| SNARE protein structure and function D Ungar, FM Hughson Annual review of cell and developmental biology 19 (1), 493-517, 2003 | 445 | 2003 |
| Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function D Ungar, T Oka, EE Brittle, E Vasile, VV Lupashin, JE Chatterton, ... The Journal of cell biology 157 (3), 405-415, 2002 | 365 | 2002 |
| Retrograde transport on the COG railway D Ungar, T Oka, M Krieger, FM Hughson Trends in cell biology 16 (2), 113-120, 2006 | 163 | 2006 |
| The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins T Oka, D Ungar, FM Hughson, M Krieger Molecular biology of the cell 15 (5), 2423-2435, 2004 | 163 | 2004 |
| A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1–Cog8 interaction in COG complex formation F Foulquier, D Ungar, E Reynders, R Zeevaert, P Mills, MT García-Silva, ... Human molecular genetics 16 (7), 717-730, 2007 | 146 | 2007 |
| COG8 deficiency causes new congenital disorder of glycosylation type IIh C Kranz, BG Ng, L Sun, V Sharma, EA Eklund, Y Miura, D Ungar, ... Human molecular genetics 16 (7), 731-741, 2007 | 141 | 2007 |
| Subunit architecture of the conserved oligomeric Golgi complex D Ungar, T Oka, E Vasile, M Krieger, FM Hughson Journal of Biological Chemistry 280 (38), 32729-32735, 2005 | 140 | 2005 |
| The Golgi puppet master: COG complex at center stage of membrane trafficking interactions R Willett, D Ungar, V Lupashin Histochemistry and cell biology 140 (3), 271-283, 2013 | 128 | 2013 |
| Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation J Lübbehusen, C Thiel, N Rind, D Ungar, BH Prinsen, TJ de Koning, ... Human molecular genetics 19 (18), 3623-3633, 2010 | 114 | 2010 |
| COG complexes form spatial landmarks for distinct SNARE complexes R Willett, T Kudlyk, I Pokrovskaya, R Schönherr, D Ungar, R Duden, ... Nature communications 4 (1), 1553, 2013 | 109 | 2013 |
| Golgi linked protein glycosylation and associated diseases D Ungar Seminars in cell & developmental biology 20 (7), 762-769, 2009 | 104 | 2009 |
| Epithelial-to-mesenchymal transition drives a pro-metastatic Golgi compaction process through scaffolding protein PAQR11 X Tan, P Banerjee, HF Guo, S Ireland, D Pankova, Y Ahn, IM Nikolaidis, ... The Journal of clinical investigation 127 (1), 117-131, 2017 | 99 | 2017 |
| Genetic analysis of the subunit organization and function of the conserved oligomeric Golgi (COG) complex T Oka, E Vasile, M Penman, CD Novina, DM Dykxhoorn, D Ungar, ... Journal of Biological Chemistry 280 (38), 32736-32745, 2005 | 99 | 2005 |
| Re'COG'nition at the Golgi VJ Miller, D Ungar Traffic 13 (7), 891-897, 2012 | 95 | 2012 |
| Molecular insights into vesicle tethering at the Golgi by the conserved oligomeric Golgi (COG) complex and the golgin TATA element modulatory factor (TMF) VJ Miller, P Sharma, TA Kudlyk, L Frost, AP Rofe, IJ Watson, R Duden, ... Journal of Biological Chemistry 288 (6), 4229-4240, 2013 | 85 | 2013 |
| Filter-Aided N-Glycan Separation (FANGS): A Convenient Sample Preparation Method for Mass Spectrometric N-Glycan Profiling S Abdul Rahman, E Bergström, CJ Watson, KM Wilson, DA Ashford, ... Journal of proteome research 13 (3), 1167-1176, 2014 | 79 | 2014 |
| Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene BC Richardson, RD Smith, D Ungar, A Nakamura, PD Jeffrey, ... Proceedings of the National Academy of Sciences 106 (32), 13329-13334, 2009 | 78 | 2009 |
| COG Complex complexities: Detailed characterization of a complete set of HEK293T cells lacking individual COG subunits JB Blackburn, I Pokrovskaya, P Fisher, D Ungar, VV Lupashin Frontiers in cell and developmental biology 4, 23, 2016 | 69 | 2016 |
| Bridging the gap between glycosylation and vesicle traffic P Fisher, D Ungar Frontiers in cell and developmental biology 4, 15, 2016 | 66 | 2016 |
| Molecular and clinical characterization of a Moroccan Cog7 deficient patient BG Ng, C Kranz, EEO Hagebeuk, M Duran, N Abeling, B Wuyts, D Ungar, ... Molecular genetics and metabolism 91 (2), 201-204, 2007 | 63 | 2007 |
Vladimir LupashinProfessor of Physiology and Cell Biology, UAMSVerified email at uams.edu