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

两边在扩散

书目名称Cell Cycle Oscillators影响因子(影响力)




书目名称Cell Cycle Oscillators影响因子(影响力)学科排名




书目名称Cell Cycle Oscillators网络公开度




书目名称Cell Cycle Oscillators网络公开度学科排名




书目名称Cell Cycle Oscillators被引频次




书目名称Cell Cycle Oscillators被引频次学科排名




书目名称Cell Cycle Oscillators年度引用




书目名称Cell Cycle Oscillators年度引用学科排名




书目名称Cell Cycle Oscillators读者反馈




书目名称Cell Cycle Oscillators读者反馈学科排名

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

山顶可休息

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

他去就结束

恭维

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

健谈