日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in "Blonde d'Aquitaine" calves

EGFR基因中的一种常染色体隐性无义变异会导致“阿基坦金发牛”小牛围产期死亡。

Floriot, Sandrine; Fritz, Sébastien; Herry, Vincent; Beauvallet, Christian; Boussaha, Mekki; Egidy, Giorgia; Duchesne, Amandine; Vilotte, Marthe; Cadiergues, Marie-Christine; Boichard, Didier; Schelcher, François; Vilotte, Jean-Luc

Overexpression of the STOX1B isoform of STOX1 triggers preeclampsia-like symptoms through HNF4α-dependent alterations of coagulation cascades in mice

STOX1B亚型的过度表达可通过HNF4α依赖性的凝血级联反应改变,在小鼠体内引发类似先兆子痫的症状。

Collinot, Hélène; Strubé, Louise; Benouda, Ikram; Castille, Johan; Floriot, Sandrine; Daniel-Carlier, Nathalie; Passet, Bruno; Lager, Franck; Lagoutte, Isabelle; Renault, Gilles; Saintpierre, Benjamin; Favier, Maryline; Djeridane, Djihane; Méhats, Céline; Miralles, Francisco; Vilotte, Jean-Luc; Vaiman, Daniel

CRISPR/Cas9-editing of PRNP in Alpine goats

利用 CRISPR/Cas9 技术编辑高山山羊的 PRNP 基因

Allais-Bonnet, Aurélie; Richard, Christophe; André, Marjolaine; Gelin, Valérie; Deloche, Marie-Christine; Lamadon, Aurore; Morin, Gwendoline; Mandon-Pépin, Béatrice; Canon, Eugénie; Thépot, Dominique; Laubier, Johann; Moazami-Goudarzi, Katayoun; Laffont, Ludivine; Dubois, Olivier; Fassier, Thierry; Congar, Patrice; Lasserre, Olivier; Aguirre-Lavin, Tiphaine; Vilotte, Jean-Luc; Pailhoux, Eric

Improving laboratory animal genetic reporting: LAG-R guidelines

改进实验动物遗传报告:LAG-R 指南

Teboul, Lydia; Amos-Landgraf, James; Benavides, Fernando J; Birling, Marie-Christine; Brown, Steve D M; Bryda, Elizabeth; Bunton-Stasyshyn, Rosie; Chin, Hsian-Jean; Crispo, Martina; Delerue, Fabien; Dobbie, Michael; Franklin, Craig L; Fuchtbauer, Ernst-Martin; Gao, Xiang; Golzio, Christelle; Haffner, Rebecca; Hérault, Yann; Hrabe de Angelis, Martin; Lloyd, Kevin C Kent; Magnuson, Terry R; Montoliu, Lluis; Murray, Stephen A; Nam, Ki-Hoan; Nutter, Lauryl M J; Pailhoux, Eric; Pardo Manuel de Villena, Fernando; Peterson, Kevin; Reinholdt, Laura; Sedlacek, Radislav; Seong, Je Kyung; Shiroishi, Toshihiko; Smith, Cynthia; Takeo, Toru; Tinsley, Louise; Vilotte, Jean-Luc; Warming, Søren; Wells, Sara; Whitelaw, C Bruce; Yoshiki, Atsushi; Pavlovic, Guillaume

Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.

小鼠先天性小角膜缺失将 Sox21 失调与疾病联系起来,并表明 TGFB2 在青光眼和近视中发挥作用

Erjavec Elisa, Angée Clémentine, Hadjadj Djihad, Passet Bruno, David Pierre, Kostic Corinne, Dodé Emmanuel, Zanlonghi Xavier, Cagnard Nicolas, Nedelec Brigitte, Crippa Sylvain V, Bole-Feysot Christine, Zarhrate Mohammed, Creuzet Sophie, Castille Johan, Vilotte Jean-Luc, Calvas Patrick, Plaisancié Julie, Chassaing Nicolas, Kaplan Josseline, Rozet Jean-Michel, Fares Taie L

Wnt, glucocorticoid and cellular prion protein cooperate to drive a mesenchymal phenotype with poor prognosis in colon cancer

Wnt信号通路、糖皮质激素和细胞朊蛋白协同作用,驱动结肠癌细胞向间质表型转化,导致预后不良。

Mouillet-Richard, Sophie; Gougelet, Angélique; Passet, Bruno; Brochard, Camille; Le Corre, Delphine; Pitasi, Caterina Luana; Joubel, Camille; Sroussi, Marine; Gallois, Claire; Lavergne, Julien; Castille, Johan; Vilotte, Marthe; Daniel-Carlier, Nathalie; Pilati, Camilla; de Reyniès, Aurélien; Djouadi, Fatima; Colnot, Sabine; André, Thierry; Taieb, Julien; Vilotte, Jean-Luc; Romagnolo, Béatrice; Laurent-Puig, Pierre

Variation in the prion protein gene (PRNP) open reading frame sequence in French cervids

法国鹿科动物朊病毒蛋白基因(PRNP)开放阅读框序列的变异

Laubier, Johann; Van De Wiele, Anne; Barboiron, Aurélie; Laloë, Denis; Saint-Andrieux, Christine; Castille, Johan; Meloni, Emma; Ernst, Sonja; Pellerin, Maryline; Floriot, Sandrine; Daniel-Carlier, Nathalie; Passet, Bruno; Merlet, Joël; Verheyden, Hélène; Béringue, Vincent; Andréoletti, Olivier; Houston, Fiona; Vilotte, Jean-Luc; Bourret, Vincent; Moazami-Goudarzi, Katayoun

Potential genetic robustness of Prnp and Sprn double knockout mouse embryos towards ShRNA-lentiviral inoculation

Prnp和Sprn双敲除小鼠胚胎对shRNA慢病毒接种的潜在遗传稳健性

Rau, Andrea; Passet, Bruno; Castille, Johan; Daniel-Carlier, Nathalie; Asset, Alexandre; Lecardonnel, Jérome; Moroldo, Marco; Jaffrézic, Florence; Laloë, Denis; Moazami-Goudarzi, Katayoun; Vilotte, Jean-Luc

Cellular prion protein dysfunction in a prototypical inherited metabolic myopathy

典型遗传性代谢性肌病中的细胞朊蛋白功能障碍

Boufroura, Fatima-Zohra; Tomkiewicz-Raulet, Céline; Poindessous, Virginie; Castille, Johan; Vilotte, Jean-Luc; Bastin, Jean; Mouillet-Richard, Sophie; Djouadi, Fatima

Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients

与法国和英国接受人类生长激素治疗者相关的医源性克雅氏病朊病毒株

Douet, Jean-Yves; Huor, Alvina; Cassard, Hervé; Lugan, Séverine; Aron, Naïma; Mesic, Chloé; Vilette, Didier; Barrio, Tomás; Streichenberger, Nathalie; Perret-Liaudet, Armand; Delisle, Marie-Bernadette; Péran, Patrice; Deslys, Jean-Philippe; Comoy, Emmanuel; Vilotte, Jean-Luc; Goudarzi, Katayoun; Béringue, Vincent; Barria, Marcelo A; Ritchie, Diane L; Ironside, James W; Andréoletti, Olivier