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dc.contributor.authorTorkamandi, S
dc.contributor.authorBastami, M
dc.contributor.authorGhaedi, H
dc.contributor.authorMoghadam, F
dc.contributor.authorMirfakhraie, R
dc.contributor.authorOmrani, MD
dc.date.accessioned2018-08-26T05:05:44Z
dc.date.available2018-08-26T05:05:44Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39383
dc.description.abstractConsidering that MAPK (mitogen- activated protein kinase) signaling pathway has an important role in the progression of inflammatory cytokine secretion in type 2 diabetes mellitus (T2DM), we have recently investigated the reported genetic polymorphism from genome wide association study in MAP3K1 (mitogen-activated protein kinase kinase kinase 1) in diabetes as an important member of MAPK signaling. This study aimed to investigate the possible association of rs10461617 at the upstream of MAP3K1 gene in an Iranian case-control study with the risk of T2DM. The study population was comprised of 342 unrelated Iranian individuals including 177 patients with T2DM and 165 unrelated healthy control subjects. Genotyping was performed using PCR-RFLP and confirmed with sequencing. In a logistic regression analysis, the rs10461617A allele was associated with a significantly higher risk of T2DM assuming the log- additive model (OR: 1.44, 95% CI: 1.01-2.05, P = 0.039). In conclusion, we provided the first evidence for the association of rs10461617 at the upstream of MAP3K1 with the risk of T2DM in an Iranian population.
dc.language.isoEnglish
dc.relation.ispartofInternational journal of molecular and cellular medicine
dc.titleMAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population.
dc.typearticle
dc.citation.volume5
dc.citation.issue3
dc.citation.spage134
dc.citation.epage140
dc.citation.indexPubmed


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