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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/17992
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dc.contributor.authorPatsalis, P. C.en
dc.contributor.authorHadjimarcou, M. I.en
dc.contributor.authorVelissariou, V.en
dc.contributor.authorKitsiou-Tzeli, S.en
dc.contributor.authorZera, C.en
dc.contributor.authorSyrrou, M.en
dc.contributor.authorLyberatou, E.en
dc.contributor.authorTsezou, A.en
dc.contributor.authorGalla, A.en
dc.contributor.authorSkordis, N.en
dc.date.accessioned2015-11-24T18:49:39Z-
dc.date.available2015-11-24T18:49:39Z-
dc.identifier.issn0009-9163-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/17992-
dc.rightsDefault Licence-
dc.subjectCell Cycle Proteinsen
dc.subjectDNA Primersen
dc.subjectDNA-Binding Proteins/geneticsen
dc.subjectFemaleen
dc.subjectGenetic Markersen
dc.subjectHumansen
dc.subjectIn Situ Hybridization, Fluorescenceen
dc.subjectKaryotypingen
dc.subject*Nuclear Proteinsen
dc.subjectRNA-Binding Proteins/geneticsen
dc.subjectSequence Analysis, DNAen
dc.subjectSex-Determining Region Y Proteinen
dc.subject*Transcription Factorsen
dc.subjectTurner Syndrome/*geneticsen
dc.subjectY Chromosomeen
dc.titleSupernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosomeen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/9137884-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1111/j.1399-0004.1997.tb02450.x/asset/j.1399-0004.1997.tb02450.x.pdf?v=1&t=h0disu8y&s=d4787bbb736e757533536a8050116e16801f3fd9-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1997-
heal.abstractDNA and FISH (fluorescence in situ hybridization) analysis were carried out in 12 patients with stigmata of Turner syndrome to determine whether the Supernumerary Marker Chromosome (SMC) found cytogenetically in each of these patients was derived from the Y chromosome. The presence of a Y chromosome in these patients may predispose them to develop gonadoblastoma. PCR-Southern blot analysis, followed by FISH, was used to detect the presence of Y chromosome material. The Sex determining Region Y (SRY), Testis Specific Protein Y-encoded (TSPY) and Y-chromosome RNA Recognition Motif (YRRM) genes, which map at Yp11.31, Yp11.1-11.2 and Yp11.2/Yq11.21-11.23, respectively, were selected as markers, because they span the whole Y chromosome, and more importantly, they are considered to be involved in the development of gonadoblastoma. It was shown that in 12 patients, all of whom had an SMC, the SMC of 11 was derived from the Y chromosome. Furthermore, the presence of the SRY, TSPY and YRRM gene sequences was determined and FISH analysis confirmed the Y origin of the SMCs. The methodology described in this report is a rapid, reliable and sensitive approach which may be easily applied to determine the Y origin of an SMC carried in Turner syndrome. The identification of an SMC is important for the clinical management and prognostic counseling of these patients with Turner syndrome.en
heal.journalNameClin Geneten
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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