rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
2008-4-14
|
pubmed:abstractText |
Dupuytren's disease (DD) is a hand disease inherited as an autosomal dominant trait with variable penetrance, especially among populations of northern European ancestry. The etiology and pathophysiology of DD are not clear. The purpose of this study was to examine the gene expression profiles of palmar fascia of DD and healthy patients using microarray analysis to highlight the genes that might contribute to the pathogenesis of DD.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0022-4804
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
146
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
271-5
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:17996904-Adult,
pubmed-meshheading:17996904-Aged,
pubmed-meshheading:17996904-Blotting, Far-Western,
pubmed-meshheading:17996904-Dupuytren Contracture,
pubmed-meshheading:17996904-Female,
pubmed-meshheading:17996904-Gene Expression,
pubmed-meshheading:17996904-Genetic Predisposition to Disease,
pubmed-meshheading:17996904-Humans,
pubmed-meshheading:17996904-Immunohistochemistry,
pubmed-meshheading:17996904-Male,
pubmed-meshheading:17996904-Middle Aged,
pubmed-meshheading:17996904-Myoglobin,
pubmed-meshheading:17996904-Receptor Tyrosine Kinase-like Orphan Receptors,
pubmed-meshheading:17996904-Receptors, Cell Surface
|
pubmed:year |
2008
|
pubmed:articleTitle |
The expression of myoglobin and ROR2 protein in Dupuytren's disease.
|
pubmed:affiliation |
Department of Surgery, Oulu University, Oulu, Finland. minna.forsman@ppshp.fi
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|