| Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms B Tesi, J Davidsson, M Voss, E Rahikkala, TD Holmes, SCC Chiang, ... Blood 129 (16), 2266-2279, 2017 | 212 | 2017 |
| Mechanism, specificity, and physiology of signal peptide peptidase (SPP) and SPP-like proteases M Voss, B Schröder, R Fluhrer Biochimica et Biophysica Acta (BBA)-Biomembranes 1828 (12), 2828-2839, 2013 | 182 | 2013 |
| Shedding of glycan‐modifying enzymes by signal peptide peptidase‐like 3 (SPPL3) regulates cellular N‐glycosylation M Voss, U Künzel, F Higel, PH Kuhn, A Colombo, A Fukumori, ... The EMBO journal 33 (24), 2890-2905, 2014 | 114 | 2014 |
| Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7 VB Pastor, S Sahoo, J Boklan, GC Schwabe, E Saribeyoglu, B Strahm, ... Haematologica, haematol. 2017.180778, 2017 | 108 | 2017 |
| Secretome analysis identifies novel signal peptide peptidase-like 3 (SPPL3) substrates and reveals a role of SPPL3 in multiple Golgi glycosylation pathways PH Kuhn, M Voss, M Haug-Kröper, B Schröder, U Schepers, S Bräse, ... Molecular & Cellular Proteomics 14 (6), 1584-1598, 2015 | 98 | 2015 |
| Requirements for leukocyte transmigration via the transmembrane chemokine CX3CL1 N Schwarz, J Pruessmeyer, FM Hess, D Dreymueller, E Pantaler, ... Cellular and molecular life sciences 67 (24), 4233-4248, 2010 | 68 | 2010 |
| Posttranslational regulation of Fas ligand function M Voss, M Lettau, M Paulsen, O Janssen Cell Commun Signal 6 (11), 10.1186, 2008 | 61 | 2008 |
| Foamy virus envelope protein is a substrate for signal peptide peptidase-like 3 (SPPL3) M Voss, A Fukumori, PH Kuhn, U Künzel, B Klier, G Grammer, ... Journal of Biological Chemistry 287 (52), 43401-43409, 2012 | 54 | 2012 |
| Proteolytic Processing of Neuregulin 1 Type III by Three Intramembrane-cleaving Proteases D Fleck, M Voss, B Brankatschk, C Giudici, H Hampel, B Schwenk, ... Journal of Biological Chemistry 291 (1), 318-333, 2016 | 53 | 2016 |
| Inhibition of ADAM17 impairs endothelial cell necroptosis and blocks metastasis J Bolik, F Krause, M Stevanovic, M Gandraß, I Thomsen, SS Schacht, ... Journal of Experimental Medicine 219 (1), e20201039, 2021 | 51 | 2021 |
| The adapter protein Nck: role of individual SH3 and SH2 binding modules for protein interactions in T lymphocytes M Lettau, J Pieper, A Gerneth, B Lengl‐Janßen, M Voss, A Linkermann, ... Protein Science 19 (4), 658-669, 2010 | 50 | 2010 |
| Natural killer cell biology illuminated by primary immunodeficiency syndromes in humans M Voss, YT Bryceson Clinical Immunology, 2015 | 29 | 2015 |
| Identification of SH3 domain interaction partners of human FasL (CD178) by phage display screening M Voss, M Lettau, O Janssen BMC immunology 10 (1), 53, 2009 | 29 | 2009 |
| A RAB27A 5′ untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation B Tesi, J Rascon, SCC Chiang, B Burnyte, A Löfstedt, A Fasth, ... Journal of Allergy and Clinical Immunology 142 (1), 317-321. e8, 2018 | 26 | 2018 |
| N-terminome analyses underscore the prevalence of SPPL3-mediated intramembrane proteolysis among Golgi-resident enzymes and its role in Golgi enzyme secretion L Hobohm, T Koudelka, FH Bahr, J Truberg, S Kapell, SS Schacht, ... Cellular and Molecular Life Sciences 79 (3), 1-23, 2022 | 11 | 2022 |
| Differential protein–protein interactions of full length human FasL and FasL fragments generated by proteolysis M Lettau, M Voss, H Ebsen, D Kabelitz, O Janssen Experimental cell research 320 (2), 290-301, 2014 | 9 | 2014 |
| Alternative UNC13D Promoter Encodes a Functional Munc13-4 Isoform Predominantly Expressed in Lymphocytes and Platelets D Galgano, T Soheili, M Voss, L Torralba-Raga, B Tesi, F Cichocki, ... Frontiers in Immunology 11, 1154, 2020 | 7 | 2020 |
| Endogenous tagging reveals a mid-Golgi localization of the glycosyltransferase-cleaving intramembrane protease SPPL3 J Truberg, L Hobohm, A Jochimsen, C Desel, M Schweizer, M Voss Biochimica et Biophysica Acta (BBA)-Molecular Cell Research, 119345, 2022 | 5 | 2022 |
| Cytopenia, Predisposition to Myelodysplastic Syndrome, Immunodeficiency, and Neurological Disease Caused By Gain-of-Function SAMD9L Mutations Is Frequently Ameliorated By … B Tesi, J Davidsson, M Voss, T Holmes, T Ripperger, S Chiang, L Nilsson, ... Blood 128 (22), 4299-4299, 2016 | 4 | 2016 |
| EGFR stimulation enables IL-6 trans-signalling via iRhom2-dependent ADAM17 activation in mammary epithelial cells N Schumacher, I Thomsen, F Brundert, V Hejret, S Düsterhöft, B Tichý, ... Biochimica et Biophysica Acta (BBA)-Molecular Cell Research, 119489, 2023 | 2 | 2023 |
