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

Intimidate

书目名称3D Cell Culture影响因子(影响力)




书目名称3D Cell Culture影响因子(影响力)学科排名




书目名称3D Cell Culture网络公开度




书目名称3D Cell Culture网络公开度学科排名




书目名称3D Cell Culture被引频次




书目名称3D Cell Culture被引频次学科排名




书目名称3D Cell Culture年度引用




书目名称3D Cell Culture年度引用学科排名




书目名称3D Cell Culture读者反馈




书目名称3D Cell Culture读者反馈学科排名

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

恶心

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