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dc.contributor.authorYokeş, Mehmet Baki
dc.contributor.authorAbatay Sel, Figen
dc.contributor.authorKıvanç, Demet
dc.contributor.authorÇınar, Çiğdem
dc.contributor.authorPehlivan, Sacide
dc.contributor.authorOğuz, Fatma
dc.contributor.authorŞentürk Çiftçi, Hayriye
dc.contributor.authorÖzdilli, Kürşat
dc.contributor.authorDuvarcı Öğret, Yeliz
dc.contributor.authorOğuz, Süleyman Rüştü
dc.contributor.authorİşsever, Halim
dc.date.accessioned2022-07-04T12:06:19Z
dc.date.available2022-07-04T12:06:19Z
dc.date.issued2022
dc.identifier.citationÖzdilli K., Duvarcı Öğret Y., Oğuz S. R. , İşsever H., Yokeş M. B. , Şentürk Çiftçi H., Abatay Sel F., Kıvanç D., Çınar Ç., Pehlivan S., et al., "GENETIC POLYMORPHISMS IN 15 STR LOCI IN THE TURKISH POPULATION LIVING IN ISTANBUL PROVINCE", Nobel medicus, cilt.18, sa.1, ss.54-61, 2022
dc.identifier.issn1305-2381
dc.identifier.otherav_0ce20b4a-56c2-4a4e-bb3a-05b67c5b38b5
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/181575
dc.identifier.urihttps://www.nobelmedicus.com/tr/Makale.aspx?m=1721
dc.description.abstractObjective: Short tandem repeats (STRs) are short sequences of nucleotides that are repeated and distributed all over the genome. These polymorphisms enable investigation of the forensic, ancestral lineage and evolutionary studies in human population. Owing to the historical migration and ethnic groups, it is very valuable to evaluate genetic distances in Turkey. The aim of the present study is to examine the STR data of Istanbul and compare the genetic distances and allele frequency with the previously published data of 27 countries from Europe, Asia, America, Africa and Middle East. Material and Method: Peripheral blood samples were obtained from 400 healthy individuals. DNA samples were amplified using a commercial kit. Multiplex STRPCR (Applied Biosystems, Foster City, CA, USA) was used and the amplicons were evaluated on an ABI 3130 Genetic Analyzer. Results: Among all loci, D21S11 and D18S51 were the most polymorphic loci. The power of discrimination (PD) ranged from 0.8329 (TPOX) to 0.9722 (D18S51). The combined PD and probability of exclusion (PE) were found to be >0.99999999 and 0.99999671, respectively. Conclusion: In this study, six STR markers were selected to compare the genetic distances and allele frequency of the present results with the results of twenty-seven studies which were published previously. This study indicates that the population in Turkey is an intermediate between Europe, Middle East and Central Asia. Keywords: Human genetics, polymorphism, population genetics, short tandem repeat.
dc.language.isoeng
dc.subjectMedicine (miscellaneous)
dc.subjectKlinik Tıp (MED)
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp
dc.subjectBiyoloji ve Biyokimya
dc.subjectTIP, GENEL & İÇECEK
dc.subjectBİYOLOJİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectTıbbi Biyoloji
dc.subjectFamily Practice
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectInternal Medicine
dc.subjectAssessment and Diagnosis
dc.subjectGeneral Medicine
dc.subjectHealth Sciences
dc.titleGENETIC POLYMORPHISMS IN 15 STR LOCI IN THE TURKISH POPULATION LIVING IN ISTANBUL PROVINCE
dc.typeMakale
dc.relation.journalNobel medicus
dc.contributor.departmentHaliç Üniversitesi , Hemşirelik Yüksekokulu ,
dc.identifier.volume18
dc.identifier.issue1
dc.identifier.startpage54
dc.identifier.endpage61
dc.contributor.firstauthorID3415976


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