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Titlebook: Web 2.0; Jens Behrendt,Klaus Zeppenfeld Textbook 2008 Springer-Verlag Berlin Heidelberg 2008 AJAX.Internet.RSS.Semantic Web.Web.Web 2.0.We

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21#
發(fā)表于 2025-3-25 06:31:53 | 只看該作者
22#
發(fā)表于 2025-3-25 10:57:34 | 只看該作者
ming more and more utilized.Includes state-of-the-art views G protein-coupled receptors (GPCRs) are heptahelical transmembrane receptors that convert extra-cellular stimuli into intra-cellular signaling, and ultimately into biological responses. Since GPCRs are natural targets for approximately 40%
23#
發(fā)表于 2025-3-25 14:27:30 | 只看該作者
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發(fā)表于 2025-3-25 16:10:32 | 只看該作者
25#
發(fā)表于 2025-3-25 20:57:19 | 只看該作者
imarily through a positive control exerted by the pituitary hormone thyroid stimulating hormone (TSH) and a negative control exerted by iodine. In most physiological circumstances the maintenance of eumetabolism requires steady concentrations of circulating thyroid hormones. This is achieved by a cl
26#
發(fā)表于 2025-3-26 01:55:04 | 只看該作者
27#
發(fā)表于 2025-3-26 07:17:22 | 只看該作者
Even more recent methodological developments, like in situ hybridization of receptor mRNA, provide excellent localization of receptor gene expression, but also give little information about receptor coupling to intracellular signaling mechanisms. In order to address this question, techniques must be
28#
發(fā)表于 2025-3-26 10:14:25 | 只看該作者
accelerated by at least two different types of guanosine triphosphatase (GTPase) activating protein (GAP) complexes: RGS11/Gβ5/R9AP and RGS7/Gβ5/GPR179. A third complex may contain RGS11/Gβ5/GPR179. Certain elements of these GAP complexes (RGS7 and RGS11) are redundant, but others (Gβ5 and GPR179) a
29#
發(fā)表于 2025-3-26 15:29:02 | 只看該作者
30#
發(fā)表于 2025-3-26 16:47:25 | 只看該作者
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