Bio-inspired artificial cilia with magnetic dynamic properties

2015 ◽  
Vol 9 (2) ◽  
pp. 178-184 ◽  
Author(s):  
Leilei Sun ◽  
Yongmei Zheng
2013 ◽  
Vol 25 (7) ◽  
pp. 076004 ◽  
Author(s):  
B Dolgin ◽  
R Puzniak ◽  
D Mogilyansky ◽  
A Wisniewski ◽  
V Markovich ◽  
...  

2013 ◽  
Vol 6 (7) ◽  
pp. 073011 ◽  
Author(s):  
Yuelei Zhao ◽  
Yong Wu ◽  
Yong Jiang ◽  
Liqing Pan ◽  
Young Sun

2019 ◽  
Vol 68 (10) ◽  
pp. 107502
Author(s):  
Qing-Ying Ye ◽  
Wen-Jing Wang ◽  
Chu-Chu Deng ◽  
Shui-Yuan Chen ◽  
Xin-Yuan Zhang ◽  
...  

2018 ◽  
Vol 10 (5) ◽  
pp. 5090-5098 ◽  
Author(s):  
Minghong Tang ◽  
Bingcheng Zhao ◽  
Weihua Zhu ◽  
Zhendong Zhu ◽  
Q. Y. Jin ◽  
...  

2009 ◽  
Vol 9 (2) ◽  
pp. 1635-1639 ◽  
Author(s):  
Qingying Ye ◽  
Qian Feng ◽  
Shuiyuan Chen ◽  
Jianmin Zhang ◽  
Zhigao Huang

2019 ◽  
Vol 473 ◽  
pp. 301-305 ◽  
Author(s):  
Qingying Ye ◽  
Shuiyuan Chen ◽  
Shengkai Huang ◽  
Jinling Wu ◽  
Juyan Xu ◽  
...  

Author(s):  
R.F. Stump ◽  
J.R. Pfeiffer ◽  
JC. Seagrave ◽  
D. Huskisson ◽  
J.M. Oliver

In RBL-2H3 rat basophilic leukemia cells, antigen binding to cell surface IgE-receptor complexes stimulates the release of inflammatory mediators and initiates a series of membrane and cytoskeletal events including a transformation of the cell surface from a microvillous to a lamellar topography. It is likely that dynamic properties of the IgE receptor contribute to the activation of these responses. Fewtrell and Metzger have established that limited crosslinking of IgE-receptor complexes is essential to trigger secretion. In addition, Baird and colleagues have reported that antigen binding causes a rapid immobilization of IgE-receptor complexes, and we have demonstrated an apparent increase with time in the affinity of IgE-receptor complexes for antigen.


2006 ◽  
Vol 73 ◽  
pp. 109-119 ◽  
Author(s):  
Chris Stockdale ◽  
Michael Bruno ◽  
Helder Ferreira ◽  
Elisa Garcia-Wilson ◽  
Nicola Wiechens ◽  
...  

In the 30 years since the discovery of the nucleosome, our picture of it has come into sharp focus. The recent high-resolution structures have provided a wealth of insight into the function of the nucleosome, but they are inherently static. Our current knowledge of how nucleosomes can be reconfigured dynamically is at a much earlier stage. Here, recent advances in the understanding of chromatin structure and dynamics are highlighted. The ways in which different modes of nucleosome reconfiguration are likely to influence each other are discussed, and some of the factors likely to regulate the dynamic properties of nucleosomes are considered.


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