rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
5
|
pubmed:dateCreated |
2009-1-8
|
pubmed:abstractText |
DNA polymerases (Pols) represent potential candidates for cancer genes because of their central functions in DNA metabolism. Defects of some DNA Pols have shown cancer associations, but data on DNA polymerase (Pol) epsilon is limited.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1109-6535
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
5
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
287-92
|
pubmed:meshHeading |
pubmed-meshheading:19129559-Breast Neoplasms,
pubmed-meshheading:19129559-DNA, Neoplasm,
pubmed-meshheading:19129559-DNA Polymerase II,
pubmed-meshheading:19129559-DNA Primers,
pubmed-meshheading:19129559-Exons,
pubmed-meshheading:19129559-Female,
pubmed-meshheading:19129559-Genome, Human,
pubmed-meshheading:19129559-Humans,
pubmed-meshheading:19129559-Introns,
pubmed-meshheading:19129559-Polymerase Chain Reaction,
pubmed-meshheading:19129559-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:19129559-Sequence Deletion
|
pubmed:articleTitle |
Genomic changes of the 55 kDa subunit of DNA polymerase epsilon in human breast cancer.
|
pubmed:affiliation |
Department of Pathology, University of Turku, Finland.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|