aromatase (CYP19A1, encoded by CYP19A1). In the placenta, this enzyme requires an external source of androgens, provided by the adrenal gland of the fetus, to form estrogen. The fetal adrenal gland produces dehydroepiandrosterone (DHEA) [9] and, in the placenta, it
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