radicular cyst/carbohydrate

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Inability to distinguish ameloblastomas from odontogenic cysts based on expression of blood cell carbohydrates.

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This study was designed to confirm the report by Vedtofte and coworkers that the epithelium of ameloblastomas can be distinguished from that of nonneoplastic odontogenic cysts by differences in expressivity of cell surface carbohydrates with blood group specificity. Immunoperoxidase techniques were

Relation of blood group carbohydrates to differentiation patterns of normal and pathological odontogenic epithelium.

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The distribution of epithelial cell surface antigens was studied in normal odontogenic epithelium from 20 fetuses and in odontogenic epithelium from 15 ameloblastomas, 16 odontogenic keratocysts, 15 follicular and 15 radicular cysts. The cell surface carbohydrates were detected using antibodies with

Enzyme-labeled Antigen Method: Development and Application of the Novel Approach for Identifying Plasma Cells Locally Producing Disease-specific Antibodies in Inflammatory Lesions.

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In chronic inflammatory lesions of autoimmune and infectious diseases, plasma cells are frequently observed. Antigens recognized by antibodies produced by the plasma cells mostly remain unclear. A new technique identifying these corresponding antigens may give us a breakthrough for understanding the

Distribution of type 1 and 2 blood group chains in normal and pathological odontogenic epithelium defined by monoclonal antibodies specific for Lea and H type 2.

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This study describes the distribution of type 1 and type 2 blood group carbohydrate chains in human normal and pathological odontogenic epithelia and in epithelia of human oral mucosa. Odontogenic epithelium was examined from 12 fetal tooth germs, 25 ameloblastomas, 13 odontogenic keratocysts, 13

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