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Mohammad Karimian, Leila Parvaresh & Mohaddeseh Behjati. (2021) Genetic variations as molecular diagnostic factors for idiopathic male infertility: current knowledge and future perspectives. Expert Review of Molecular Diagnostics 21:11, pages 1191-1210.
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Sidra Qureshi, Jimmaline J. Hardy, Christopher Pombar, Andrea J. Berman, Agnieszka Malcher, Tara Gingrich, Rachel Hvasta, Jannah Kuong, Sarah Munyoki, Kathleen Hwang, Kyle E. Orwig, Jawad Ahmed, Marta Olszewska, Maciej Kurpisz, Donald F. Conrad, Muhammad Jaseem Khan & Alexander N. Yatsenko. (2023) Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure. Frontiers in Genetics 14.
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Bita Aliasghar, Saba Sane, Masoud Sheidai, Fahime Koohdar & Naser Kalhor. (2023) Association study of rs323344 in TEX15 with non-obstructive azoospermia in Iranian population. Genetika ABI Genetika 55:2, pages 689-705.
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Masoud Sheidai, Sogol Allahverdi, Narges Anvari, Somayeh KhameneEivaziEivazi, Mozhgan AlavijehGhandehariGhandehari, Marziyeh GhoreishiSeyedSeyed, Fatemeh Jamshidi, Ghazal Khosravani, Naser Kalhor & Fahimeh Koohdar. (2023) Text-11 snps and neighboring sequences role in causing male infertility in some ethnic groups of Iranian and their potential role in estimating divergence time. Genetika ABI Genetika 55:1, pages 229-244.
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Federico Belladelli, Wade Muncey & Michael L. Eisenberg. (2023) Reproduction as a window for health in men. Fertility and Sterility.
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Andrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, Rocío Rivera-Egea, Nicolás Garrido, Saturnino Luján, Samuel Santos-Ribeiro, José A. Castilla, M. Carmen Gonzalvo, Ana Clavero, F. Javier Vicente, Vicente Maldonado, Javier Villegas-Salmerón, Miguel Burgos, Rafael Jiménez, Maria Graça Pinto, Isabel Pereira, Joaquim Nunes, Josvany Sánchez-Curbelo, Olga López-Rodrigo, Iris Pereira-Caetano, Patricia Isabel Marques, Filipa Carvalho, Alberto Barros, Lluís Bassas, Susana Seixas, João Gonçalves, Alexandra M. Lopes, Sara Larriba, Rogelio J. Palomino-Morales, F. David Carmona & Lara Bossini-Castillo. (2022) Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia. Frontiers in Cell and Developmental Biology 10.
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Mohammadreza Behvarz, Seyyed Ali Rahmani, Elham Siasi Torbati, Shahla Danaei Mehrabad & Maryam Bikhof Torbati. (2022) Association of CATSPER1, SPATA16 and TEX11 genes polymorphism with idiopathic azoospermia and oligospermia risk in Iranian population. BMC Medical Genomics 15:1.
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Jack Wieland, Sarah Buchan, Sioban Sen Gupta & Anna Mantzouratou. (2022) Genomic instability and the link to infertility: A focus on microsatellites and genomic instability syndromes. European Journal of Obstetrics & Gynecology and Reproductive Biology 274, pages 229-237.
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Hamideh Karimi, Parnaz Borjian Boroujeni, Marjan Sabbaghian & Anahita Mohseni Meybodi. (2021) Gene Alterations and Expression Spectrum of NANOS3 in Nonobstructive Azoospermia. Reproductive Sciences 29:1, pages 92-99.
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Hela Bellil, Farah Ghieh, Emeline Hermel, Béatrice Mandon-Pepin & François Vialard. (2021) Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertility. Basic and Clinical Andrology 31:1.
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Priti Singh, Robert Fragoza, Cecilia S. Blengini, Tina N. Tran, Gianno Pannafino, Najla Al-Sweel, Kerry J. Schimenti, Karen Schindler, Eric A. Alani, Haiyuan Yu & John C. Schimenti. (2021) Human MLH1/3 variants causing aneuploidy, pregnancy loss, and premature reproductive aging. Nature Communications 12:1.
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Theresa Schöpp, Ansgar Zoch, Rebecca V. Berrens, Tania Auchynnikava, Yuka Kabayama, Lina Vasiliauskaitė, Juri Rappsilber, Robin C. Allshire & Dónal O’Carroll. (2020) TEX15 is an essential executor of MIWI2-directed transposon DNA methylation and silencing. Nature Communications 11:1.
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Cerván-Martín, Castilla, Palomino-Morales & Carmona. (2020) Genetic Landscape of Nonobstructive Azoospermia and New Perspectives for the Clinic. Journal of Clinical Medicine 9:2, pages 300.
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Xinyan Zhao, Chunlan Mu, Jia Ma, Xiaojing Dai & Haiyan Jiao. (2019) The association of four SNPs in DNA mismatch repair genes with idiopathic male infertility in northwest China. International Journal of Immunogenetics 46:6, pages 451-458.
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Weiqiang Zhu, Jing Du, Qing Chen, Zhaofeng Zhang, Bin Wu, Jianhua Xu, Tianqi Li, Yuan Bi, Huijuan Shi & Runsheng Li. (2019) Association of UHRF1 gene polymorphisms with oligospermia in Chinese males. Journal of Assisted Reproduction and Genetics 36:12, pages 2563-2573.
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Yanwei Sha, Liangkai Zheng, Zhiyong Ji, Libin Mei, Lu Ding, Shaobin Lin, Xu Wang, Xiaoyu Yang & Ping Li. (2018) A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review. BMC Medical Genetics 19:1.
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Hongjie Pan, Xuan Zhang, Hanwei Jiang, Xiaohua Jiang, Liu Wang, Qi Qi, Yuan Bi, Jian Wang, Qinghua Shi & Runsheng Li. (2017) Ndrg3 gene regulates DSB repair during meiosis through modulation the ERK signal pathway in the male germ cells. Scientific Reports 7:1.
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George Anifandis, Ourania Markandona, Konstantinos Dafopoulos, Christina Messini, Aspasia Tsezou, Marina Dimitraki, Panagiotis Georgoulias, Alexandros Daponte & Ioannis Messinis. (2017) Embryological Results of Couples Undergoing ICSI-ET Treatments with Males Carrying the Single Nucleotide Polymorphism rs175080 of the MLH3 Gene. International Journal of Molecular Sciences 18:2, pages 314.
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