Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/14639
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dc.contributor.authorFiratligil, Fahri Burcin-
dc.contributor.authorYildirir, Burcu Firatligil-
dc.contributor.authorYalcin-Ozuysal, Ozden-
dc.date.accessioned2024-09-24T15:44:16Z-
dc.date.available2024-09-24T15:44:16Z-
dc.date.issued2024-
dc.identifier.issn0104-4230-
dc.identifier.issn1806-9282-
dc.identifier.urihttps://doi.org/10.1590/1806-9282.20231673-
dc.descriptionYalcin-Ozuysal, Ozden/0000-0003-0552-368X; FIRATLIGIL, Fahri Burcin/0000-0002-4499-3492en_US
dc.description.abstractOBJECTIVE: Investigating the potential role of CYR61 in recurrent pregnancy loss is critical for developing diagnostic approaches and treatments for recurrent pregnancy loss. METHODS: In this prospective case-control study, we have investigated the expression patterns of CYR61 in blood samples from participants with recurrent pregnancy loss in their medical history and control group (n=20 vs n=10). Peripheral blood mononuclear cells from study and control groups were isolated and the expression patterns of the CYR61 gene were determined by real-time semi-quantitative reverse transcriptase PCR. RESULTS: A significant decrease in CYR61 gene expression was demonstrated in patients with two or more clinically recognized miscarriages compared with patients without miscarriages or with a history of miscarriage (p<0.01), which may make the CYR61 gene a potential candidate for predicting the risk of recurrent pregnancy loss. DISCUSSION: This study provides a basis for a detailed investigation of candidate biomarkers and molecular players involved in the development of recurrent pregnancy loss and for the development of potential treatment approaches to prevent recurrent pregnancy loss.en_US
dc.description.sponsorshipWe are grateful to all participants and their families who spent their precious time and participated in this research program. We are also thankful for the tireless efforts of the research team members.en_US
dc.language.isoenen_US
dc.publisherAssoc Medica Brasileiraen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCytogeneticsen_US
dc.subjectMiscarriageen_US
dc.subjectMolecular geneticsen_US
dc.titleA new insight into the pathway behind spontaneous recurrent pregnancy loss: decreased CYR61 gene expressionen_US
dc.typeArticleen_US
dc.authoridYalcin-Ozuysal, Ozden/0000-0003-0552-368X-
dc.authoridFIRATLIGIL, Fahri Burcin/0000-0002-4499-3492-
dc.departmentIzmir Institute of Technologyen_US
dc.identifier.volume70en_US
dc.identifier.issue6en_US
dc.identifier.wosWOS:001275940900001-
dc.identifier.scopus2-s2.0-85199385337-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1590/1806-9282.20231673-
dc.identifier.pmid39045957-
dc.authorscopusid55892313700-
dc.authorscopusid59117012000-
dc.authorscopusid35777178800-
dc.authorwosidYalcin Ozuysal, Ozden/D-5528-2019-
dc.authorwosidFIRATLIGIL, Fahri Burcin/O-9920-2014-
dc.identifier.wosqualityQ4-
dc.identifier.scopusqualityQ2-
dc.description.woscitationindexScience Citation Index Expanded-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
crisitem.author.dept04.03. Department of Molecular Biology and Genetics-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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