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CYP s are heme containing
2020-12-08

CYP450s are heme-containing monooxygenases constituting a conserved gene superfamily of heme-thiolate proteins, and are found in prokaryotes and eukaryotes (Martignoni et al., 2006). They play a key role in detoxification of endogenous (e.g., steroids) and exogenous compounds (e.g., drug, insecticid
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br Conclusions The present study demonstrated that CuE posse
2020-12-08

Conclusions The present study demonstrated that CuE possesses strong hepatotoxicity. CuE is not only a mechanism-based inhibitor of human CYP3A4, but also inhibits P-gp activity in vitro. In whole animal studies, CuE induces CYP3A and P-gp after a long-term treatment but inhibits the activities o
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TCS 5861528 br Data deposition The structure factor
2020-12-08

Data deposition: The structure factor amplitudes and coordinates of mIL34 and the mIL-34:mCSF-1R complex have been deposited in the Protein Data Bank, www.pdb.org, with accession codes 4EXN and 4EXP. Note added in proof The authors would like to inform the readers of two recent articles that are
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Common to all models for nuclear transport is the binding
2020-12-08

Common to all models for nuclear transport is the binding of importins/exportins to FG repeats found in about a third of the ∼30 nucleoporins, the so-called FG-Nups (Iovine et al., 1995, Rexach and Blobel, 1995); for review, see Grossman et al. (2012), Stewart (2007), and Terry and Wente (2009). FG-
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The question remained as to why hCrm was functional and
2020-12-08

The question remained as to why hCrm1 was functional and mCrm1 was not in terms of Rev and HIV mRNA nuclear export, and previously we proposed three possibilities (Elinav et al., 2012). One was that human TPEN had a positively acting factor that somehow stabilized the hCrm1 and Rev-RRE complex (but
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Under optimized assay conditions very low concentrations
2020-12-08

Under optimized assay conditions, very low concentrations (20pM) of [125I]YP20 bound to hCRF1-CHO BB-94 receptor membranes with high specificity (>95% inhibited by 1μM astressin) and in a membrane protein-dependent manner. Specific binding was selective vs. the hCRF2α subtype because little specifi
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AMPK is a master regulator
2020-12-08

AMPK is a master regulator of metabolic homeostasis, its broad spectrum of metabolic activities makes it an attractive target for treatment of metabolic and related disorders including Diabetes and Obesity (Madhavi et al., 2018). It controls lipid metabolism through its target genes PPAR-γ, C/EBP-α
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Early studies from the mollusk Aplysia reported the presence
2020-12-08

Early studies from the mollusk, Aplysia, reported the presence of a unique class of Radotinib receptors in neurons, the acetylcholine-gated chloride channels (ACCs) (Kehoe and McIntosh, 1998). Later, studies identified these receptors in the model nematode Caenorhabditis elegans (Putrenko et al., 2
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Over the last decade numerous studies have evaluated
2020-12-07

Over the last decade, numerous studies have evaluated the acute, short-term, and medium-term impact of pulmonary vasodilators on Fontan physiology.23., 24., 25., 26., 27., 28., 29., 30., 31. Although different JP 1302 dihydrochloride of medications have been evaluated, phosphodiesterase-5 (PDE-5) i
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Synthetic progestogens also known as
2020-12-07

Synthetic progestogens (also known as ‘synthetic gestagens’, ‘synthetic progestins’ or simply ‘progestins’) are designed to mimic the effects of progesterone (P4) and are the active pharmaceutical ingredient in many contraceptives and hormone replacement therapies. Since most progestins are derived
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br Physiological roles for EPAC isoforms vascular function T
2020-12-07

Physiological roles for EPAC isoforms: vascular function The effects of cAMP on limiting vascular endothelial cell (VEC) inflammation and vascular smooth muscle cell (VSMC) proliferation have been well documented 36, 37, 38. However, recent work has demonstrated that several key effects of cAMP i
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br Introduction Our understanding of how ligands interact wi
2020-12-07

Introduction Our understanding of how ligands interact with G protein coupled receptors is evolving, particularly the recognition that some have the ability to preferentially activate a subset of intracellular signalling cascades – so called pathway biased ligands [1]. Additionally, it is now acc
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br Acknowledgements The present study was supported by
2020-12-07

Acknowledgements The present study was supported by the Medical Science and Technology Program of Zhejiang Province2014KYA228 (Zhijun Zhou), 2016KYA195 (Jie Li) and 2017KY714 (Qingqing Xia); Zhejiang Provincial Natural Science Foundation of ChinaQ17H120001 (Jie Li); and Scientific Research Projec
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Although CCR expression clearly identifies MBC precursors wi
2020-12-07

Although CCR6 expression clearly identifies MBC precursors within the GC, we found that the expression of this chemokine receptor by responding lrrk2 was not required for MBC differentiation and had no detectable impact on the GC subsets analyzed in this study. Although this is in agreement with st
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Each of these substrate receptors belongs to
2020-12-07

Each of these substrate receptors belongs to a multigene family with tens, if not hundreds of members in plants, and with in part overlapping and in part differential substrate specificities [4]. The complexity of the system is nicely illustrated by the F-box protein and auxin receptor TRANSPORT INH
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