Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Infertility and DPY19L2[original query] |
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Assisted oocyte activation overcomes fertilization failure in globozoospermic patients regardless of the DPY19L2 status. Human reproduction (Oxford, England) 2013 Apr 28 (4): 1054-61. Kuentz P, Vanden Meerschaut F, Elinati E, Nasr-Esfahani M H, Gurgan T, Iqbal N, Carré-Pigeon F, Brugnon F, Gitlin S A, Velez de la Calle J, Kilani Z, De Sutter P, Viville |
Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men. Asian journal of andrology 0 17 (1): 68-73. Ounis Leyla, Zoghmar Abdelali, Coutton Charles, Rouabah Leila, Hachemi Maroua, Martinez Delphine, Martinez Guillaume, Bellil Ines, Khelifi Douadi, Arnoult Christophe, Fauré Julien, Benbouhedja Sebti, Rouabah Abdelkader, Ray Pierre |
Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia. Molecular human reproduction 2015 Oct . Ghédir Houda, Ibala-Romdhane Samira, Okutman Ozlem, Viot Géraldine, Saad Ali, Viville Stépha |
Corrigendum to: Deletion of dpy-19 like 2 (DPY19L2) gene is associated with total but not partial globozoospermia. Reproduction, fertility, and development 2020 May 32 (8): 805. Alimohammadi Fatemeh, Ebrahimi Nasab Mahya, Rafaee Alemeh, Hashemi Mehrdad, Totonchi Mehdi, Mohseni Meybodi Anahita, Sadighi Gilani Mohammad Ali, Sabbaghian Marj |
Deletion of dpy-19 like 2 (DPY19L2) gene is associated with total but not partial globozoospermia. Reproduction, fertility, and development 2020 Apr . Alimohammadi Fatemeh, Ebrahimi Nasab Mahya, Rafaee Alemeh, Hashemi Mehrdad, Totonchi Mehdi, Mohseni Meybodi Anahita, Sadighi Gilani Mohammad Ali, Sabbaghian Marj |
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player. Human genetics 2020 Oct . Celse Tristan, Cazin Caroline, Mietton Flore, Martinez Guillaume, Martinez Delphine, Thierry-Mieg Nicolas, Septier Amandine, Guillemain Catherine, Beurois Julie, Clergeau Antoine, Mustapha Selima Fourati Ben, Kharouf Mahmoud, Zoghmar Abdelali, Chargui Ahmed, Papaxanthos Aline, Dorphin Béatrice, Foliguet Bernard, Triki Chema, Sifer Christophe, Lauton Dominique, Tachdjian Gérard, Schuler Gilles, Lejeune Hervé, Puechberty Jacques, Bessonnat Julien, Pasquier Laurent, Mery Lionel, Poulain Marine, Chaabouni Myriam, Sermondade Nathalie, Cabry Rosalie, Benbouhadja Sebti, Veau Ségolène, Frapsauce Cynthia, Mitchell Valérie, Achard Vincent, Satre Veronique, Hennebicq Sylviane, Zouari Raoudha, Arnoult Christophe, Kherraf Zine-Eddine, Coutton Charles, Ray Pierre |
Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Human reproduction (Oxford, England) 2020 1 35 (1): 240-252. Oud M S, Okutman Ö, Hendricks L A J, de Vries P F, Houston B J, Vissers L E L M, O'Bryan M K, Ramos L, Chemes H E, Viville S, Veltman J |
Sequencing of the ZMYND15 gene in a cohort of infertile Chinese men reveals novel mutations in patients with teratozoospermia. Journal of medical genetics 2022 8 . Wen Yuting, Wang Xiang, Zheng Rui, Dai Siyu, Li Jinhui, Yang Yihong, Shen Yi |
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- Page last updated:Apr 22, 2024
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