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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Springe zu: 2021 | 2020 | 2019 | 2017
Anzahl der Publikationen: 4

2021

Wang, Lin; Aschenbrenner, Dominik; Zeng, Zhiyang; Cao, Xiya; Mayr, Daniel; Mehta, Meera; Capitani, Melania; Warner, Neil; Pan, Jie; Wang, Liren; Li, Qi; Zuo, Tao; Cohen-Kedar, Sarit; Lu, Jiawei; Ardy, Rico Chandra; Mulder, Daniel J.; Dissanayake, Dilan; Peng, Kaiyue; Huang, Zhiheng; Li, Xiaoqin; Wang, Yuesheng; Wang, Xiaobing; Li, Shuchao; Bullers, Samuel; Gammage, Anis N.; Warnatz, Klaus; Schiefer, Ana-Iris; Krivan, Gergely; Goda, Vera; Kahr, Walter H. A.; Lemaire, Mathieu; Lu, Chien-Yi; Siddiqui, Iram; Surette, Michael G.; Kotlarz, Daniel; Engelhardt, Karin R.; Griffin, Helen R.; Rottapel, Robert; Decaluwe, Helene; Laxer, Ronald M.; Proietti, Michele; Hambleton, Sophie; Elcombe, Suzanne; Guo, Cong-Hui; Grimbacher, Bodo; Dotan, Iris; Ng, Siew C.; Freeman, Spencer A.; Snapper, Scott B.; Klein, Christoph; Boztug, Kaan; Huang, Ying; Li, Dali; Uhlig, Holm H. und Muise, Aleixo M. (2021): Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice. In: Nature Genetics, Bd. 53, Nr. 4: S. 500-510

2020

Schwerd, Tobias; Krause, Freia; Twigg, Stephen R. F.; Aschenbrenner, Dominik; Chen, Yin-Huai; Borgmeyer, Uwe; Müller, Miryam; Manrique, Santiago; Schumacher, Neele; Wall, Steven A.; Jung, Jonathan; Damm, Timo; Glueer, Claus-Christian; Scheller, Jürgen; Rose-John, Stefan; Jones, E. Yvonne; Laurence, Arian; Wilkie, Andrew O. M.; Schmidt-Arras, Dirk und Uhlig, Holm H. (2020): A variant in IL6ST with a selective IL-11 signaling defect in human and mouse. In: Bone Research, Bd. 8, Nr. 1, 24

2019

Shahin, Tala; Aschenbrenner, Dominik; Cagdas, Deniz; Bal, Sevgi Koestel; Conde, Cecilia Dominguez; Garncarz, Wojciech; Medgyesi, David; Schwerd, Tobias; Karaatmaca, Betul; Cetinkaya, Pinar Gur; Esenboga, Saliha; Twigg, Stephen R. F.; Cant, Andrew; Wilkie, Andrew O. M.; Tezcan, Ilhan; Uhlig, Holm H. und Boztug, Kaan (2019): Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function. In: Haematologica, Bd. 104, Nr. 3: S. 609-621

2017

Schwerd, Tobias; Twigg, Stephen R. F.; Aschenbrenner, Dominik; Manrique, Santiago; Miller, Kerry A.; Taylor, Indira B.; Capitani, Melania; McGowan, Simon J.; Sweeney, Elizabeth; Weber, Astrid; Chen, Liye; Bowness, Paul; Riordan, Andrew; Cant, Andrew; Freeman, Alexandra F.; Milner, Joshua D.; Holland, Steven M.; Frede, Natalie; Müller, Miryam; Schmidt-Arras, Dirk; Grimbacher, Bodo; Wall, Steven A.; Jones, E. Yvonne; Wilkie, Andrew O. M. und Uhlig, Holm H. (2017): A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis. In: Journal of Experimental Medicine, Bd. 214, Nr. 9: S. 2547-2562

Diese Liste wurde am Sat Mar 23 23:04:46 2024 CET erstellt.