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DC Field | Value | Language |
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dc.contributor.author | P. A. Reichart | en_US |
dc.contributor.author | H. P. Philipsen | en_US |
dc.contributor.author | P. Khongkhunthian | en_US |
dc.contributor.author | J. J. Sciubba | en_US |
dc.date.accessioned | 2018-09-05T03:36:11Z | - |
dc.date.available | 2018-09-05T03:36:11Z | - |
dc.date.issued | 2017-09-01 | en_US |
dc.identifier.issn | 16010825 | en_US |
dc.identifier.issn | 1354523X | en_US |
dc.identifier.other | 2-s2.0-84994344562 | en_US |
dc.identifier.other | 10.1111/odi.12572 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994344562&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/57180 | - |
dc.description.abstract | © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd This study was focused on the immunohistochemical profile of the adenomatoid odontogenic tumor. A Pub/Medline search revealed a number of immunohistochemical studies including cytokeratin profiles, extracellular matrix proteins, Integrins, ameloblast-associated proteins resorption regulators (RANK, RANKL), p53, PCNA, MDM2 protein, cyclin D1, Ki-67, Bcl-2 metallothionein, metalloproteinases, D56 hepatocyte growth factor, c-met, DNA methyltransferase, podoplanin, TGF-βI, Smad-2/3, Smad-I-5/-8, Smad 4, beta- catenin, calretinin, and clonality. Careful interpretation of the findings indicates that the adenomatoid odontogenic tumor may be more of a hamartomatous than neoplastic nature. | en_US |
dc.subject | Dentistry | en_US |
dc.subject | Medicine | en_US |
dc.title | Immunoprofile of the adenomatoid odontogenic tumor | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Oral Diseases | en_US |
article.volume | 23 | en_US |
article.stream.affiliations | Charité – Universitätsmedizin Berlin | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Greater Baltimore Medical Center | en_US |
Appears in Collections: | CMUL: Journal Articles |
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