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GLP is an intestinal peptide hormone
2022-01-19
GLP-1 is an intestinal peptide hormone that is released by the gut following ingestion of food, particularly Darunavir Ethanolate receptor and fats. Following its release, GLP-1 stimulates pancreatic β-cells to secrete insulin (Hirasawa et al., 2005, Covington et al., 2006). Originally, GLP-1 acted
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We noticed that the spontaneous openings of the
2022-01-19
We noticed that the spontaneous openings of the D97R α1 GlyR appeared to be quite similar to those elicited by a maximally-effective glycine concentration on wildtype GlyR; both generated similar open and shut dwell-time histograms, both exhibited openings grouped into clusters with Popen values gre
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br Results and Discussion br STAR Methods br Author
2022-01-19
Results and Discussion STAR★Methods Author Contributions Conflicts of Interest J.P.F. is a consultant for AstraZeneca, BMS, Johnson and Johnson, Novo Nordisk, and Sanofi, a member of the advisory panel for AstraZeneca and Sanofi, a member of the speaker’s bureau for Sanofi and Novo Nordi
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Immunohistochemistry analysis shown ghrelin and GHSR a immun
2022-01-19
Immunohistochemistry analysis shown ghrelin and GHSR-1a immunostaining was located in the epithelial cells of rociletinib synthesis and ducts throughout the lactation, strong immunoreactive cells were detected in L30, L60 and L120 stage. The distribution of ghrelin has been shown in many tissues, i
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glucagon receptor In fact changes in mitochondrial dynamics
2022-01-19
In fact, changes in mitochondrial dynamics directly affects many things including cellular metabolism [127], mitochondrial mass and turnover [128], mitochondrial transport, and calcium buffering [129]. Nigrostriatal DA neurons seem to have a preferential susceptibility to loss of Mfn2 when compared
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br Voltage dependent anion channel VDAC is
2022-01-19
Voltage-dependent anion channel VDAC is a ubiquitous protein showing well conserved structural and functional properties in spite of major variations in its sequence (for review see [50]). Most of what we know about VDAC electrophysiological properties (for reviews, see [51], [52]) was initially
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The release of FBPase and aldolase from subcellular
2022-01-19
The release of FBPase and aldolase from subcellular structures of muscle was dependent on the presence of the crowding agent imitating the physiological conditions – PEG 8000 (Table 1). The amount of both enzymes associated with structures of muscle chembridge was about 6–7 times higher in the pres
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Recent advances in imaging single protein
2022-01-19
Recent advances in imaging single protein mobility and organization in live organisms such as Drosophila larva motor nerve terminals have initiated this by providing a useful platform to investigate how the dynamic changes in the actomyosin network correlates with vesicle docking and fusion in vivo2
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Sperm exocytosis or acrosome reaction AR is
2022-01-19
Sperm exocytosis or acrosome reaction (AR) is a regulated secretion with special characteristics essential for fertilization. The AR relies on the same highly conserved molecules that drive intracellular membrane fusion and exocytosis in all other UM 171 (see [59] for a recent review). Two such mol
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P Benzoxaborole substituted macrocyclic compounds based on I
2022-01-18
P4-Benzoxaborole-substituted macrocyclic compounds based on ITMN-191 scaffold were prepared using a general scheme as shown in . ITMN-191 was prepared by following a patent procedure. The P4 BOC group was removed by treatment with TFA in dichloromethane to give amine . The coupling of the amine to 6
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To date very little is known
2022-01-18
To date, very little is known about the GEFs that regulate RhoA during amoeboid migration. GEF-H1, a RhoA GEF, is activated response to microtubule destabilization and promotes amoeboid migration (Eitaki, Yamamori, Meike, Yasui, & Inanami, 2012). Interestingly, the majority of HL 2448 depleted of a
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We have previously established the pharmacokinetic profile a
2022-01-18
We have previously established the pharmacokinetic profile and effective dose of MNF in the rat [43] and demonstrated the effectiveness of MNF as an anticancer drug in jak stat pathway and xenograft models [44]. Moreover, MNF was found to effectively block GPR55 signaling in tumor cells [21]. The co
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br Material and methods br Results br Discussion Organisms
2022-01-18
Material and methods Results Discussion Organisms have developed a variety of anti-glycation defense mechanisms. In SU6656 sale to the aldose-reductase-pathway or 2-oxoaldehyde dehydrogenase-pathway, the glyoxalase system is the only mechanism, which is not restricted to liver [19]. This sy
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The study of TcMYH protein is
2022-01-18
The study of TcMYH protein is a step forward for the characterization of a GO system in T. cruzi. The complete system appears to be present and our findings demonstrate that is important to maintain DNA stability of the nuclear and mitochondrial genomes, particularly in the presence of oxidative str
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br Declaration of interest br Acknowledgments
2022-01-18
Declaration of interest Acknowledgments This work was supported by grants from the Polish National Science Centre (PRELUDIUM grant no. 2013/11/N/NZ5/00270) and the European Commission FP7 Project Beta-JUDO (grant number 279 153), European Union EIT Health project DeTecT2D, Swedish Diabetes A
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