Development of an innovative 3D cell culture system to study tumour-stroma interactions in non-small cell lung cancer cells A Amann, M Zwierzina, G Gamerith, M Bitsche, JM Huber, GF Vogel, ... PloS one 9 (3), e92511, 2014 | 219 | 2014 |
Coordinated binding of Vps4 to ESCRT-III drives membrane neck constriction during MVB vesicle formation MAY Adell, GF Vogel, M Pakdel, M Müller, H Lindner, MW Hess, D Teis J Cell Biol 205 (1), 33-49, 2014 | 218 | 2014 |
Loss of syntaxin 3 causes variant microvillus inclusion disease CL Wiegerinck, AR Janecke, K Schneeberger, GF Vogel, ... Gastroenterology 147 (1), 65-68. e10, 2014 | 189 | 2014 |
Recruitment dynamics of ESCRT-III and Vps4 to endosomes and implications for reverse membrane budding MAY Adell, SM Migliano, S Upadhyayula, YS Bykov, S Sprenger, ... Elife 6, e31652, 2017 | 163 | 2017 |
LAMTOR/Ragulator is a negative regulator of Arl8b-and BORC-dependent late endosomal positioning PA Filipek, MEG de Araujo, GF Vogel, CH De Smet, D Eberharter, ... J Cell Biol 216 (12), 4199-4215, 2017 | 114 | 2017 |
Cargo-selective apical exocytosis in epithelial cells is conducted by Myo5B, Slp4a, Vamp7, and Syntaxin 3 GF Vogel, KMC Klee, AR Janecke, T Müller, MW Hess, LA Huber J Cell Biol 211 (3), 587-604, 2015 | 110 | 2015 |
An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral trafficking K Schneeberger, GF Vogel, H Teunissen, DD van Ommen, H Begthel, ... Proceedings of the National Academy of Sciences 112 (40), 12408-12413, 2015 | 89 | 2015 |
Microvillus inclusion disease: loss of myosin Vb disrupts intracellular traffic and cell polarity CE Thoeni, GF Vogel, I Tancevski, S Geley, S Lechner, K Pfaller, ... Traffic 15 (1), 22-42, 2014 | 80 | 2014 |
Abnormal Rab11‐Rab8‐vesicles cluster in enterocytes of patients with microvillus inclusion disease GF Vogel, AR Janecke, IM Krainer, K Gutleben, B Witting, SG Mitton, ... Traffic 18 (7), 453-464, 2017 | 57 | 2017 |
Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations GF Vogel, JM van Rijn, IM Krainer, AR Janecke, C Posovzsky, M Cohen, ... JCI insight 2 (14), 2017 | 56 | 2017 |
Interleukin-like epithelial-to-mesenchymal transition inducer activity is controlled by proteolytic processing and plasminogen–urokinase plasminogen activator receptor system … A Csiszar, B Kutay, S Wirth, U Schmidt, S Macho-Maschler, M Schreiber, ... Breast Cancer Research 16 (5), 433, 2014 | 55 | 2014 |
Efficacy of elimination diets in eosinophilic esophagitis: a systematic review and meta-analysis C Mayerhofer, AM Kavallar, D Aldrian, AK Lindner, T Müller, GF Vogel Clinical Gastroenterology and Hepatology, 2023 | 51 | 2023 |
The haemochromatosis gene Hfe and Kupffer cells control LDL cholesterol homeostasis and impact on atherosclerosis development E Demetz, P Tymoszuk, R Hilbe, C Volani, D Haschka, C Heim, K Auer, ... European Heart Journal, 2020 | 46 | 2020 |
Congenital diarrhea and cholestatic liver disease: Phenotypic spectrum associated with MYO5B mutations D Aldrian, GF Vogel, TK Frey, H Ayyıldız Civan, AÜ Aksu, Y Avitzur, ... Journal of clinical medicine 10 (3), 481, 2021 | 44 | 2021 |
Ultrastructural morphometry points to a new role for LAMTOR2 in regulating the endo/lysosomal system GF Vogel, HL Ebner, MEG de Araujo, T Schmiedinger, O Eiter, H Pircher, ... Traffic 16 (6), 617-634, 2015 | 36 | 2015 |
BORC regulates late endosomal/lysosomal size through PIKfyve‐dependent phosphatidylinositol‐3, 5‐bisphosphate TE Yordanov, VEB Hipolito, G Liebscher, GF Vogel, T Stasyk, C Herrmann, ... Traffic, 0 | 35* | |
AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect. KMC Klee, AR Janecke, HA Civan, Š Rosipal, P Heinz-Erian, LA Huber, ... Human genetics, 2020 | 34 | 2020 |
Biogenesis of lysosome-related organelles complex-1 (BORC) regulates late endosomal/lysosomal size through PIKfyve-dependent phosphatidylinositol-3, 5-bisphosphate. TE Yordanov, VEB Hipolito, G Liebscher, GF Vogel, T Stasyk, C Herrmann, ... Traffic (Copenhagen, Denmark) 20 (9), 674-696, 2019 | 32 | 2019 |
Towards understanding microvillus inclusion disease GF Vogel, MW Hess, K Pfaller, LA Huber, AR Janecke, T Müller Molecular and cellular pediatrics 3 (1), 3, 2016 | 29 | 2016 |
UNC45A deficiency causes microvillus inclusion disease–like phenotype by impairing myosin VB–dependent apical trafficking R Duclaux-Loras, C Lebreton, J Berthelet, F Charbit-Henrion, O Nicolle, ... The Journal of Clinical Investigation 132 (10), 2023 | 22 | 2023 |