Georg Vogel
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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
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
Loss of syntaxin 3 causes variant microvillus inclusion disease
CL Wiegerinck, AR Janecke, K Schneeberger, GF Vogel, ...
Gastroenterology 147 (1), 65-68. e10, 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
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
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
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
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
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
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
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
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
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
Cryo‐immunoelectron microscopy of adherent cells improved by the use of electrospun cell culture substrates
T Schmiedinger, GF Vogel, O Eiter, K Pfaller, WA Kaufmann, A Flörl, ...
Traffic 14 (8), 886-894, 2013
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
Combining high‐pressure freezing with pre‐embedding immunogold electron microscopy and tomography
MW Hess, GF Vogel, TE Yordanov, B Witting, K Gutleben, HL Ebner, ...
Traffic 19 (8), 639-649, 2018
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
Mü ller M, Lindner H, Hess MW, Teis D. 2014. Coordinated binding of Vps4 to ESCRT-III drives membrane neck constriction during MVB vesicle formation
MA Adell, GF Vogel, M Pakdel
The Journal of Cell Biology 205, 33-49, 0
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
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
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