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

Sepsis-induced NET formation requires MYD88 but is independent of GSDMD and PAD4

脓毒症诱导的 NET 形成需要 MYD88,但与 GSDMD 和 PAD4 无关

Hanna Englert, Chandini Rangaswamy, Giuliano A Kullik, Mylène Divivier, Josephine Göbel, Irm Hermans-Borgmeyer, Uwe Borgmeyer, Kerri A Mowen, Manu Beerens, Maike Frye, Reiner K Mailer, Mathias Gelderblom, Evi X Stavrou, Roger J S Preston, Stefan W Schneider, Tobias A Fuchs, Thomas Renné1

Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosis

多发性硬化症期间 CD99 对 T 细胞共刺激的性别和物种特异性贡献

Ingo Winschel, Anne Willing, Jan Broder Engler, Mark Walkenhorst, Nina Meurs, Lars Binkle-Ladisch, Marcel S Woo, Lena Kristina Pfeffer, Jana K Sonner, Uwe Borgmeyer, Sven Hendrik Hagen, Benjamin Grünhagel, Janna M Claussen, Marcus Altfeld, Manuel A Friese

Lack of a protective effect of the Tmem106b "protective SNP" in the Grn knockout mouse model for frontotemporal lobar degeneration

Grn 基因敲除小鼠模型中 Tmem106b“保护性 SNP”对额颞叶变性缺乏保护作用

Anne-Sophie Cabron, Uwe Borgmeyer, Julia Richter, Helga Peisker, Katharina Gutbrod, Peter Dörmann, Anja Capell, Markus Damme

The adaptor protein PICK1 targets the sorting receptor SorLA

衔接蛋白 PICK1 靶向分选受体 SorLA

Lars Binkle, Marcel Klein, Uwe Borgmeyer, Dietmar Kuhl, Guido Hermey

Revisiting the proteolytic processing of cell adhesion molecule L1

重新审视细胞粘附分子L1的蛋白水解加工

Ralf Kleene, David Lutz, Gabriele Loers, Ute Bork, Uwe Borgmeyer, Irm Hermans-Borgmeyer, Melitta Schachner

A variant in IL6ST with a selective IL-11 signaling defect in human and mouse

IL6ST 中的一种变体,在人类和小鼠中存在选择性 IL-11 信号传导缺陷

Tobias Schwerd #, Freia Krause #, Stephen R F Twigg #, Dominik Aschenbrenner, Yin-Huai Chen, Uwe Borgmeyer, Miryam Müller, Santiago Manrique, Neele Schumacher, Steven A Wall, Jonathan Jung, Timo Damm, Claus-Christian Glüer, Jürgen Scheller, Stefan Rose-John, E Yvonne Jones, Arian Laurence, Andrew O

A multiple sclerosis-associated variant of CBLB links genetic risk with type I IFN function

多发性硬化症相关的 CBLB 变体将遗传风险与 I 型 IFN 功能联系起来

Klarissa Hanja Stürner, Uwe Borgmeyer, Christian Schulze, Ole Pless, Roland Martin