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

Synchrotron-generated microbeams as a radiosurgical alternative for drug-resistant epilepsies: Proof of concept in a mouse model of mesiotemporal lobe epilepsy

同步加速器产生的微束作为治疗药物难治性癫痫的放射外科替代疗法:在小鼠内侧颞叶癫痫模型中的概念验证

Samalens, Loan; Beets, Camille; Courivaud, Clothilde; Keshmiri, Sarvenaz; Adam, Jean-François; Pellicioli, Paolo; Barbier, Emmanuel Luc; Serduc, Raphaël; Depaulis, Antoine

Comparing Macroscopic and Quantitative Histological Methods to Determine Sexual Maturity in the Female European Plaice, Pleuronectes platessa Linnaeus, 1758

比较宏观组织学方法和定量组织学方法在确定欧洲鲽鱼(Pleuronectes platessa Linnaeus, 1758)雌性性成熟度方面的差异

Sauger, Carine; Quinquis, Jérôme; Kellner, Kristell; Berthelin, Clothilde; Lepoittevin, Mélanie; Elie, Nicolas; Dubroca, Laurent

Two distinct host-specialized fungal species cause white-nose disease in bats

两种不同的、具有宿主特异性的真菌会导致蝙蝠患上白鼻病。

Fischer, Nicola M; Dumville, Imogen; Nabholz, Benoit; Zhelyazkova, Violeta; Stecker, Ruth-Marie; Blomberg, Anna S; Dool, Serena E; Fritze, Marcus; Tilak, Marie-Ka; Bashta, Andriy-Taras; Chenal, Clothilde; Fiston-Lavier, Anna-Sophie; Puechmaille, Sebastien J

Heterochromatic gene silencing controls CD4+ T cell susceptibility to regulatory T cell-mediated suppression in a murine allograft model

异染色质基因沉默控制小鼠同种异体移植模型中 CD4+ T 细胞对调节性 T 细胞介导抑制的敏感性

Julie Noguerol, Karl Laviolette #, Margot Zahm #, Adeline Chaubet, Ambrine Sahal, Claire Détraves, Romain Torres, Clothilde Demont, Véronique Adoue, Carine Joffre, Florence Cammas, Joost Pm van Meerwijk, Olivier P Joffre

Optimized chemical structure extends silencing duration of therapeutic siRNAs in dividing cancer and immune cells

优化的化学结构延长了治疗性siRNA在分裂的癌细胞和免疫细胞中的沉默持续时间。

Kremer, Anastasia; Ryaykenen, Tatyana; Segarra-Visent, Xavier; Sauer, Melanie; Breuer, Leon; Wu, Yiying; Tang, Qi; Cooper, David A; Echeverria, Dimas; Philouze, Clothilde; Bayon, Emilie; Georgess, Dan; Haraszti, Reka A

Genome sequencing for the diagnosis of intellectual disability as a paradigm for rare diseases in the French healthcare setting: the prospective DEFIDIAG study

在法国医疗保健体系中,以基因组测序诊断智力障碍作为罕见病诊断的范例:前瞻性 DEFIDIAG 研究

El Chehadeh, Salima; Heide, Solveig; Quélin, Chloé; Rio, Marlène; Margot, Henri; Geneviève, David; Isidor, Bertrand; Goldenberg, Alice; Guégan, Caroline; Lesca, Gaëtan; Willems, Marjolaine; Ormières, Clothilde; Caumes, Roseline; Busa, Tiffany; Bonneau, Dominique; Guerrot, Anne-Marie; Marey, Isabelle; Vera, Gabriella; Marzin, Pauline; Philippe, Anaïs; Garde, Aurore; Coubes, Christine; Vincent, Marie; Michaud, Vincent; Mignot, Cyril; Charles, Perrine; Sigaudy, Sabine; Edery, Patrick; Lacombe, Didier; Boland, Anne; Nowak, Frédérique; Bouctot, Marion; Humbert-Asensio, Marie-Laure; Simon, Alban; Chennen, Kirsley; Sabour, Niki; Delmas, Christelle; Nicolas, Gaël; Saugier-Veber, Pascale; Lecoquierre, François; Cassinari, Kévin; Keren, Boris; Courtin, Thomas; De Sainte Agathe, Jean-Madeleine; Malan, Valérie; Barcia, Giulia; Tran Mau-Them, Frédéric; Safraou, Hana; Philippe, Christophe; Thévenon, Julien; Chatron, Nicolas; Januel, Louis; Piton, Amélie; Haushalter, Virginie; Gérard, Bénédicte; Lejeune, Catherine; Faivre, Laurence; Sanlaville, Damien; Héron, Delphine; Odent, Sylvie; Nitschké, Patrick; Schluth-Bolard, Caroline; Lyonnet, Stanislas; Deleuze, Jean-François; Binquet, Christine; Dollfus, Hélène

Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability

UBR5基因杂合变异会导致一种神经发育综合征,表现为发育迟缓、自闭症和智力障碍。

Sabeh, Pascale; Dumas, Samantha A; Maios, Claudia; Daghar, Hiba; Korzeniowski, Marek; Rousseau, Justine; Lines, Matthew; Guerin, Andrea; Millichap, John J; Landsverk, Megan; Grebe, Theresa; Lindstrom, Kristin; Strober, Jonathan; Ait Mouhoub, Tarik; Zweier, Christiane; Steinraths, Michelle; Hebebrand, Moritz; Callewaert, Bert; Abou Jamra, Rami; Kautza-Lucht, Monika; Wegler, Meret; Kruszka, Paul; Kumps, Candy; Banne, Ehud; Waberski, Marta Biderman; Dieux, Anne; Raible, Sarah; Krantz, Ian; Medne, Livija; Pechter, Kieran; Villard, Laurent; Guerrini, Renzo; Bianchini, Claudia; Barba, Carmen; Mei, Davide; Blanc, Xavier; Kallay, Christine; Ranza, Emmanuelle; Yang, Xiao-Ru; O'Heir, Emily; Donald, Kirsten A; Murugasen, Serini; Bruwer, Zandre; Calikoglu, Muge; Mathews, Jennifer M; Lesieur-Sebellin, Marion; Baujat, Geneviève; Derive, Nicolas; Pierson, Tyler Mark; Murrell, Jill R; Shillington, Amelle; Ormieres, Clothilde; Rondeau, Sophie; Reis, André; Fernandez-Jaen, Alberto; Au, Ping Yee Billie; Sweetser, David A; Briere, Lauren C; Couque, Nathalie; Perrin, Laurence; Schymick, Jennifer; Gueguen, Paul; Lefebvre, Mathilde; Van Andel, Michael; Juusola, Jane; Antonarakis, Stylianos E; Parker, J Alex; Burnett, Barrington G; Campeau, Philippe M

Comorbidities in the mouse model of temporal lobe epilepsy induced by intrahippocampal kainate

海马内注射红藻氨酸诱导颞叶癫痫小鼠模型中的合并症

Samalens, Loan; Beets, Camille; Courivaud, Clothilde; Kahane, Philippe; Depaulis, Antoine

Case Report: Necrotizing granulomas in the central nervous system: sarcoidosis masquerading as neurotuberculosis

病例报告:中枢神经系统坏死性肉芽肿:结节病伪装成神经结核

Gros, Clothilde; Hankiewicz, Karolina; Carle, Adrien; Cazals-Hatem, Dominique; Bonnan, Mickael

Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech

揭示无智力障碍、自闭症或言语失用症儿童发育性语言障碍的遗传基础

Ormieres, Clothilde; Lesieur-Sebellin, Marion; Siquier-Pernet, Karine; Delplancq, Geoffroy; Rio, Marlene; Parisot, Mélanie; Nitschké, Patrick; Rodriguez-Fontenla, Cristina; Bodineau, Alison; Narcy, Lucie; Schlumberger, Emilie; Cantagrel, Vincent; Malan, Valérie