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Clinical Genetics|November 17, 2023
CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humansFadwa Jreijiri, Emma Cavarocchi, Amir Amiri-Yekta, et al.
The Journal of Biological Chemistry|December 15, 2015
Progesterone-induced Acrosome Exocytosis Requires Sequential Involvement of Calcium-independent Phospholipase A2β (iPLA2β) and Group X Secreted Phospholipase A2 (sPLA2)Roland Abi Nahed, Guillaume Martinez, Jessica Escoffier, et al.
American Journal of Medical Genetics. Part A|November 7, 2015
Microdeletion del(22)(q12.1) excluding the MN1 gene in a patient with craniofacial anomaliesCaroline Bosson, Françoise Devillard, Véronique Satre, et al.
Asian Journal of Andrology|September 16, 2014
Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian menLeyla Ounis, Abdelali Zoghmar, Charles Coutton, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 1, 1997
Fractures attributable to osteoporosis: report from the National Osteoporosis FoundationL J Melton, M Thamer, N F Ray, et al.
Andrology|January 9, 2025
A recurrent loss-of-function variant in DRC1 causes non-syndromic severe asthenozoospermia with favorable intracytoplasmic sperm injection and pregnancy outcomesCélia Tebbakh, Anne-Laure Barbotin, Guillaume Martinez, et al.
Molecular Human Reproduction|October 31, 2014
Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo developmentSandra Yassine, Jessica Escoffier, Guillaume Martinez, et al.
Molecular Human Reproduction|March 12, 2025
A comprehensive study of the sperm head defects in MMAF condition and their impact on embryo development in miceJana Muroňová, Emeline Lambert, Chanyuth Thamwan, et al.
American Journal of Hypertension|April 8, 2011
Hypertension in response to AT1-AA: role of reactive oxygen species in pregnancy-induced hypertensionMarc R Parrish, Kedra Wallace, Kiran B Tam Tam, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 27, 2021
KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform moleNayeralsadat Fatemi, Pierre F Ray, Fariba Ramezanali, et al.
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