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dc.contributor.authorP. A. Reicharten_US
dc.contributor.authorH. P. Philipsenen_US
dc.contributor.authorP. Khongkhunthianen_US
dc.contributor.authorJ. J. Sciubbaen_US
dc.date.accessioned2018-09-05T03:36:11Z-
dc.date.available2018-09-05T03:36:11Z-
dc.date.issued2017-09-01en_US
dc.identifier.issn16010825en_US
dc.identifier.issn1354523Xen_US
dc.identifier.other2-s2.0-84994344562en_US
dc.identifier.other10.1111/odi.12572en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994344562&origin=inwarden_US
dc.identifier.urihttp://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.subjectDentistryen_US
dc.subjectMedicineen_US
dc.titleImmunoprofile of the adenomatoid odontogenic tumoren_US
dc.typeJournalen_US
article.title.sourcetitleOral Diseasesen_US
article.volume23en_US
article.stream.affiliationsCharité – Universitätsmedizin Berlinen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsGreater Baltimore Medical Centeren_US
Appears in Collections:CMUL: Journal Articles

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