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

Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers

更正:显性负性ADA2突变会导致杂合子携带者出现ADA2缺乏症。

Wouters, Marjon; Ehlers, Lisa; Van Eynde, Wout; Kars, Meltem Ece; Delafontaine, Selket; Kienapfel, Verena; Dzhus, Mariia; Schrijvers, Rik; De Haes, Petra; Struyf, Sofie; Bucciol, Giorgia; Itan, Yuval; Bolze, Alexandre; Voet, Arnout; Hombrouck, Anneleen; Moens, Leen; Ogunjimi, Benson; Meyts, Isabelle

Blood Pressure Trajectory From Birth to Preschool and School Age in the ENVIRONAGE Birth Cohort

环境出生队列中从出生到学龄前和学龄期的血压变化轨迹

Yu, Yu-Ling; Renaers, Eleni; Martens, Dries S; Sleurs, Hanne; Massot, Anneleen; Berden, Daphne; Verheyen, Lore; Alfano, Rossella; Zhang, Dong-Yan; An, De-Wei; Raaijmakers, Anke; Allegaert, Karel; Verhamme, Peter; Plusquin, Michelle; Staessen, Jan A; Nawrot, Tim S

ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances.

ADA2 缺陷细胞表现出细胞死亡水平升高和代谢紊乱。

Ehlers Lisa, Wouters Marjon, Pillay Bethany, Delafontaine Selket, Bucciol Giorgia, Baggio Marco, Dzhus Mariia, Hombrouck Anneleen, Damerau Alexandra, De Somer Lien, Schrijvers Rik, Vanderschueren Steven, Jacquemyn Maarten, Kallinich Tilmann, Daelemans Dirk, Ghesquière Bart, Agostinis Patrizia, Moens Leen, Meyts Isabelle

Time and patient journey to axial spondyloarthritis diagnosis: a retrospective study in French primary care

中轴型脊柱关节炎诊断的时间和患者就诊历程:一项法国基层医疗回顾性研究

Prati, Clément; Constantin, Arnaud; Dernis, Emmanuelle; Gottenberg, Jacques Eric; Rozenblat, Marc; Arnee, Elise; Ducros, Marie; Tamberou, Cheikh; Vyncke, Anneleen; Gandrup Horan, Julie

High stability of the genome of Akkermansia muciniphila Muc(T) under long-term culturing conditions

在长期培养条件下,Akkermansia muciniphila Muc(T) 基因组具有高度稳定性

Ligthart, Kate; Elzinga, Janneke; Segers, Anneleen; Smidt, Hauke; de Vos, Willem M

Toward automated neonatal EEG analysis: multi-center validation of a reliable deep learning pipeline

迈向新生儿脑电图自动化分析:可靠深度学习流程的多中心验证

Hermans, Tim; Dereymaeker, Anneleen; Lemmens, Katrien; Jansen, Katrien; Usman, Fatima; Robinson, Shellie; Naulaers, Gunnar; De Vos, Maarten; Hartley, Caroline

Sexual harassment protocols at the European universities: An overview of key components and recommendations for improvement

欧洲大学性骚扰应对规程:关键要素概述及改进建议

Berbegal-Bernabeu, Marina; Pérez-Martínez, Vanesa; Sousa, Mafalda; Neves, Sofia; De Cuyper, Anneleen; Porru, Stefano; Carta, Angela; Manchenko, Maryna; Jaskulska, Sylwia; Jankowiak, Barbara; Wallner, Marlies; Stifter, Viktoria; Vives-Cases, Carmen

Human skeletal muscle fiber heterogeneity beyond myosin heavy chains

人类骨骼肌纤维异质性超越肌球蛋白重链

Roger Moreno-Justicia # ,Thibaux Van der Stede # ,Ben Stocks # ,Jenni Laitila ,Robert A Seaborne ,Alexia Van de Loock ,Eline Lievens ,Diana Samodova ,Leyre Marín-Arraiza ,Oksana Dmytriyeva ,Robin Browaeys ,Kim Van Vossel ,Lukas Moesgaard ,Nurten Yigit ,Jasper Anckaert ,Anneleen Weyns ,Ruud Van Thienen ,Ronni E Sahl ,Edmar Zanoteli ,Michael W Lawlor ,Michael Wierer ,Pieter Mestdagh ,Jo Vandesompele ,Julien Ochala ,Morten Hostrup ,Wim Derave ,Atul S Deshmukh

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers

显性负性ADA2突变会导致杂合子携带者出现ADA2缺乏症。

Marjon Wouters,Lisa Ehlers,Wout Van Eynde,Meltem Ece Kars,Selket Delafontaine,Verena Kienapfel,Mariia Dzhus,Rik Schrijvers,Petra De Haes,Sofie Struyf,Giorgia Bucciol,Yuval Itan,Alexandre Bolze,Arnout Voet,Anneleen Hombrouck,Leen Moens,Benson Ogunjimi,Isabelle Meyts

Inhibition of lysosomal degradation increases expression of mutant ADA2 in DADA2 monocytes

抑制溶酶体降解会增加DADA2单核细胞中突变型ADA2的表达。

Ehlers, Lisa; Wouters, Marjon; Pillay, Bethany; Delafontaine, Selket; Dzhus, Mariia; Baggio, Marco; Niehues, Tim; Dückers, Gregor; Sevenants, Lieve; Casteels, Kristina; De Somer, Lien; Schrijvers, Rik; Vanderschueren, Steven; Jacquemyn, Maarten; Daelemans, Dirk; Hombrouck, Anneleen; Chambers, Eugene P; Tousseyn, Thomas; Bucciol, Giorgia; Agostinis, Patrizia; Moens, Leen; Meyts, Isabelle