{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,4,1]],"date-time":"2024-04-01T19:41:54Z","timestamp":1712000514030},"reference-count":39,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2024,4,1]],"date-time":"2024-04-01T00:00:00Z","timestamp":1711929600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.fr","clinicalkey.jp","clinicalkey.es","clinicalkey.com.au","elsevier.es","clinicalkey.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Actas Urol\u00f3gicas Espa\u00f1olas (English Edition)"],"published-print":{"date-parts":[[2024,4]]},"DOI":"10.1016\/j.acuroe.2023.10.001","type":"journal-article","created":{"date-parts":[[2023,10,10]],"date-time":"2023-10-10T18:14:09Z","timestamp":1696961649000},"page":"246-253","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Correlation between LHCGR and NR5A1 genes polymorphism and male infertility risk"],"prefix":"10.1016","volume":"48","author":[{"given":"M.","family":"Behvarz","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.A.","family":"Rahmani","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Siasi Torbati","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Danaei Mehrabad","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Bikhof Torbati","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.acuroe.2023.10.001_bib0005","first-page":"497","article-title":"Genetics of male infertility: the new players","volume":"28","author":"Coutton","year":"2012","journal-title":"Med Sci."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0010","doi-asserted-by":"crossref","first-page":"342","DOI":"10.1080\/09513590.2018.1528220","article-title":"Association of IL-10, IL-18, and IL-33 genetic polymorphisms with recurrent pregnancy loss risk in Iranian women","volume":"35","author":"Soheilyfar","year":"2019","journal-title":"Gynecol Endocrinol."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0015","article-title":"Association of rubella, cytomegalovirus, and toxoplasma infections with recurrent miscarriages in Bonab-Iran: a case-control study","volume":"4","author":"Nasirpour","year":"2017","journal-title":"Gene Cell Tissue."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0020","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1016\/j.acuro.2019.10.013","article-title":"Diagnosis and hormonal treatment of male infertility","volume":"44","author":"Serrano","year":"2020","journal-title":"Actas Urol Esp."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0025","doi-asserted-by":"crossref","first-page":"1592","DOI":"10.1002\/humu.23312","article-title":"Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia","volume":"38","author":"Oud","year":"2017","journal-title":"Hum Mutat."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0030","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1186\/s12920-022-01197-w","article-title":"Association of CATSPER1, SPATA16, and TEX11 genes polymorphism with idiopathic azoospermia and oligospermia risk in Iranian population","volume":"15","author":"Behvarz","year":"2022","journal-title":"BMC Med Genom."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0035","article-title":"The effect of factor-xi (rs3756008) polymorphism on recurrent pregnancy loss in Iranian Azeri women","volume":"4","author":"Isazadeh","year":"2017","journal-title":"Gene Cell Tissue."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0040","article-title":"The effects of high and lowdoses of folic acid on oxidation of protein levels during pregnancy: a randomized double-blind clinical trial","volume":"33","author":"Shiralizadeh","year":"2017","journal-title":"Horm Mol Biol Clin Investig."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0045","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1515\/labmed-2017-0012","article-title":"Effects of coagulation factor XIII (Val34Leu) polymorphism on recurrent pregnancy loss in Iranian Azeri women","volume":"41","author":"Isazadeh","year":"2017","journal-title":"Laboratoriums Medizin."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0050","doi-asserted-by":"crossref","first-page":"881","DOI":"10.1016\/j.sjbs.2017.12.005","article-title":"Autosomal single-gene disorders involved in human infertility","volume":"25","author":"Jedidi","year":"2018","journal-title":"Saudi J Biol Sci."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0055","first-page":"314","article-title":"Surgical treatment for male infertility","volume":"44","author":"Serrano","year":"2020","journal-title":"Actas Urol Esp."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0060","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1007\/s00439-019-01974-1","article-title":"New insights into the genetics of spermatogenic failure: a review of the literature","volume":"138","author":"Cannarella","year":"2019","journal-title":"Hum Genet."