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Title Published in Access level OA Policy Year Views Downloads
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse
accessLevelPublic
2024 52 27
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouseeLife
accessLevelPublic
2024 26 11
Pantoprazole, a proton-pump inhibitor, impairs human sperm motility and capacitation in vitroAndrology
accessLevelRestricted
2020 241 0
Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and MiceAmerican Journal of Human Genetics
accessLevelRestricted
2019 384 0
Creation of knock out and knock in mice by CRISPR/Cas9 to validate candidate genes for human male infertility, interest, difficulties and feasibilityMolecular and Cellular Endocrinology
accessLevelRestricted
2018 414 1
Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA SequencingCell Reports
accessLevelPublic
2018 404 195
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and humanNature Communications
accessLevelPublic
2018 423 351
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and miceEMBO Molecular Medicine
accessLevelRestricted
2018 439 0
Testicular Dysgenesis Syndrome and Long-Lasting Epigenetic Silencing of Mouse Sperm Genes Involved in the Reproductive System after Prenatal Exposure to DEHPPloS one
accessLevelPublic
2017 634 278
SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotesEMBO Molecular Medicine
accessLevelRestricted
2017 433 0
MPC1-like Is a Placental Mammal-specific Mitochondrial Pyruvate Carrier Subunit Expressed in Postmeiotic Male Germ CellsThe Journal of biological chemistry
accessLevelPublic
2016 553 234
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWPHuman molecular genetics
2016 503 0
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