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Molecular Human Reproduction|July 8, 2011
A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosisMariem Ben Khelifa, Raoudha Zouari, Radu Harbuz, et al.
Basic and Clinical Andrology|July 25, 2019
Step-by-step loupes-mTESE in non-obstructive azoospermic men, a retrospective studyAmin Bouker, Lazhar Halouani, Mahmoud Kharouf, et al.
La Tunisie Medicale|June 18, 2020
Tunisian Recommendations for resumption of Reproductive Medicine activity in the Covid-19 pandemicMarouen Braham, Mohamed Khrouf, Kais Chaabene, et al.
Human Reproduction (Oxford, England)|April 21, 2016
Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injectionClémentine Wambergue, Raoudha Zouari, Selima Fourati Ben Mustapha, et al.
Human Molecular Genetics|January 2, 2016
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWPJessica Escoffier, Hoi Chang Lee, Sandra Yassine, et al.
American Journal of Human Genetics|March 15, 2011
A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formationRadu Harbuz, Raoudha Zouari, Virginie Pierre, et al.
American Journal of Human Genetics|August 21, 2018
A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male InfertilityZine-Eddine Kherraf, Amir Amiri-Yekta, Denis Dacheux, et al.
EMBO Molecular Medicine|April 18, 2018
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and miceMarie Christou-Kent, Zine-Eddine Kherraf, Amir Amiri-Yekta, et al.
Elife|November 7, 2023
Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum functionDenis Dacheux, Guillaume Martinez, Christine E Broster Reix, et al.
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