rdf:type |
|
lifeskim:mentions |
umls-concept:C0007137,
umls-concept:C0027627,
umls-concept:C0079419,
umls-concept:C0086661,
umls-concept:C0205225,
umls-concept:C0242957,
umls-concept:C0314603,
umls-concept:C0439064,
umls-concept:C0442027,
umls-concept:C0449438,
umls-concept:C1414313,
umls-concept:C1515926,
umls-concept:C1707513,
umls-concept:C2603343
|
pubmed:issue |
5
|
pubmed:dateCreated |
2010-10-27
|
pubmed:abstractText |
Oncogenesis in the oral cavity is believed to result from genetic alterations that cause a stepwise transformation of the mucosa to invasive carcinoma. In oral squamous cell carcinoma (OSCC) multiple cytogenetic abnormalities have been reported, but their practical significance remains uncertain.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCND1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin D1,
http://linkedlifedata.com/resource/pubmed/chemical/ERBB2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/MYC protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-myc,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, erbB-2,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
1365-2133
|
pubmed:author |
pubmed-author:Alameda QuitlletFF,
pubmed-author:BaróTT,
pubmed-author:EspinetBB,
pubmed-author:Garcia-MuretMM,
pubmed-author:GilaberteMM,
pubmed-author:Martín-EzquerraGG,
pubmed-author:PujolR MRM,
pubmed-author:SalgadoRR,
pubmed-author:SoléFF,
pubmed-author:TollAA,
pubmed-author:YébenesMM
|
pubmed:copyrightInfo |
© 2010 The Authors. BJD © 2010 British Association of Dermatologists.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
163
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1028-35
|
pubmed:meshHeading |
pubmed-meshheading:20662834-Adult,
pubmed-meshheading:20662834-Aged,
pubmed-meshheading:20662834-Aged, 80 and over,
pubmed-meshheading:20662834-Biopsy,
pubmed-meshheading:20662834-Carcinoma, Squamous Cell,
pubmed-meshheading:20662834-Cyclin D1,
pubmed-meshheading:20662834-Female,
pubmed-meshheading:20662834-Gene Dosage,
pubmed-meshheading:20662834-Genes, p53,
pubmed-meshheading:20662834-Humans,
pubmed-meshheading:20662834-Lymph Nodes,
pubmed-meshheading:20662834-Male,
pubmed-meshheading:20662834-Middle Aged,
pubmed-meshheading:20662834-Mouth Neoplasms,
pubmed-meshheading:20662834-Neoplasm Metastasis,
pubmed-meshheading:20662834-Oncogenes,
pubmed-meshheading:20662834-Proto-Oncogene Proteins c-myc,
pubmed-meshheading:20662834-Receptor, Epidermal Growth Factor,
pubmed-meshheading:20662834-Receptor, erbB-2,
pubmed-meshheading:20662834-Tumor Markers, Biological
|
pubmed:year |
2010
|
pubmed:articleTitle |
Multiple genetic copy number alterations in oral squamous cell carcinoma: study of MYC, TP53, CCDN1, EGFR and ERBB2 status in primary and metastatic tumours.
|
pubmed:affiliation |
Department of Medicina i Dermatologia, Universitat Autònoma de Barcelona, Hospital del Mar, Parc de Salut Mar, Passeig Marítim 25-29, 08003 Barcelona, Spain. gmartin@parcdesalutmar.cat
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|