Basic Studies on High Pressure Air Plasmas

2006 ◽  
Author(s):  
Karl H. Schoenbach
2000 ◽  
Author(s):  
Igor Adamovich ◽  
J. Rich ◽  
Andrey Chernukho ◽  
Serguei Zhdanok

2007 ◽  
Vol 101 (9) ◽  
pp. 093302 ◽  
Author(s):  
K. Frederickson ◽  
W. Lee ◽  
P. Palm ◽  
I. V. Adamovich ◽  
J. W. Rich ◽  
...  

Author(s):  
Kraig Frederickson ◽  
Wonchul Lee ◽  
Igor Adamovich ◽  
J. Rich ◽  
Walter Lempert ◽  
...  

2001 ◽  
Author(s):  
Peter Palm ◽  
Elke Plonjes ◽  
Igor Adamovich ◽  
Vish Subramaniam ◽  
Walter Lempert ◽  
...  

2012 ◽  
Vol 45 (45) ◽  
pp. 455203 ◽  
Author(s):  
B Peyrou ◽  
L Chemartin ◽  
Ph Lalande ◽  
B G Chéron ◽  
Ph Rivière ◽  
...  

2001 ◽  
Author(s):  
Igor Adamovich ◽  
J. Rich ◽  
Peter Palm ◽  
Elke Plonjes ◽  
Matt Buoni ◽  
...  

Author(s):  
Marek Malecki ◽  
James Pawley ◽  
Hans Ris

The ultrastructure of cells suspended in physiological fluids or cell culture media can only be studied if the living processes are stopped while the cells remain in suspension. Attachment of living cells to carrier surfaces to facilitate further processing for electron microscopy produces a rapid reorganization of cell structure eradicating most traces of the structures present when the cells were in suspension. The structure of cells in suspension can be immobilized by either chemical fixation or, much faster, by rapid freezing (cryo-immobilization). The fixation speed is particularly important in studies of cell surface reorganization over time. High pressure freezing provides conditions where specimens up to 500μm thick can be frozen in milliseconds without ice crystal damage. This volume is sufficient for cells to remain in suspension until frozen. However, special procedures are needed to assure that the unattached cells are not lost during subsequent processing for LVSEM or HVEM using freeze-substitution or freeze drying. We recently developed such a procedure.


Author(s):  
Robert Corbett ◽  
Delbert E. Philpott ◽  
Sam Black

Observation of subtle or early signs of change in spaceflight induced alterations on living systems require precise methods of sampling. In-flight analysis would be preferable but constraints of time, equipment, personnel and cost dictate the necessity for prolonged storage before retrieval. Because of this, various tissues have been stored in fixatives and combinations of fixatives and observed at various time intervals. High pressure and the effect of buffer alone have also been tried.Of the various tissues embedded, muscle, cartilage and liver, liver has been the most extensively studied because it contains large numbers of organelles common to all tissues (Fig. 1).


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