Publication: Male infertility in Sertoli cell-only syndrome: An investigation of autosomal gene defects
dc.contributor.author | GÜNEY, AHMET İLTER | |
dc.contributor.authors | Koc, Gulsah; Ozdemir, Abdullah A.; Girgin, Gozde; Akbal, Cem; Kirac, Deniz; Avcilar, Tuba; Guney, Ahmet I. | |
dc.date.accessioned | 2022-03-14T09:18:09Z | |
dc.date.available | 2022-03-14T09:18:09Z | |
dc.date.issued | 2019-02 | |
dc.description.abstract | Objectives To detect autosomal genetic defects and to determine candidate genes in Sertoli cell-only syndrome infertile men. Methods Single-nucleotide polymorphism + comparative genomic hybridization microarray technology was carried out on 39 Sertoli cell-only syndrome infertile patients in the present study. Array comparative genomic hybridization compares the patient's genome against a reference genome, and identifies uncover deletions, amplifications and loss of heterozygosity. Results A link between defective spermatogenesis genes and infertility was examined, and amplifications and deletions in several genes were detected, including homeobox gene; synaptonemal complex element protein 1; collagen, type I, alpha 1; imprinted maternally expressed transcript; and potassium voltage-gated channel subfamily Q member 1. Conclusions The present data suggest that several genes can play an important role in spermatogenesis and progression of Sertoli cell-only syndrome. | |
dc.identifier.doi | 10.1111/iju.13863 | |
dc.identifier.eissn | 1442-2042 | |
dc.identifier.issn | 0919-8172 | |
dc.identifier.pubmed | 30478911 | |
dc.identifier.uri | https://hdl.handle.net/11424/242937 | |
dc.identifier.wos | WOS:000457782400024 | |
dc.language.iso | eng | |
dc.publisher | WILEY | |
dc.relation.ispartof | INTERNATIONAL JOURNAL OF UROLOGY | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | array comparative genomic hybridization | |
dc.subject | infertility | |
dc.subject | Sertoli cell-only syndrome | |
dc.subject | DNA METHYLATION | |
dc.subject | EXPRESSION | |
dc.subject | PATTERNS | |
dc.subject | MEIOSIS | |
dc.title | Male infertility in Sertoli cell-only syndrome: An investigation of autosomal gene defects | |
dc.type | article | |
dspace.entity.type | Publication | |
local.avesis.id | 4d298467-064a-46e1-b9bd-6667ecf80e19 | |
local.import.package | SS16 | |
local.indexed.at | WOS | |
local.indexed.at | SCOPUS | |
local.indexed.at | PUBMED | |
local.journal.numberofpages | 7 | |
local.journal.quartile | Q2 | |
oaire.citation.endPage | 298 | |
oaire.citation.issue | 2 | |
oaire.citation.startPage | 292 | |
oaire.citation.title | INTERNATIONAL JOURNAL OF UROLOGY | |
oaire.citation.volume | 26 | |
relation.isAuthorOfPublication | d474fc8a-ae88-487e-b63b-7f506191fb94 | |
relation.isAuthorOfPublication.latestForDiscovery | d474fc8a-ae88-487e-b63b-7f506191fb94 |
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