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標(biāo)題: Titlebook: Bioorganic Chemistry of Biological Signal Transduction; Herbert Waldmann Book 2001 Springer-Verlag Berlin Heidelberg 2001 Bioorganic Chemi [打印本頁]

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書目名稱Bioorganic Chemistry of Biological Signal Transduction影響因子(影響力)




書目名稱Bioorganic Chemistry of Biological Signal Transduction影響因子(影響力)學(xué)科排名




書目名稱Bioorganic Chemistry of Biological Signal Transduction網(wǎng)絡(luò)公開度




書目名稱Bioorganic Chemistry of Biological Signal Transduction網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Bioorganic Chemistry of Biological Signal Transduction被引頻次




書目名稱Bioorganic Chemistry of Biological Signal Transduction被引頻次學(xué)科排名




書目名稱Bioorganic Chemistry of Biological Signal Transduction年度引用




書目名稱Bioorganic Chemistry of Biological Signal Transduction年度引用學(xué)科排名




書目名稱Bioorganic Chemistry of Biological Signal Transduction讀者反饋




書目名稱Bioorganic Chemistry of Biological Signal Transduction讀者反饋學(xué)科排名





作者: 不感興趣    時間: 2025-3-21 22:25
Peptidomimetic SH2 Domain Antagonists for Targeting Signal Transduction,lective inhibition of phosphorylating and dephosphorylating enzymes, medicinal chemistry has focused on an SH2 domain-targeted drug design approach. This review will briefly summarize the role of adaptor proteins in signaling networks, followed by an introduction on the functional and structural det
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Ras-Farnesyltransferase-Inhibitors as Promising Anti-Tumor Drugs,alyzed by the enzyme Ras-farnesyltransferase, is essential to its proper functioning in the normal and in the transformed state. Therefore, the inhibition of Ras lipidation has become a promising target for the development of new classes of anti-tumor agents. This review focuses on the different cla
作者: Coterminous    時間: 2025-3-22 12:45
Phosphatidylcholine-Preferring Phospholipase C from ,. Function, Structure, and Mechanism,lar messages are delivered to the cell to induce a response. Of the PLC isoenzymes, the PI-PLCs have perhaps been examined in the greatest detail because of their key role in initiating cellular response by hydrolyzing the phosphodiester bond of phosphatidylinositols and their phosphorylated derivat
作者: 先行    時間: 2025-3-22 13:20
Photoaffinity Labeling in Biological Signal Transduction,accelerates the development of new selective medicines. The determination of the disease related molecular targets is also essential in these efforts. Photoaffinity labeling provides a well-established technique for identification, localization of binding proteins, and studying intracellular protein
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https://doi.org/10.1007/3-540-45035-1Bioorganic Chemistry; Bioorganische Chemie; Biophysics; Biophysik; DNA; Signal Transduction; Signal-Transd
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Herbert WaldmannThis series presents critical reviews of the present position and future trends in modern chemical research.Short and concise reports on chemistry, each written by the world renowned experts.Still val
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https://doi.org/10.1007/978-3-662-03253-4lective inhibition of phosphorylating and dephosphorylating enzymes, medicinal chemistry has focused on an SH2 domain-targeted drug design approach. This review will briefly summarize the role of adaptor proteins in signaling networks, followed by an introduction on the functional and structural det
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https://doi.org/10.1007/978-3-662-03253-4accelerates the development of new selective medicines. The determination of the disease related molecular targets is also essential in these efforts. Photoaffinity labeling provides a well-established technique for identification, localization of binding proteins, and studying intracellular protein
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Modelling of Pulsed-Laser Ablationa putative model for mammalian PC-PLCs. The similarity of the active site of PLC. with other phosphoryl transfer enzymes has also served as a stimulus for mechanistic studies. The present account details recent studies of this important member of the PLC superfamily of enzymes.
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作者: 該得    時間: 2025-3-25 20:09
Bioorganic Chemistry of Biological Signal Transduction
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作者: 重疊    時間: 2025-3-26 18:44
https://doi.org/10.1007/978-3-662-03253-4of the iterative optimization cycles revealing new peptidomimetic and non-peptide SH2 domain antagonists. Finally, an outlook is given on further applications of the modular chemistry concept and the privileged building blocks, that have been developed in SH2 domain inhibitor programs, onto a new class of adaptor proteins, notably the PTB domains.
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