ameloblastoma/carbohydrate

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

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Logi sisse

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

The importance of BRAF-V600E mutation to ameloblastoma metabolism.

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Logi sisse

Ameloblastoma is a locally infiltrative, aggressive epithelial odontogenic neoplasm. BRAF-V600E mutation is frequently found in this tumor and has a pivotal role in its pathogenesis, but the consequences of this alteration need to be addressed. An untargeted metabolomics approach was

Lectin histochemistry of ameloblastomas and odontogenic keratocysts.

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Logi sisse

The cell membrane carbohydrate components of 10 simple (follicular and/or plexiform pattern) and 5 acanthomatous ameloblastomas, one plexiform unicystic ameloblastoma, one soft tissue ameloblastoma and 11 odontogenic keratocysts were studied in paraffin-embedded tissues using horseradish

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

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Logi sisse

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

A study of lectin histochemistry in ameloblastoma.

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Logi sisse

The lectin histochemistry of ameloblastoma was investigated in order to understand the nature of the carbohydrate residues in this tumor, in accordance with the WHO subclassification. Mannose and glucose were generally common in almost all cells in both the follicular and plexiform types, especially

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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Logi sisse

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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