Expression of cyclin a in intestinal biopsies from children with celiac disease.
In conclusion, these studies enabled us visualized pattern of distribution of cyclin A but let us also to presume that observed decrease of expression and its distribution might function as additional factor which could be taken under consideration to establish terminal diagnosis. We are aware of the fact that these are very first observations and that this subject needs to be further investigated with the use of additional methods and samples. Key words: celiac disease, cyclin A, immunogold, immunohistochemistry.
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