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0065","first-page":"609","article-title":"Evaluation of inflammasome activation in peripheral blood mononuclear cells of hemodialysis treated patients with glomerulonephritis","volume":"20","author":"Hashemi","year":"2021","journal-title":"Iran J Pharm Res."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0070","doi-asserted-by":"crossref","first-page":"592","DOI":"10.1016\/j.fertnstert.2011.12.027","article-title":"High expression of luteinizing hormone receptors messenger RNA by human cumulus granulosa cells is in correlation with decreased fertilization","volume":"97","author":"Maman","year":"2012","journal-title":"Fertil Steril."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0075","doi-asserted-by":"crossref","first-page":"844","DOI":"10.1093\/molehr\/gau041","article-title":"Localization of luteinizing hormone receptor protein in the human ovary","volume":"20","author":"Yung","year":"2014","journal-title":"Mol Hum Reprod."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0080","doi-asserted-by":"crossref","first-page":"551","DOI":"10.1210\/edrv.21.5.0409","article-title":"Mutations of gonadotropins and gonadotropin receptors: elucidating the physiology and pathophysiology of pituitarygonadal function","volume":"21","author":"Themmen","year":"2000","journal-title":"Endocr Rev."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0085","first-page":"218","article-title":"Evaluation of the prevalence of exons 1 and 10 polymorphisms of LHCGR gene and its relationship with IVF success","volume":"20","author":"Javadi-Arjmand","year":"2019","journal-title":"J Reprod Infertil."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0090","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1007\/s12032-021-01561-3","article-title":"Isolation and characterization of a novel GRP78-specific single-chain variable fragment (scFv) using ribosome display method","volume":"38","author":"Shabani","year":"2021","journal-title":"Med Oncol."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0095","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1210\/edrv.18.3.0301","article-title":"Steroidogenic factor 1: a key determinant of endocrine development and function","volume":"18","author":"Parker","year":"1997","journal-title":"Endocr Rev."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0100","first-page":"654","article-title":"Developmental expression of mouse steroidogenic factor-1, an essential regulator of the steroid hydroxylases","volume":"8","author":"Ikeda","year":"1994","journal-title":"Mol Endocrinol."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0105","first-page":"643","article-title":"Functional difference between Ad4BP and ELP, and their distributions in steroidogenic tissues","volume":"8","author":"Morohashi","year":"1994","journal-title":"Mol Endocrinol."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0110","first-page":"1671","article-title":"Shedding light on triple-negative breast cancer with Trop2-targeted antibody-drug conjugates","volume":"12","author":"Kaboli","year":"2022","journal-title":"Am J Cancer Res."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0115","doi-asserted-by":"crossref","first-page":"292","DOI":"10.1159\/000343782","article-title":"The p. G146A and p. P125P polymorphisms in the steroidogenic factor-1 (SF-1) gene do not affect the risk for hypospadias in Caucasians","volume":"6","author":"Adamovic","year":"2012","journal-title":"Sex Dev."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0120","doi-asserted-by":"crossref","first-page":"40","DOI":"10.1038\/aja.2011.67","article-title":"Genetic causes of spermatogenic failure","volume":"14","author":"Massart","year":"2012","journal-title":"Asian J Androl."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0125","doi-asserted-by":"crossref","first-page":"418","DOI":"10.1093\/humrep\/det454","article-title":"The CatSper calcium channel in human sperm: relation with motility and involvement in progesterone-induced acrosome reaction","volume":"29","author":"Tamburrino","year":"2014","journal-title":"Hum Reprod."},{"issue":"Suppl 10","key":"10.1016\/j.acuroe.2023.10.001_bib0130","first-page":"68","article-title":"Non-syndromic monogenic female infertility","volume":"90","author":"Guerri","year":"2019","journal-title":"Acta Biomed."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0135","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1038\/ng0895-383","article-title":"Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA\u2013binding protein gene","volume":"10","author":"Reijo","year":"1995","journal-title":"Nat Genet."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0140","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1210\/mend.15.1.0586","article-title":"Targeted disruption of luteinizing hormone\/human chorionic gonadotropin receptor gene","volume":"15","author":"Lei","year":"2001","journal-title":"Mol Endocrinol."