JE
Escoffier Breancon, Jessica
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse | 2024 | 52 | 27 | ||||
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse | eLife | 2024 | 26 | 11 | |||
Pantoprazole, a proton-pump inhibitor, impairs human sperm motility and capacitation in vitro | Andrology | 2020 | 241 | 0 | |||
Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice | American Journal of Human Genetics | 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 feasibility | Molecular and Cellular Endocrinology | 2018 | 414 | 1 | |||
Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing | Cell Reports | 2018 | 404 | 195 | |||
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human | Nature Communications | 2018 | 423 | 351 | |||
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice | EMBO Molecular Medicine | 2018 | 439 | 0 | |||
Testicular Dysgenesis Syndrome and Long-Lasting Epigenetic Silencing of Mouse Sperm Genes Involved in the Reproductive System after Prenatal Exposure to DEHP | PloS one | 2017 | 634 | 278 | |||
SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes | EMBO Molecular Medicine | 2017 | 433 | 0 | |||
MPC1-like Is a Placental Mammal-specific Mitochondrial Pyruvate Carrier Subunit Expressed in Postmeiotic Male Germ Cells | The Journal of biological chemistry | 2016 | 553 | 234 | |||
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP | Human molecular genetics | 2016 | 503 | 0 |