Enzyme Activities in Biopsy Specimens from Large-Bowel Mucosa in Colorectal Adenomas and Carcinomas

1987 ◽  
Vol 22 (5) ◽  
pp. 533-538 ◽  
Author(s):  
B. Børkje ◽  
O. D. Lærum ◽  
E. Schrumpf
1987 ◽  
Vol 42 (1) ◽  
pp. 56-60 ◽  
Author(s):  
Lemuel Herrera-Ornelas ◽  
Carl Porter ◽  
Paula Pera ◽  
William Greco ◽  
Nicholas J. Petrelli ◽  
...  

1998 ◽  
Vol 184 (2) ◽  
pp. 153-160 ◽  
Author(s):  
Sukhdev Singh ◽  
Richard Poulsom ◽  
Andrew M. Hanby ◽  
Len A. Rogers ◽  
Nicholas A. Wright ◽  
...  

1979 ◽  
Vol 57 (2) ◽  
pp. 181-185 ◽  
Author(s):  
B. T. Cooper ◽  
D. C. A. Candy ◽  
J. T. Harries ◽  
T. J. Peters

1. Jejunal biopsy specimens from three children with congenital sucrase—isomaltase deficiency were assayed for disaccharidase activity and were subjected to analytical subcellular fractionation with enzymic microanalysis. 2. By use of the highly sensitive fluorigenic modification of the disaccharidase assay, brush-border sucrase and isomaltase activities were depressed but nevertheless detectable in each child. 3. Apart from the expected decrease in brush-border α-glucosidase activity, the other enterocyte marker-enzyme activities were normal. 4. There were no abnormalities in the enterocytes of any child on analytical subcellular fractionation or on electron microscopy.


Pathology ◽  
2020 ◽  
Vol 52 ◽  
pp. S95
Author(s):  
Laura Wise ◽  
Dakshesh Vakil ◽  
Marjorie Walker ◽  
Ella Sugo
Keyword(s):  

1990 ◽  
Vol 30 (1-2) ◽  
pp. 264-266 ◽  
Author(s):  
R. Mennigen ◽  
J. Kusche ◽  
C. Streffer ◽  
B. Krakamp

1986 ◽  
Vol 21 (9) ◽  
pp. 1051-1057 ◽  
Author(s):  
B. Børkje ◽  
S. Ødegaard ◽  
D. W. Skagen ◽  
K.-J. Andersen ◽  
E. Schrumpf

2004 ◽  
Vol 4 (3) ◽  
pp. 24-30 ◽  
Author(s):  
Svjetlana Radović ◽  
Ivan Selak ◽  
Mirsad Babić ◽  
Zora Vukobrat-Bijedić ◽  
Željka Knežević

The aim of this paper is to establish by immunohistochemistry the expression of keratin 7 in inflammatory-regenerative flat bowel mucosa and in different grades of epithelial dysplasia regarding the sub-units expressed in normal and carcinomatous colonic mucosa. Biopsy specimens from 270 patients were examined: 74 were classified as inflammatory-regenerative changes and 196 as dysplastic lesions. There were 108 cases of mild dysplasia, 58 cases of moderate and 30 cases of severe dysplasia, respectively). Demonstration of location and intensity of cytokeratin 7 staining was performed by immunohistochemistry using monoclonal antibody (anti-cytokeratin 7). Findings of cytokeratin 7 in dysplastic lesions were compared with those in normal mucosa, inflammatory -regenerative mucosa and adenocarcinoma. Cytokeratin 7 is not found in normal colonic mucosa. In inflammatory-regenerative mucosa it was found in solitary cells in small number of cases. It is found in all cases of epithelial dysplasia and its expression showed no difference regarding moderate and severe dysplasia. In few cases of adenocarcinoma, cytokeratin 7 is found in traces and showed minimal staining intensity. Having in mind that cytokeratine 7 is primarily found in dysplastic lesions of the flat colonic mucosa it can be a valuable diagnostic tool in the histological interpretation of epithelial dysplasia.


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