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br EphB as a therapeutic target in cancer
2020-08-10

EphB4 as a therapeutic target in cancer Eph receptors and ephrins are promising new therapeutic targets in cancer. Various strategies have been employed to evaluate the interference of tumor-promoting effects or the enhancement of tumor suppressive effects. The inhibition of the Eph-ephrin system
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In the present study we investigated the role of
2020-08-10

In the present study, we investigated the role of EP1R after ICH and its mechanism of action. We hypothesized that EP1R activation aggravates ICH injury but that its blockade reduces injury through the Src kinases and the MMP-9 signaling pathway. To test this hypothesis, we examined the effects of s
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ionomycin br Activatable optical imaging probes Optical
2020-08-10

Activatable optical imaging probes Optical fluorescence imaging, which directly detects photons emitted from fluorescent probes, has become as a powerful analytical method to study biological processes both in vitro and in vivo. It is characterized by high sensitivity, is free of radioactive irra
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The Penicillium strain used in this work was isolated
2020-08-10

The Penicillium strain used in this work was isolated from Atlantic forest soil and previously screened as lipase producer (Tauk-Tornisielo et al., 2005). The immobilization was previously evaluated using hydrophobic supports, i.e. agarose based butyl-(But), phenyl-(Phe) and octyl-Sepharose (Oct), a
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Bexarotene sale ACE also known as Kininase II is an
2020-08-10

ACE also known as Kininase II is an important enzyme of the Renin angiotensin Bexarotene sale system (RAAS) (Novo et al., 1987), it is believed to be a potent blood pressure regulator and also plays a crucial role in activation of the bradykinin receptor via inactivation of bradykinin which works to
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Although there is a growing interest in the biological
2020-08-07

Although there is a growing interest in the biological production of xylitol from renewable materials (Albuquerque et al., 2014, Dhar et al., 2016), at present, most of the xylitol is produced on commercial scale by traditional chemical approach that include hydrogenation of pure d-xylose derived fr
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gdc-0980 synthesis In plants SUMOylation has been
2020-08-06

In plants, SUMOylation has been shown to modulate plant hormone signaling (Lois et al., 2003, Miura et al., 2009, Conti et al., 2014), root stem cell maintenance (Xu et al., 2013), and responses to abiotic and biotic stress (Lois, 2010). Many of the plant biological processes regulated by SUMOylatio
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DDR associates with non muscle myosin IIA NMIIA during
2020-08-06

DDR1 associates with non-muscle myosin IIA (NMIIA) during cell migration and spreading on collagen (Huang et al., 2009), but it is not known whether this association is important for DDR1-dependent collagen mechanical remodeling. Here we considered that DDR1 mediates ECM remodeling by focusing cell-
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The US Food and Drug
2020-08-06

The US Food and Drug Administration’s Draft Guidance on Drug Interaction Studies recommends that pharmacokinetic interactions be defined during drug development as part of the drug’s safety and effectiveness. Delafloxacin has been studied in in vitro metabolic studies and is not an inhibitor of cyto
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Based on published reports and our own findings we
2020-08-06

Based on published reports and our own findings, we propose to combine genetic inactivation with pharmacological inhibition in mechanistic studies because the selectivity of many commercially available inhibitors is often limited. Experiments with non-selective inhibitors easily lead to misleading c
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The most interesting findings were the
2020-08-06

The most interesting findings were the observation of differential expression of the NCK and ABI genes between resistant and susceptible hybrid catfish (Fig. 1b). In general, the NCK and ABI genes, with exception of ABI3a gene and NCK1 gene, were expressed at higher levels in susceptible fish after
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br Materials and methods br Results
2020-08-06

Materials and methods Results Discussion In this study, we demonstrated that activation of the EP4 receptor is selectively cytotoxic for malignantly transformed B cells. The effects of the selective EP4 agonist, Pge1-OH, involved inhibition of the NF-κB pathway as well as chemo-sensitizatio
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Introduction Myclobutanil MCL RS chlorophenyl H triazol ylme
2020-08-05

Introduction Myclobutanil (MCL), (RS)-2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile (Fig. 1), is a broad-spectrum systemic triazole fungicide with protective, eradicative, and curative action (University of Hertfordshire, 2018). It is employed to control pests such as powdery mild
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Previous studies have investigated the role of
2020-08-05

Previous studies have investigated the role of norepinephrine in α1-AR, α2-AR and β-AR ontogeny by lesioning the noradrenergic fibers of neonatal rats with 6-hydroxydopamine (6-OHDA). One study found a ∼20% increase in adult α1-AR and α2-AR in cortical membranes (Dausse et al., 1982) and a separate
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The inhibition of the CDKs occurs naturally by INK s
2020-08-05

The inhibition of the CDKs occurs naturally by INK4s and CIPs. Small AZD-5438 australia are being discovered and developed as CDK inhibitors which mainly target ATP binding domain of CDK-cyclin complexes in a reversible and competitive manner or by allosteric inhibition (Fig. 3) [54], [55]. Betzi et
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