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0145","doi-asserted-by":"crossref","first-page":"172","DOI":"10.1210\/mend.15.1.0582","article-title":"Normal prenatal but arrested postnatal sexual development of luteinizing hormone receptor knockout (LuRKO) mice","volume":"15","author":"Zhang","year":"2001","journal-title":"Mol Endocrinol."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0150","first-page":"1","article-title":"Polymorphism in the alternative donor site of the cryptic exon of lhcgr: functional consequences and associations with testosterone level","volume":"7","author":"Liu","year":"2017","journal-title":"Sci Rep."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0155","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1097\/FPC.0b013e3282f4e98c","article-title":"Polymorphisms of the luteinizing hormone\/chorionic gonadotropin receptor gene: association with maldescended testes and male infertility","volume":"18","author":"Simoni","year":"2008","journal-title":"Pharmacogenet Genomics."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0160","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1016\/S1096-7192(02)00032-X","article-title":"The role of SF1 in adrenal and reproductive function: insight from naturally occurring mutations in humans","volume":"76","author":"Ozisik","year":"2002","journal-title":"Mol Genet Metab."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0165","doi-asserted-by":"crossref","first-page":"395","DOI":"10.1111\/and.12274","article-title":"Mutational screening of the NR5A1 in azoospermia","volume":"47","author":"Zare-Abdollahi","year":"2015","journal-title":"Andrologia."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0170","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1016\/j.fertnstert.2015.04.017","article-title":"Mutational screening of NR5A1 gene encoding steroidogenic factor 1 in cryptorchidism and male factor infertility and functional analysis of seven undescribed mutations","volume":"104","author":"Ferlin","year":"2015","journal-title":"Fertil Steril."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0175","doi-asserted-by":"crossref","first-page":"1012","DOI":"10.1038\/ejhg.2012.290","article-title":"Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males","volume":"21","author":"R\u00f6pke","year":"2013","journal-title":"Eur J Hum Genet."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0180","doi-asserted-by":"crossref","DOI":"10.1111\/and.12931","article-title":"NR 5A1 mutations are not associated with male infertility in Indian men","volume":"50","author":"Sudhakar","year":"2018","journal-title":"Andrologia."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0185","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1007\/s13631-017-0145-y","article-title":"The effects of Factor II (rs1799963) polymorphism on recurrent pregnancy loss in Iranian Azeri women","volume":"13","author":"Isazadeh","year":"2017","journal-title":"Riv Ital Med Lab."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0190","first-page":"671","article-title":"Association of rs1946518 C\/A polymorphism in promoter region of interleukin 18 gene and breast cancer risk in Iranian women: a case-control study","volume":"18","author":"Maroufi","year":"2019","journal-title":"Iran J Allergy Asthma Immunol."},{"key":"10.1016\/j.acuroe.2023.10.001_bib0195","doi-asserted-by":"crossref","DOI":"10.1016\/j.prp.2023.154528","article-title":"Cytokine sustained delivery for cancer therapy; special focus on stem cell-and biomaterial-based delivery methods","author":"Mehralizadeh","year":"2023","journal-title":"Pathol Res Pract."}],"container-title":["Actas Urol\u00f3gicas Espa\u00f1olas (English Edition)"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2173578623001129?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2173578623001129?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,4,1]],"date-time":"2024-04-01T19:01:56Z","timestamp":1711998116000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2173578623001129"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,4]]},"references-count":39,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2024,4]]}},"alternative-id":["S2173578623001129"],"URL":"https:\/\/doi.org\/10.1016\/j.acuroe.2023.10.001","relation":{},"ISSN":["2173-5786"],"issn-type":[{"value":"2173-5786","type":"print"}],"subject":[],"published":{"date-parts":[[2024,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Correlation between LHCGR and NR5A1 genes polymorphism and male infertility risk","name":"articletitle","label":"Article Title"},{"value":"Actas Urol\u00f3gicas Espa\u00f1olas (English Edition)","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.acuroe.2023.10.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"https:\/\/doi.org\/10.1016\/j.acuro.2023.08.002","name":"associatedlink","label":"CrossRef DOI link to the associated document"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 AEU. Published by Elsevier Espa\u00f1a, S.L.U. All rights reserved.","name":"copyright","label":"Copyright"}]}}