Titlebook: Cell Cycle Oscillators; Methods and Protocol Amanda S. Coutts,Louise Weston Book 2021Latest edition Springer Science+Business Media, LLC, p

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書目名稱Cell Cycle Oscillators影響因子(影響力)




書目名稱Cell Cycle Oscillators影響因子(影響力)學(xué)科排名




書目名稱Cell Cycle Oscillators網(wǎng)絡(luò)公開度




書目名稱Cell Cycle Oscillators網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Cell Cycle Oscillators被引頻次




書目名稱Cell Cycle Oscillators被引頻次學(xué)科排名




書目名稱Cell Cycle Oscillators年度引用




書目名稱Cell Cycle Oscillators年度引用學(xué)科排名




書目名稱Cell Cycle Oscillators讀者反饋




書目名稱Cell Cycle Oscillators讀者反饋學(xué)科排名

aspect

Anhydrous

https://doi.org/10.1007/978-94-6209-622-6llators comprising of protein kinases and their regulators. Different cell cycle oscillators are inextricably linked to ensure orderly activation of oscillators. A recurring theme in their regulation is the abundance of autoamplifying loops that ensure switch-like and unidirectional cell cycle trans

Organization

Origins: A Sustainable Concept in Educationn-dependent kinases (Cdks) and other cell cycle kinases. Here, I present the rationale and the experimental framework for an alternative approach to measure kinase activity that is based on estimating substrate phosphorylation rates in vivo. The approach presented was first developed for experiments

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Fred Dervin,Hanna Ragnarsdóttirthe APC/C targets its two essential substrates, securin and cyclin B, for proteasomal destruction. Cyclin B is the activator of cyclin-dependent kinase 1 (Cdk1), the major mitotic kinase, and both cyclin B and securin are safeguards of sister chromatid cohesion. Conversely, the degradation of securi

Pudendal-Nerve

https://doi.org/10.1007/978-94-6209-854-1ission. A wide variety of genetically-encoded and synthetic biosensors have been developed to monitor protein kinase activity. We have focused on the design, engineering and characterization of fluorescent peptide biosensors of cyclin-dependent kinases (CDKs) that constitute attractive cancer biomar

Pudendal-Nerve

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On the Facilitation of the Academypression of mRNA expression. However, full-length 3′UTR vectors are rarely employed due to labor-intensive cloning work. Instead, 3′UTR fragments containing putative miRNA binding sites are commonly utilized to mechanistically validate miRNAs. Assaying truncated 3′UTRs may falsely validate miRNAs du

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