Bu öğeden alıntı yapmak, öğeye bağlanmak için bu tanımlayıcıyı kullanınız:
http://hdl.handle.net/11452/22404
Tüm üstveri kaydı
Dublin Core Alanı | Değer | Dil |
---|---|---|
dc.contributor.author | Erçelen, Nesrin | - |
dc.contributor.author | Acar, Hasan | - |
dc.date.accessioned | 2021-10-19T08:10:49Z | - |
dc.date.available | 2021-10-19T08:10:49Z | - |
dc.date.issued | 2006-05-15 | - |
dc.identifier.citation | Yakut, T. vd. (2006). ''Meiotic segregation analysis of reciprocal translocations, both in sperms and blastomeres''. American Journal of Medical Genetics, 140A(10), 1074-1082. | en_US |
dc.identifier.issn | 1552-4825 | - |
dc.identifier.uri | https://doi.org/10.1002/ajmg.a.31215 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.31215 | - |
dc.identifier.uri | http://hdl.handle.net/11452/22404 | - |
dc.description.abstract | Balanced chromosomal rearrangements could lead to unbalanced segregation gametes during meiosis. In this Study, sperm flourescence ill situ hybridization (FISH) analysis of meiotic segregation products of four reciprocal translocations; 46,XY,t(7;10)(q21;q22), 46:XY,t(15;17)(q11;p12), 46,XY, t(6;13)(p21.1;q32), and 46,XY,t(1;13)(q24;q10) are presented. In three Out Of these four cases with t(15;17), t(6;13), and t(1;13) additional blastomere FISH analyses are also provided. multi-color FISH analysis was applied using diverse probe combinations specific for translocated chromosome segments. The average frequency of sperm nuclei bearing unbalanced products for t(7;10), t(15:17), t(6;13), and t(1;13) were 48.7%, 59.5%, 60.5%, and 62.9%, respectively. Frequencies of blastomeres comprising unbalanced products in Cases with t(15;17), t(6;13), and t(1:13) were 80% (12 of 15), 60% (3 of 5), and 50% (2 of 4), respectively. Chi-square test analysis showed significant differences in the meiotic segregation pattens Clue to the distribution and numbers of the chiasmatas that Could depend oil the size of the translocated segments (P < 0.001). In conclusion, FISH analysis of sperm and blastomere for reciprocal translocation carriers effectively estimates the approximate risk Of unbalanced products and this result might ensure Valuable genetic Counseling. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Genetics & heredity | en_US |
dc.subject | Sperm | en_US |
dc.subject | Reciprocal translocation | en_US |
dc.subject | Meiotic segregation | en_US |
dc.subject | Blastomere | en_US |
dc.subject | Patterns | en_US |
dc.subject | Diagnosis | en_US |
dc.subject | Aneuploidy | en_US |
dc.subject | Spermatozoa | en_US |
dc.subject | Fish | en_US |
dc.subject | Heterozygotes | en_US |
dc.subject | Carriers | en_US |
dc.subject | Cytogenetic analysis | en_US |
dc.subject | Chromosome segregation | en_US |
dc.subject | In-situ hybridization | en_US |
dc.subject.mesh | Translocation, genetic | en_US |
dc.subject.mesh | Spermatozoa | en_US |
dc.subject.mesh | Models, genetic | en_US |
dc.subject.mesh | Meiosis | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Karyotyping | en_US |
dc.subject.mesh | Infertility, male | en_US |
dc.subject.mesh | In situ hybridization, fluorescence | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Chromosome segregation | en_US |
dc.subject.mesh | Blastomeres | en_US |
dc.title | Meiotic segregation analysis of reciprocal translocations, both in sperms and blastomeres | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000237171100006 | tr_TR |
dc.identifier.scopus | 2-s2.0-33646230293 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Jinekoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0001-7904-883X | tr_TR |
dc.identifier.startpage | 1074 | tr_TR |
dc.identifier.endpage | 1082 | tr_TR |
dc.identifier.volume | 140A | tr_TR |
dc.identifier.issue | 10 | tr_TR |
dc.relation.journal | American Journal of Medical Genetics | en_US |
dc.contributor.buuauthor | Yakut, Tahsin | - |
dc.contributor.buuauthor | Kimya, Yalçın | - |
dc.contributor.buuauthor | Egeli, Ünal | - |
dc.contributor.researcherid | AAH-1420-2021 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.identifier.pubmed | 16596678 | tr_TR |
dc.subject.wos | Genetics & heredity | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q3 | en_US |
dc.contributor.scopusid | 6602802424 | tr_TR |
dc.contributor.scopusid | 6603919968 | tr_TR |
dc.contributor.scopusid | 55665145000 | tr_TR |
dc.subject.scopus | Robertsonian Chromosome Translocation; Preimplantation Genetic Diagnosis; Chromosome Aberrations | en_US |
dc.subject.emtree | Sperm | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Meiosis | en_US |
dc.subject.emtree | Karyotype 46, XY | en_US |
dc.subject.emtree | Human cell | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Heterozygote | en_US |
dc.subject.emtree | Genetic counseling | en_US |
dc.subject.emtree | Gene probe | en_US |
dc.subject.emtree | Gamete | en_US |
dc.subject.emtree | Fluorescence in situ hybridization | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Chromosome translocation | en_US |
dc.subject.emtree | Chromosome segregation | en_US |
dc.subject.emtree | Chromosome rearrangement | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Blastomere | en_US |
dc.subject.emtree | Cell nucleus | en_US |
dc.subject.emtree | Chromosome chiasm | en_US |
Koleksiyonlarda Görünür: | Scopus Web of Science |
Bu öğenin dosyaları:
Bu öğeyle ilişkili dosya bulunmamaktadır.
DSpace'deki bütün öğeler, aksi belirtilmedikçe, tüm hakları saklı tutulmak şartıyla telif hakkı ile korunmaktadır.