New Experimental Model Design for Vapex Process Experiments

Author(s):  
A. Yazdani J. ◽  
B.B. Maini
AIAA Journal ◽  
2019 ◽  
Vol 57 (4) ◽  
pp. 1715-1724 ◽  
Author(s):  
Liu Lei ◽  
Dai Guangyue ◽  
Zeng Lei ◽  
Wang Zhenfeng ◽  
Gui Yewei

1994 ◽  
Vol 13 (2) ◽  
pp. 91-96 ◽  
Author(s):  
Gamal M. Ghoniem ◽  
Todd L. Vandenberg

2015 ◽  
Vol 26 (6) ◽  
pp. e467-e471 ◽  
Author(s):  
Yingfang Fan ◽  
Jae Hoon Jeong ◽  
Ga Young You ◽  
Ji Ung Park ◽  
Tae Hyun Choi ◽  
...  

2019 ◽  
Vol 10 (40) ◽  
pp. 5473-5486
Author(s):  
Nieves Iglesias ◽  
Elsa Galbis ◽  
Lucía Romero-Azogil ◽  
Elena Benito ◽  
M.-Jesús Díaz-Blanco ◽  
...  

The experimental model design proposed herein has proved to be an indispensable tool to rapidly and easily elucidate the optimal polymerization conditions in the preparation of tailor-made responsive materials for biomedical applications.


Author(s):  
Waykin Nopanitaya ◽  
Raeford E. Brown ◽  
Joe W. Grisham ◽  
Johnny L. Carson

Mammalian endothelial cells lining hepatic sinusoids have been found to be widely fenestrated. Previous SEM studies (1,2) have noted two general size catagories of fenestrations; large fenestrae were distributed randomly while the small type occurred in groups. These investigations also reported that large fenestrae were more numerous and larger in the endothelial cells at the afferent ends of sinusoids or around the portal areas, whereas small fenestrae were more numerous around the centrilobular portion of the hepatic lobule. It has been further suggested that under some physiologic conditions small fenestrae could fuse and subsequently become the large type, but this is, as yet, unproven.We have used a reproducible experimental model of hypoxia to study the ultrastructural alterations in sinusoidal endothelial fenestrations in order to investigate the origin of occurrence of large fenestrae.


2003 ◽  
Vol 2 (1) ◽  
pp. 33-34
Author(s):  
B SHIVALKAR ◽  
B MEURIS ◽  
R VANBENEDEN ◽  
J KETESLEGERS ◽  
F BECKERS ◽  
...  

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