JE
Escoffier Breancon, Jessica
| 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 |  | 2024 | 98 | 113 | |||
| Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse | eLife | | 2024 | 76 | 122 | ||
| Pantoprazole, a proton-pump inhibitor, impairs human sperm motility and capacitation in vitro | Andrology |  | 2020 | 347 | 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 | 437 | 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 | 452 | 1 | ||
| Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing | Cell Reports | | 2018 | 455 | 329 | ||
| Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human | Nature Communications | | 2018 | 483 | 539 | ||
| PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice | EMBO Molecular Medicine | | 2018 | 607 | 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 | 723 | 320 | ||
| SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes | EMBO Molecular Medicine | | 2017 | 497 | 0 | ||
| MPC1-like Is a Placental Mammal-specific Mitochondrial Pyruvate Carrier Subunit Expressed in Postmeiotic Male Germ Cells | The Journal of biological chemistry | | 2016 | 619 | 296 | ||
| 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 | 566 | 0 |
