加冕 发表于 2025-3-21 18:20:42
书目名称Bile Acids and Their Receptors影响因子(影响力)<br> http://impactfactor.cn/if/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors影响因子(影响力)学科排名<br> http://impactfactor.cn/ifr/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors网络公开度<br> http://impactfactor.cn/at/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors网络公开度学科排名<br> http://impactfactor.cn/atr/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors被引频次<br> http://impactfactor.cn/tc/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors被引频次学科排名<br> http://impactfactor.cn/tcr/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors年度引用<br> http://impactfactor.cn/ii/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors年度引用学科排名<br> http://impactfactor.cn/iir/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors读者反馈<br> http://impactfactor.cn/5y/?ISSN=BK0186220<br><br> <br><br>书目名称Bile Acids and Their Receptors读者反馈学科排名<br> http://impactfactor.cn/5yr/?ISSN=BK0186220<br><br> <br><br>LEER 发表于 2025-3-21 21:00:19
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Structural Insight into the Binding Mode of FXR and GPBAR1 Modulators,resenting promising pharmacological targets. We pay particular attention to the chemical and structural features of the ligand-receptor interaction, providing guidelines to achieve ligands endowed with selective or dual activity towards the receptor and paving the way to future drug design studies.conspicuous 发表于 2025-3-22 06:10:06
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,Pflege der Isolieröle im Betrieb,lectively target GPBAR1 or FXR..In this review, we summarize the most recent acquisition on natural, semisynthetic, and synthetic steroidal and nonsteroidal ligands, able to interact with FXR and GPBAR1.留恋 发表于 2025-3-22 19:58:58
https://doi.org/10.1007/978-3-663-07267-6d their activated receptors in mediating the beneficial metabolic effects of bariatric surgery. We also discuss the potential to target bile acid-activated receptors in order to treat obesity and other metabolic diseases.冷峻 发表于 2025-3-22 23:07:34
The Enterokine Fibroblast Growth Factor 15/19 in Bile Acid Metabolism,he liver. However, native FGF19 seems to retain peculiar hepatic pro-tumorigenic actions. Recently engineered FGF19 analogues have been recently synthetized, with fully retained BA regulatory activity but without intrinsic pro-tumoral action, thus opening bona fide novel pharmacological strategy for the treatment of gut-liver axis diseases.Intend 发表于 2025-3-23 04:34:06
Chemistry and Pharmacology of GPBAR1 and FXR Selective Agonists, Dual Agonists, and Antagonists,lectively target GPBAR1 or FXR..In this review, we summarize the most recent acquisition on natural, semisynthetic, and synthetic steroidal and nonsteroidal ligands, able to interact with FXR and GPBAR1.Gnrh670 发表于 2025-3-23 08:08:18
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