Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2009-3-9
pubmed:abstractText
To investigate whether the gene polymorphisms for p21, X-ray repair cross-complementing group 1 (XRCC1), human 8-oxoguanine glycosylase 1 (hOGG1), and dopamine D1 and D2 receptors (DRD1, -2) are associated with leiomyoma susceptibility.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1556-5653
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
91
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
869-77
pubmed:meshHeading
pubmed-meshheading:19176223-Case-Control Studies, pubmed-meshheading:19176223-Codon, pubmed-meshheading:19176223-Cyclin-Dependent Kinase Inhibitor p21, pubmed-meshheading:19176223-DNA Glycosylases, pubmed-meshheading:19176223-DNA-Binding Proteins, pubmed-meshheading:19176223-Female, pubmed-meshheading:19176223-Gene Expression Regulation, Enzymologic, pubmed-meshheading:19176223-Gene Expression Regulation, Neoplastic, pubmed-meshheading:19176223-Gene Frequency, pubmed-meshheading:19176223-Genetic Predisposition to Disease, pubmed-meshheading:19176223-Humans, pubmed-meshheading:19176223-Leiomyoma, pubmed-meshheading:19176223-Polymorphism, Genetic, pubmed-meshheading:19176223-Prospective Studies, pubmed-meshheading:19176223-Receptors, Dopamine D1, pubmed-meshheading:19176223-Receptors, Dopamine D2, pubmed-meshheading:19176223-Uterine Neoplasms
pubmed:year
2009
pubmed:articleTitle
The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma.
pubmed:affiliation
Department of Obstetrics and Gynecology, China Medical University Hospital, Taipei, Taiwan, People's Republic of China.
pubmed:publicationType
Journal Article