Hildebrand Reynolds, Bonnie. Space, Time and Crisis: The Theatre of René Marqués. York, South Carolina: Spanish Literature Publishing Company. 1988Hildebrand Reynolds, Bonnie. Space, Time and Crisis: The Theatre of René Marqués. York, South Carolina: Spanish Literature Publishing Company. 1988. Pp. 120.

1990 ◽  
Vol 46 (3) ◽  
pp. 568-570
Author(s):  
Maria del C. Cerezo
Keyword(s):  
South Carolina ◽  
Spanish Literature ◽  
Space Time ◽  
Publishing Company

scholarly journals Space-time variation of respiratory cancers in South Carolina: a flexible multivariate mixture modeling approach to risk estimation

2017 ◽  
Vol 27 (1) ◽  
pp. 42-51 ◽  
Author(s):  
Rachel Carroll ◽  
Andrew B. Lawson ◽  
Russell S. Kirby ◽  
Christel Faes ◽  
Mehreteab Aregay ◽  
...  
Keyword(s):  
South Carolina ◽  
Time Variation ◽  
Risk Estimation ◽  
Mixture Modeling ◽  
Space Time ◽  
Modeling Approach ◽  
Mixture Modeling Approach

Recent Scholarship in Spanish Literature

1968 ◽  
Vol 21 (1) ◽  
pp. 118-124
Author(s):  
Alexander A. Parker
Keyword(s):  
Spanish Literature ◽  
Recent Scholarship

An Ultrastructural Comparison of Hepatocytes from ADH+ and ADH−Peromyscus Maniculatus

1996 ◽  
Vol 54 ◽  
pp. 30-31
Author(s):  
J. T. Ellzey ◽  
D. Borunda ◽  
B. P. Stewart
Keyword(s):  
South Carolina ◽  
Adult Male ◽  
Uranyl Acetate ◽  
Model System ◽  
Deer Mice ◽  
En Bloc ◽  
Genetic Stock ◽  
Hepes Buffer ◽  
Transmission Electron ◽  
Color Scanner

Genetically alcohol deficient deer mice (ADHN/ADHN) (obtained from the Peromyscus Genetic Stock Center, Univ. of South Carolina) lack hepatic cytosolic alcohol dehydrogenase. In order to determine if these deer mice would provide a model system for an ultrastructural study of the effects of ethanol on hepatocyte organelles, 75 micrographs of ADH+ adult male deer mice (n=5) were compared with 75 micrographs of ADH− adult male deer mice (n=5). A morphometric analysis of mitochondrial and peroxisomal parameters was undertaken.The livers were perfused with 0.1M HEPES buffer followed by 0.25% glutaraldehyde and 2% sucrose in 0.1M HEPES buffer (4C), removed, weighed and fixed by immersion in 2.5% glutaraldehyde in 0.1M HEPES buffer, pH 7.4, followed by a 3,3’ diaminobenzidine (DAB) incubation, postfixation with 2% OsO4, en bloc staining with 1% uranyl acetate in 0.025M maleate-NaOH buffer, dehydrated, embedded in Poly/Bed 812-BDMA epon resin, sectioned and poststained with uranyl acetate and lead citrate. Photographs were taken on a Zeiss EM-10 transmission electron microscope, scanned with a Howtek personal color scanner, analyzed with OPTIMAS 4.02 software on a Gateway2000 4DX2-66V personal computer and stored in Excel 4.0.

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