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dc.contributor.authorGohari-Lasaki, S
dc.contributor.authorGharesouran, J
dc.contributor.authorGhojazadeh, M
dc.contributor.authorMontazeri, V
dc.contributor.authorMohaddes Ardebili, SM
dc.date.accessioned2018-08-26T05:45:29Z
dc.date.available2018-08-26T05:45:29Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/40940
dc.description.abstractTP53 is assumed to be a very important tumour suppressor gene, as illustrated by recent reports that have shown effects of its polymorphisms on breast cancer risk. Arg72Pro and PIN3(16bp duplication) polymorphisms are proposed to have an effective role in structural changes of p53 and have therefore attracted interest as a risk factor for breast cancer in different populations. The aim of this study was to examine and determine whether p53 codon 72 and PIN3 Ins16 bp may be associated with an increased risk for breast cancer in female patients from the northwest of Iran. Genotyping was performed by PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism) method for a total of 100 women with breast cancer and 100 healthy women without any background of cancer, focusing on the TP53 Arg72Pro-16Del/Ins haplotypes and the combined genotypes. The results in this study established no statistical significant distinctions between the genotypes and allele frequency were found for Arg72Pro and PIN3 Ins 16 bp polymorphisms between patients and controls.
dc.language.isoEnglish
dc.relation.ispartofAsian Pacific journal of cancer prevention : APJCP
dc.subjectAdult
dc.subjectBreast Neoplasms
dc.subjectCase-Control Studies
dc.subjectCodon
dc.subjectFemale
dc.subjectGene Duplication
dc.subjectGene Frequency
dc.subjectGenetic Predisposition to Disease
dc.subjectGenotype
dc.subjectHumans
dc.subjectIran
dc.subjectPolymorphism, Genetic
dc.subjectRisk
dc.subjectRisk Factors
dc.subjectTumor Suppressor Protein p53
dc.titleLack of influence of TP53 Arg72Pro and 16bp duplication polymorphisms on risk of breast cancer in Iran.
dc.typearticle
dc.citation.volume16
dc.citation.issue7
dc.citation.spage2971
dc.citation.epage4
dc.citation.indexPubmed


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