Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25681
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dc.date.accessioned2022-04-11T06:08:34Z-
dc.date.available2022-04-11T06:08:34Z-
dc.date.issued2012-11-01-
dc.identifier.citationCander, S. vd. (2012). "Effect of cycline D1 (CCND1) gene polymorphism on tumor formation and behavior in patients with prolactinoma". Gene, 509(1), 158-163.en_US
dc.identifier.issn0378-1119-
dc.identifier.issn1879-0038-
dc.identifier.urihttps://doi.org/10.1016/j.gene.2012.07.056-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0378111912009079-
dc.identifier.urihttp://hdl.handle.net/11452/25681-
dc.description.abstractThe objective of this study was to investigate the effect of G870A gene polymorphism of CCND1 on the formation and behavioral features of prolactinomas. One hundred and thirteen patients with prolactinoma and 108 age and gender matched control were included in the study. The patients were divided into two groups as noninvasive and invasive tumors. CCND1 G870A gene polymorphism was compared in patients/control and invasive/noninvasive groups. A and G allele frequencies were found as 41.7% and 58.3% in the controls, and 61.1% and 38.9% in the patients (p<0.01). Rates of G/G, G/A and A/A genotypes were found as 11.8%, 55.9% and 32.4% in the noninvasive group, and 15.6%, 44.4% and 40.0% in the invasive group, respectively. Differences between patient and control groups were significant but were not between invasive and noninvasive groups in terms of the allele frequencies and genotype distribution. Mean tumor size and serum levels of prolactin at the time of diagnosis and change in these values after the treatment were not found statistically significant in genotype subgroups. CCND1 G870A gene polymorphism may be an important factor in the early stages of the tumor formation. However, it did not affect the features of the tumor.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGenetics & heredityen_US
dc.subjectProlactinomaen_US
dc.subjectPolymorphismen_US
dc.subjectInvasivenessen_US
dc.subjectCCND1en_US
dc.subjectSporadic pituitary-adenomasen_US
dc.subjectBreast-canceren_US
dc.subjectLung-canceren_US
dc.subjectExpressionen_US
dc.subjectOverexpressionen_US
dc.subjectClassificationen_US
dc.subjectCarcinomaen_US
dc.subjectGenotypeen_US
dc.subjectBiologyen_US
dc.subject.meshAdolescenten_US
dc.subject.meshAdulten_US
dc.subject.meshAgeden_US
dc.subject.meshBase sequenceen_US
dc.subject.meshCase-control studiesen_US
dc.subject.meshCross-sectional studiesen_US
dc.subject.meshCyclin d1en_US
dc.subject.meshDna primersen_US
dc.subject.meshFemaleen_US
dc.subject.meshGene frequencyen_US
dc.subject.meshHumansen_US
dc.subject.meshMagnetic resonance imagingen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshNeoplasm invasivenessen_US
dc.subject.meshPituitary neoplasmsen_US
dc.subject.meshPolymorphism, single nucleotideen_US
dc.subject.meshProlactinomaen_US
dc.subject.meshProto-oncogenesen_US
dc.subject.meshRetrospective studiesen_US
dc.subject.meshYoung adulten_US
dc.titleEffect of cycline D1 (CCND1) gene polymorphism on tumor formation and behavior in patients with prolactinomaen_US
dc.typeArticleen_US
dc.identifier.wos000309435400021tr_TR
dc.identifier.scopus2-s2.0-84866171305tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Endokrinoloji ve Metabolizma Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.tr_TR
dc.identifier.startpage158tr_TR
dc.identifier.endpage163tr_TR
dc.identifier.volume509tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalGeneen_US
dc.contributor.buuauthorCander, Soner-
dc.contributor.buuauthorErtürk, Erdinç-
dc.contributor.buuauthorKarkucak, Mutlu-
dc.contributor.buuauthorGül, Özen Öz-
dc.contributor.buuauthorGörükmez, Orhan-
dc.contributor.buuauthorYakut, Tahsin-
dc.contributor.buuauthorÜnal, Oğuz Kaan-
dc.contributor.buuauthorErsoy, Canan-
dc.contributor.buuauthorTuncel, Ercan-
dc.contributor.buuauthorİmamoğlu, Şazi-
dc.contributor.researcheridAAI-1005-2021tr_TR
dc.contributor.researcheridAAH-8861-2021tr_TR
dc.contributor.researcheridAAJ-6536-2021tr_TR
dc.identifier.pubmed22967707tr_TR
dc.subject.wosGenetics & heredityen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid25027068600tr_TR
dc.contributor.scopusid7005488796tr_TR
dc.contributor.scopusid35388323500tr_TR
dc.contributor.scopusid26040787100tr_TR
dc.contributor.scopusid56681045900tr_TR
dc.contributor.scopusid6602802424tr_TR
dc.contributor.scopusid55042241400tr_TR
dc.contributor.scopusid6701485882tr_TR
dc.contributor.scopusid7006929833tr_TR
dc.contributor.scopusid6602297533tr_TR
dc.subject.scopusRibociclib; Cyclin Dependent Kinase 4; Hormone Receptorsen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCarcinogenesisen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCyclin d1 geneen_US
dc.subject.emtreeDna polymorphismen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGeneen_US
dc.subject.emtreeGene frequencyen_US
dc.subject.emtreeGenotypeen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman tissueen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNuclear magnetic resonance imagingen_US
dc.subject.emtreePatient attitudeen_US
dc.subject.emtreePolymerase chain reactionen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeProlactinomaen_US
dc.subject.emtreeTumor volumeen_US
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