Titlebook: 3D Cell Culture; Methods and Protocol Zuzana Koledova Book 2017 Springer Science+Business Media LLC 2017 Hydrogels.3D Organoids.Scaffolds.O

Intimidate

書目名稱3D Cell Culture影響因子(影響力)




書目名稱3D Cell Culture影響因子(影響力)學(xué)科排名




書目名稱3D Cell Culture網(wǎng)絡(luò)公開度




書目名稱3D Cell Culture網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱3D Cell Culture被引頻次




書目名稱3D Cell Culture被引頻次學(xué)科排名




書目名稱3D Cell Culture年度引用




書目名稱3D Cell Culture年度引用學(xué)科排名




書目名稱3D Cell Culture讀者反饋




書目名稱3D Cell Culture讀者反饋學(xué)科排名

Temporal-Lobe

Methods in Molecular Biologyhttp://image.papertrans.cn/012/image/100701.jpg

Ige326

https://doi.org/10.1007/978-1-4939-7021-6Hydrogels; 3D Organoids; Scaffolds; Organotypic cultures; Micropatterning; Microfluidics; Bioprinting; Thre

arboretum

978-1-4939-8370-4Springer Science+Business Media LLC 2017

惡心

ECG769

https://doi.org/10.1007/978-3-322-83139-2–cell and cell–extracellular matrix interactions, 3D cell culture enables proper structural architecture and differentiated function of normal tissues or tumors in vitro. Thereby 3D cell culture realistically models in vivo tissue conditions and processes, and provides in vivo like responses. Since

Hallmark

https://doi.org/10.1007/978-3-322-83139-2bserved in vivo. Decellularization of tissues and organs has been shown to be an effective method for the removal of potentially immunogenic constituents while preserving essential growth factors and extracellular matrix (ECM) proteins necessary for proper cell function. Enzymatic digestion of decel

hegemony

https://doi.org/10.1007/978-3-322-83244-3 with native extracellular matrix (ECM) proteins, nonnative biopolymers, or synthetic polymers are often used to study these processes in vitro in 3D cell culture experiments. However, each of these materials systems present major limitations when used in mechanobiological studies. While native ECM-

Nonconformist

https://doi.org/10.1007/978-3-322-83244-3of advanced three dimensional (3D) culture models. Herein, we report methods for the PEG-GAG gel-based 3D co-cultivation of human umbilical vein endothelial cells, mesenchymal stromal cells, and different cancer cell lines. The resulting constructs allow for the exploration of interactions between s

negligence

https://doi.org/10.1007/978-3-322-83253-5sical cell reprogramming process. Surprisingly, the contribution of the three-dimensional (3D) microenvironment to iPSC generation has been largely overlooked. Here we describe a protocol for the generation of iPSCs in defined poly(ethylene glycol) (PEG)-based hydrogels that, besides allowing higher