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

Water mass specific genes dominate the Southern Ocean microbiome

南大洋微生物组以水团特异性基因为主。

Faure, Emile; Pommellec, Jolann; Noel, Cyril; Cormier, Alexandre; Delpech, Lisa-Marie; Eren, A Murat; Fernandez-Guerra, Antonio; Vanni, Chiara; Fourquez, Marion; Houssais, Marie-Noëlle; Guyet, Ulysse; Da Silva, Corinne; Gavory, Frederick; Perdereau, Aude; Labadie, Karine; Wincker, Patrick; Poulain, Julie; Hassler, Christel; Lin, Yajuan; Cassar, Nicolas; Maignien, Loïs

Blood feeding triggers the terminal differentiation of precursor cells in tick salivary glands

蜱虫吸血会触发其唾液腺前体细胞的终末分化。

Mahmood, Sazzad; Lu, Stephen; Barletta Ferreira, Ana Beatriz; Berger, Markus; Oluwayiose, Oladele A; Schneider, Christine A; Leung, Jacqueline M; Garcia Guizzo, Melina; Zhang, Yixiang; Johnson, Randall; Cormier, Kevin W; Suzuki, Motoshi; Brandes, Nathan T; Cooper, Gwendolyn; Gold, Joshua; Schwarz, Benjamin; Olano, Lisa R; Lack, Justin; Barillas-Mury, Carolina; Ribeiro, José M; Tirloni, Lucas

Aryl hydrocarbon receptor in club cells drives Th17-mediated lung injury following inhalation exposure to environmentally persistent free radicals.

吸入环境持久性自由基后,肺泡细胞中的芳烃受体可驱动 Th17 介导的肺损伤。

Pathak Rashmi, Kumar Avinash, Ferrier Ashley, Burk David, Cormier Stephania A

Identification of an episignature for CHD3-related Snijders Blok-Campeau syndrome reveals heterogeneity in the CHARGE syndrome episignature: towards a better characterisation of chromatinopathies

CHD3相关Snijders-Blok-Campeau综合征表观遗传特征的鉴定揭示了CHARGE综合征表观遗传特征的异质性:朝着更好地表征染色质病变迈进

Santini, Amandine; Tognon, Angelo; Richard, Anne-Claire; Velasco, Guillaume; Phan, Gilles; Marzin, Pauline; Maury, Fabien; May, Angele; Michot, Caroline; Chirita-Emandi, Adela; Saraiva, Jorge M; Ballesta-Martinez, Maria Juliana; Lyonnet, Stanislas; Sansović, Ivona; Barakat, Tahsin Stefan; Brunelle, Perrine; Ghoumid, Jamal; Le Guillou, Xavier; Le Tanno, Pauline; Willems, Marjolaine; Zenker, Martin; Schanze, Ina; Moortgat, Stéphanie; Isidor, Bertrand; Paulet, Alix; Yeung, Alison; Levy, Jonathan; Ruscitti, Federica; Pias-Peleteiro, Leticia; Rio, Marlène; Courtin, Thomas; Abdallah, Hamza Hadj; Ducreux, Stéphanie; Laloy, Jean-Sérène; Rollier, Paul; Guerrot, Anne-Marie; Chatron, Nicolas; Demurger, Florence; Goldenberg, Alice; Delanne, Julian; Faivre, Laurence; Lecoquierre, François; Nicolas, Gaël; Coussement, Aurélie; Collet, Corinne; Herenger, Yvan; Defrance, Matthieu; Cormier-Daire, Valérie; Charbonnier, Camille; de Dieuleveult, Maud

A practical guide to unbinned unfolding

一本关于非分类展开的实用指南

Canelli, Florencia; Cormier, Kyle; Cudd, Andrew; Gillberg, Dag; Huang, Roger G; Jin, Weijie; Lee, Sookhyun; Mikuni, Vinicius; Miller, Laura; Nachman, Benjamin; Pan, Jingjing; Pani, Tanmay; Pettee, Mariel; Song, Youqi; Acosta, Fernando Torales

Comparison of short-term complications after open, laparoscopic and robot-assisted radical prostatectomy

开放式、腹腔镜式和机器人辅助式根治性前列腺切除术后短期并发症的比较

Nunes, Prescillia; Richaud, François; Quantin, Catherine; Binquet, Christine; Cormier, Luc; Mariet, Anne-Sophie

A rare coexistence: Ollier disease and primary hyperparathyroidism-mere coincidence or expanding the spectrum of Ollier disease?

罕见的共存:奥利尔病和原发性甲状旁腺功能亢进症——仅仅是巧合还是奥利尔病谱的扩大?

Luciano, Justine; Dauchez, Astrid; Cochand-Priollet, Beatrix; Ginguay, Antonin; Melot, Charlotte; Michot, Caroline; Nizard, Mevyn; Monnot, Sophie; Sailhan, Frédéric; Cormier-Daire, Valérie; Koumakis, Eugénie

Examining social camouflaging and its cognitive, mental health and neurophysiological correlates in autistic adolescents through triangulation-based assessment using self, parent and daily diary reports: a study protocol

通过基于三角测量法的评估,结合自我报告、父母报告和日常日记报告,探讨自闭症青少年社交伪装及其认知、心理健康和神经生理相关性:一项研究方案

Klein, Jessica; Krahn, Rachel L; Howe, Stephanie J; Cormier, Allison; Rush, Jonathan; Ames, Megan; McMorris, Carly A; Macoun, Sarah

Experience With Brivaracetam in the Acute Care Setting at a Large Tertiary Care Center

在大型三级医疗中心急性护理环境中应用布瓦西坦的经验

Cormier, Justine; Traner, Christopher; Subramaniam, Thanujaa; Garcia, Gabriella; Hirsch, Lawrence J; Ammar, Abdalla A; Gilmore, Emily J

A missing enzyme-rescue metabolite as cause of a rare skeletal dysplasia

缺失的酶拯救代谢物是导致罕见骨骼发育不良的原因

Jean Jacobs #,Hristiana Lyubenova #,Sven Potelle,Johannes Kopp ,Isabelle Gerin,Wing Lee Chan,Miguel Rodriguez de Los Santos ,Wiebke Hülsemann,Martin A Mensah ,Valérie Cormier-Daire,Marieke Joosten,Hennie T Bruggenwirth,Kyra E Stuurman,Valancy Miranda,Philippe M Campeau,Lars Wittler,Julie Graff,Stefan Mundlos ,Daniel M Ibrahim,Emile Van Schaftingen,Björn Fischer-Zirnsak ,Uwe Kornak,Nadja Ehmke ,Guido T Bommer  0