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br Acknowledgements br Introduction Pregnancy brings forth
2022-01-03
Acknowledgements Introduction Pregnancy brings forth significant metabolic reprogramming that induces a number of metabolic changes to ensure that the nutrient requirements of the mother and fetus are met [[1], [2], [3]]. These adaptations change radically over the period of pregnancy dependin
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s equol br Heme and the HO system Heme a complex of
2022-01-03
Heme and the HO system Heme, a complex of iron and protoporphyrin IX, has versatile functions, which are critical for the survival of all aerobic organisms including mammalians and bacteria [9]. The central iron in heme facilitates six ligand binding sites [10], four of which are occupied by nitr
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The endocytic inhibitors MDC and CPZ and dynamin GTPase
2022-01-03
The endocytic inhibitors MDC and CPZ and dynamin GTPase blocker (dynamin mutant) have been shown to significantly decrease the intracellular accumulation of cGMP. Moreover, earlier reports suggested that G-protein-coupled receptor (GPCRs) continue to signal by generating cAMP throughout internalizat
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K-Ras(G12C) inhibitor 12 sale br Introduction Soluble guanyl
2022-01-03
Introduction Soluble guanylyl cyclase (GC-1) maintains vascular function through the NO/GC-1/cGMP pathway [1,2] by catalyzing the conversion of GTP into cGMP (Fig. 1). The GC-1 heme prosthetic group binds NO with picomolar affinity, resulting in a 100- to 200-fold increase in catalytic activity.
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As a result of the capability of modulating the
2022-01-03
As a result of the capability of modulating the dynamic changes and rearrangement of cytoskeletons, the Rho GTPases, in which RhoA, Cdc42 and Rac1 are best-characterized, have been highlighted as significant contributors for orchestrating neuronal development (Duman et al., 2015, Heasman and Ridley,
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porcine mg Decreasing GSK activity has therapeutic benefits
2022-01-03
Decreasing GSK-3β activity has therapeutic benefits in animal model of colitis [45] and traumatic porcine mg injury [46] and ischemia/reperfusion injury [47,48]. In brain, activation of GSK-3β promotes Aβ toxicity by elevating APP expression and its amyloidogenic cleavage, and by dysregulating Aβ c
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Then the seven complexes GLOI indomethacin GLOI zomepirac GL
2022-01-03
Then the seven complexes (GLOI-indomethacin, GLOI-zomepirac, GLOI-fenoprofen, and GLOI-ketoprofen, GLOI-tolmetin GLOI-curcumin, and GLOI-bisdemethoxycurcumin) were energy-minimized to remove unfavorable steric strain relative to the force field adopted. Further MD simulations were carried out based
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The transport of glutamate by EAAT from the extracellular fl
2022-01-03
The transport of glutamate by EAAT2 from the extracellular fluid into either astrocytes or endothelial cells is an unfavorable and energy-consuming process. This energy is provided by a coupled co-transport of three sodium ions, one proton, and one glutamate molecule in the counter-transport of one
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We report on four affected children from
2022-01-03
We report on four affected children from two unrelated consanguineous additional hints with moderate to severe ID associated with epilepsy and variable neuropsychiatric features. Using whole-exome sequencing, we identified homozygous missense variants in SLC45A1 (OMIM: 605763), which codes for a neu
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Given the estimated number of NSVDC channels in a
2022-01-03
Given the estimated number of 150–300 NSVDC channels in a red cell [7] and a single channel conductance of 30 pS at physiological salt concentrations [6], the maximum conductance observed in intact red Scrambled 10Panx receptor indicate either a very low open state probability, in the order of 10−3
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mpges-1 inhibitors Piezo channels can be activated
2022-01-03
Piezo channels can be activated by many mechanical stimuli . While some of these stimulations directly mimic physiological forces experienced by mpges-1 inhibitors , such as shear stress applied in a microfluidic chamber, the most commonly used modes of stimulation consist of stretching the membra
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br Conclusion and future directions GS is an important thera
2022-01-03
Conclusion and future directions GS is an important therapeutic target for the treatment of Alzheimer's disease. Its structure and function have been studied during the last years to understand the substrate cleavage mechanism to modulate the Aβ42 peptide production. The recent elucidation of GS
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Comparison of dlGALRs deduced amino
2022-01-03
Comparison of dlGALRs deduced amino gpr44 inhibitor sequences with that of human GALRs demonstrate that the GALR1 ortholog sequences have diverged less than those of GALR2. Since often duplicate genes undergo divergent evolution through sub-functionalization, loss or gain of new functions (Prince a
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Knock out mice of FXR showed enhancing
2022-01-03
Knock-out mice of FXR showed enhancing cholesterol metabolism in vivo and reducing serum levels of total cholesterol. Additionally, the results of FXR-deficiency mice revealed potential effects on the improvement of obesity and diabetes.19, 20 As a natural FXR ligand, guggulsterone possesses antagon
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br Acknowledgments We apologize to
2022-01-03
Acknowledgments We apologize to the researchers who were not referenced due to space limitations. We thank Christine Heiner (Department of Surgery, University of Pittsburgh) for her critical reading of the manuscript. This work was supported by grants from the US National Institutes of Health (R0
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