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Titlebook: Drug Development; Molecular Targets fo Timothy S. Gaginella,Antonio Guglietta Book 2000 Springer Science+Business Media New York 2000 cytok

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發(fā)表于 2025-3-21 17:28:56 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱Drug Development
副標(biāo)題Molecular Targets fo
編輯Timothy S. Gaginella,Antonio Guglietta
視頻videohttp://file.papertrans.cn/284/283062/283062.mp4
圖書(shū)封面Titlebook: Drug Development; Molecular Targets fo Timothy S. Gaginella,Antonio Guglietta Book 2000 Springer Science+Business Media New York 2000 cytok
描述The application of molecular techniques to gastroenterology continues to yield important advances in the development of drugs to treat gastrointestinal disorders. Important new drugs have emerged through the collaborative and complementary efforts of basic scientists, clinicians, and clinical researchers in academia and the pharmaceutical industry. The challenge has been exciting, with a few surprises along the way. Consider peptic ulcer disease as an example. The discovery of H receptors and the availability of potent and 2 selective H-receptor antagonists signaled the beginning of a new era 2 in the treatment of gastric hypersecretory states and peptic ulcers. Introduction of proton pump inhibitors offered another therapeutic option. Though H-receptor antagonists and proton pump inhibitors 2 are important and useful drugs, the discovery of the link between H. pylori infection and peptic ulcer disease has led to even more effective pharmacotherapeutic regimens. Our intent in Drug Development: Molecular Targets for GI Diseases is to bring together hands-on experts to review promising areas of gastrointestinal pharmacology. The contemporary topics covered, from a mechanistic viewpoi
出版日期Book 2000
關(guān)鍵詞cytokine; development; drug; drug development; drugs; inflammation; liver; liver disease; opioid; peptides; ph
版次1
doihttps://doi.org/10.1007/978-1-59259-202-9
isbn_softcover978-1-61737-087-8
isbn_ebook978-1-59259-202-9
copyrightSpringer Science+Business Media New York 2000
The information of publication is updating

書(shū)目名稱Drug Development影響因子(影響力)




書(shū)目名稱Drug Development影響因子(影響力)學(xué)科排名




書(shū)目名稱Drug Development網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱Drug Development網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱Drug Development被引頻次




書(shū)目名稱Drug Development被引頻次學(xué)科排名




書(shū)目名稱Drug Development年度引用




書(shū)目名稱Drug Development年度引用學(xué)科排名




書(shū)目名稱Drug Development讀者反饋




書(shū)目名稱Drug Development讀者反饋學(xué)科排名




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Opioid Receptors, the most used analgesics. Besides a predominant role in pain control (both somatic and visceral pain), opioids and opioid receptors have a broad spectrum of actions, including modulations of reinforcement and reward pathways, neurotransmitter release, neuroendocrine functions, as well as gastrointe
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Ute Winkels,Yoko Schlütermann-Sugiyama. In this chapter, the biological actions of the eicosanoids are reviewed, as are the enzymes through which they are formed, and the receptors through which they act. The potential of drugs that block the activity of these enzymes or the eicosanoid receptors is reviewed, particularly with respect to
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Ute Winkels,Yoko Schlütermann-Sugiyamadies on the role of NO in the GI tract, especially as it relates to maintenance of physiological function and mucosal integrity; the therapeutic potential of agents that modulate the NO system will also be discussed.
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