Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Infertility and TAG[original query] |
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Genotyping of Israeli infertile men with idiopathic oligozoospermia. Clinical genetics 2002 Sep 62 (3): 203-7. Madgar I, Green L, Kent-First M, Weissenberg R, Gershoni-Baruch R, Goldman B, Friedman |
Absence of constitutional Y chromosome AZF deletions in patients with testicular germ cell tumors. Urology 2005 1 65 (1): 196-201. Lutke Holzik M F, Storm K, Sijmons R H, D'hollander M, Arts E G J M, Verstraaten M L, Sleijfer D T, Hoekstra H |
Molecular analysis of estrogen receptor alpha gene AGATA haplotype and SNP12 in European populations: potential protective effect for cryptorchidism and lack of association with male infertility. Human reproduction (Oxford, England) 2007 Feb 22 (2): 444-9. Galan J J, Guarducci E, Nuti F, Gonzalez A, Ruiz M, Ruiz A, Krausz |
Functional polymorphism in H2BFWT-5'UTR is associated with susceptibility to male infertility. Journal of cellular and molecular medicine 2009 Jul . Lee J, Park HS, Kim HH, Yun YJ, Lee DR, Lee S |
Association of follicle-stimulating hormone receptor polymorphisms with ovarian response in Chinese women: a prospective clinical study. PloS one 2013 8 (10): e78138. Yan Yuanliang, Gong Zhicheng, Zhang Lu, Li Yanping, Li Xiong, Zhu Lin, Sun Lunqu |
Lack of association of KATNAL1 gene sequence variants and azoospermia in humans. Journal of assisted reproduction and genetics 2014 Aug 31 (8): 1065-71. Fedick Anastasia M, Eckert Kyle, Thompson Katharine, Forman Eric J, Devkota Batsal, Treff Nathan R, Taylor Deanne, Scott Richard |
The Nsun7 (A11337)-deletion mutation, causes reduction of its protein rate and associated with sperm motility defect in infertile men. Journal of assisted reproduction and genetics 2015 May 32 (5): 807-15. Khosronezhad Nahid, Hosseinzadeh Colagar Abasalt, Mortazavi Seyed Mohs |
Is BRD7 associated with spermatogenesis impairment and male infertility in humans? A case-control study in a Han Chinese population. Basic and clinical andrology 2021 9 31 (1): 19. He Tianrong, Liu Mohan, Tao Dachang, Leng Xiangyou, Wang Zhaokun, Xie Shengyu, Zhang Yangwei, Zhang Xinyue, Tan Xiaolan, Liu Yunqiang, Yang Yu |
Suggested role of silent information regulator 1 (SIRT1) gene in female infertility: A cross-sectional study in Pakistan. International journal of clinical practice 2021 Mar e14132. Alam Faiza, Rehman Rehana, Fatima Syeda Sadia, Ashraf Mussarat, Khan Taseer Ahm |
Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia. Frontiers in cell and developmental biology 2023 1 10 1089782. Guzmán-Jiménez Andrea, González-Muñoz Sara, Cerván-Martín Miriam, Rivera-Egea Rocío, Garrido Nicolás, Luján Saturnino, Santos-Ribeiro Samuel, Castilla José A, Gonzalvo M Carmen, Clavero Ana, Vicente F Javier, Maldonado Vicente, Villegas-Salmerón Javier, Burgos Miguel, Jiménez Rafael, Pinto Maria Graça, Pereira Isabel, Nunes Joaquim, Sánchez-Curbelo Josvany, López-Rodrigo Olga, Pereira-Caetano Iris, Marques Patricia Isabel, Carvalho Filipa, Barros Alberto, Bassas Lluís, Seixas Susana, Gonçalves João, Lopes Alexandra M, Larriba Sara, Palomino-Morales Rogelio J, Carmona F David, Bossini-Castillo Lara, , |
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- Page last updated:Apr 22, 2024
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