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GPR can signal through not only IP
2022-04-22
GPR40 can signal through not only IP3 but also cAMP depending upon the type of agonist ligand used. A full agonist engages both signaling mechanisms in contrast to the endogenous long-chain fatty bapta am (LCFA) ligands and partial agonists. Thus, stimulation of GPR40 by endogenous LCFAs or by the
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cetp inhibitors br Discussion According to the generally acc
2022-04-21
Discussion According to the generally accepted notion which originated from the study of ATP-depleted cetp inhibitors the changes in Ca2+ homeostasis induced by ATP depletion and leading to the activation of the Gárdos effect are due to the inhibition of Ca2+ pumping, and the subsequent entry of
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KU60019 receptor AD is an irreversible and progressive neuro
2022-04-21
AD is an irreversible and progressive neurodegenerative disease affecting the KU60019 receptor which insidiously destroys memory, thinking skills and cognition. Originally described in 1906 by German physician Alois Alzheimer, AD is characterized by the presence of intraneuronal neurofibrillary tan
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Single cell reverse transcriptase PCR on A mellifera antenna
2022-04-21
Single-cell reverse transcriptase-PCR on A. mellifera antennal lobe (AL) cells showed the expression of RDL as well as another GABA receptor like subunit, LCCH3 (Dupuis et al., 2010). Based on whole cell patch-clamp electrophysiology it was concluded that the predominant GABA receptors in AL cells a
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According to its major function as master regulator
2022-04-21
According to its major function as master regulator of BA homeostasis, FXR has been shown to have a specific tissue distribution; it is expressed along the entire gastrointestinal tract with a peak in the liver and ileum, as well as in the kidney, and adrenal glands [30], [66], [135]. Low FXR expres
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Previous studies have shown that HER is also
2022-04-20
Previous studies have shown that HER2 is also involved in IL-6 expression and signaling. IL-6, HER2, and GP130, the beta-subunit of the IL-6 receptor (IL-6R), are physically associated and co-immunoprecipitate in response to IL-6 stimulation [1]. IL-6 induced HER2 clustering to the GP130 complex, le
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A revolution in cancer immunotherapy has recently emerged wi
2022-04-20
A revolution in cancer immunotherapy has recently emerged with the development of novel immunomodulatory antibodies, classified as immunostimulatory agonist monoclonal 12-O-tetradecanoyl phorbol-13-acetate (mAbs) or checkpoint blocking mAbs. CD40/CD40L, as an important costimulatory pathway, mediat
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One of the key epithelium derived factors required
2022-04-20
One of the key epithelium-derived factors required to maintain immune tolerance in the intestine is Indian Hedgehog (Ihh). Ihh is secreted exclusively by intestinal epithelial cells, and signals in a paracrine manner to the inhibitory receptor Patched1 (Ptch1) on Arctigenin in the mesenchyme. Bind
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Heavy alcohol consumption reported by three of
2022-04-20
Heavy alcohol consumption, reported by three of five referred patients with chronic HCV infection and cirrhosis, is a risk factor for cirrhosis in p.C282Y homozygotes [19], [47] and adults with chronic HCV infection [48]. Although none of the present referred patients were diagnosed to have porphyri
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The initial beta carboline derivatives used in
2022-04-20
The initial beta-carboline derivatives used in the in silico docking experiments were prepared using the procedure outlined in . Harmol, , was -alkylated with -Boc-protected alkylamines in the presence of cesium carbonate to give and . The carbamate protecting group was removed under acidic conditi
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We found that activator drugs
2022-04-20
We found that activator drugs decrease NOsGC protein levels in Sf9 cells. This decrease in protein levels is more pronounced for BAY 60–2770 compared to cinaciguat, and more obvious for α1/β1 compared to α2/β1 (see Fig. 2). This led us to hypothesize that the reduction in protein level correlates wi
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The isoenzyme hGSTP is an attractive drug target
2022-04-20
The isoenzyme hGSTP1-1 is an attractive drug target due to its high levels of disease association (target validation) and druggability (target tractability) properties [5,6,[17], [18], [19], [20], [21]]. hGSTP1-1 functions as a homodimer protein [18]. Each monomer has two domains, an α/β domain (N-t
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br Acknowledgments br Introduction Myelin one of
2022-04-20
Acknowledgments Introduction Myelin, one of the fundamental adaptations of vertebrates, is a multilamellar structure deriving from the spiral wrapping around the SR 2595 of the plasma membrane of myelin forming glia, oligodendrocytes in the central nervous system and Schwann cells (SC) in the
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In addition researchers studying GPR agonists favor
2022-04-20
In addition, researchers studying GPR119 agonists favor the developing of candidate drugs that are more potent than DPP-4 inhibitors given that the latter are moderate agents in the treatment of DM. Although it ion channels is unclear why Sanofi-Aventis chose to terminate collaboration with Metabol
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Strengths The primary feature of GPR
2022-04-20
Strengths The primary feature of GPR119 agonists resides in their dual mechanism of action in regulating blood glucose 1, 2, 3, 15. GPR119 agonists stimulate GLP-1 release from intestinal L RG7388 as well as glucose-dependent insulin secretion and insulin promoter activity enhancement in pancreati
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