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Soeren Lienkamp
Soeren Lienkamp
Univerity of Zurich, Switzerland
Verified email at uzh.ch
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Cited by
Cited by
Year
3D U-Net: learning dense volumetric segmentation from sparse annotation
Ö Çiçek, A Abdulkadir, SS Lienkamp, T Brox, O Ronneberger
Medical Image Computing and Computer-Assisted Intervention–MICCAI 2016: 19th …, 2016
82272016
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia
C Bergmann, M Fliegauf, NO Brüchle, V Frank, H Olbrich, J Kirschner, ...
The American Journal of Human Genetics 82 (4), 959-970, 2008
3962008
Medical image computing and computer-assisted intervention–MICCAI 2016
Ö Çiçek, A Abdulkadir, SS Lienkamp, T Brox, O Ronneberger
19th International Conference, Athens, Greece, 424-432, 2016
379*2016
Vertebrate kidney tubules elongate using a planar cell polarity–dependent, rosette-based mechanism of convergent extension
SS Lienkamp, K Liu, CM Karner, TJ Carroll, O Ronneberger, ...
Nature genetics 44 (12), 1382-1387, 2012
2592012
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3
S Hoff, J Halbritter, D Epting, V Frank, TMT Nguyen, J Van Reeuwijk, ...
Nature genetics 45 (8), 951-956, 2013
2212013
Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors
MM Kaminski, J Tosic, C Kresbach, H Engel, J Klockenbusch, AL Müller, ...
Nature cell biology 18 (12), 1269-1280, 2016
1472016
Inversin, Wnt signaling and primary cilia
S Lienkamp, A Ganner, G Walz
Differentiation 83 (2), S49-S55, 2012
1132012
Genetic and physical interaction between the NPHP5 and NPHP6 gene products
T Schäfer, M Pütz, S Lienkamp, A Ganner, A Bergbreiter, ...
Human molecular genetics 17 (23), 3655-3662, 2008
1052008
Cyclin O (Ccno) functions during deuterosome‐mediated centriole amplification of multiciliated cells
MC Funk, AN Bera, T Menchen, G Kuales, K Thriene, SS Lienkamp, ...
The EMBO journal 34 (8), 1078-1089, 2015
952015
Mutations in TBX18 cause dominant urinary tract malformations via transcriptional dysregulation of ureter development
A Vivante, MJ Kleppa, J Schulz, S Kohl, A Sharma, J Chen, S Shril, ...
The American Journal of Human Genetics 97 (2), 291-301, 2015
932015
The C/EBP homologous protein CHOP (GADD153) is an inhibitor of Wnt/TCF signals
M Horndasch, S Lienkamp, E Springer, A Schmitt, H Pavenstädt, G Walz, ...
Oncogene 25 (24), 3397-3407, 2006
712006
Inversin relays Frizzled-8 signals to promote proximal pronephros development
S Lienkamp, A Ganner, C Boehlke, T Schmidt, SJ Arnold, T Schäfer, ...
Proceedings of the National Academy of Sciences 107 (47), 20388-20393, 2010
682010
The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin
D Epting, K Slanchev, C Boehlke, S Hoff, NT Loges, T Yasunaga, L Indorf, ...
Development 142 (1), 174-184, 2015
622015
Regulation of ciliary polarity by the APC/C
A Ganner, S Lienkamp, T Schäfer, D Romaker, T Wegierski, TJ Park, ...
Proceedings of the National Academy of Sciences 106 (42), 17799-17804, 2009
612009
The polarity protein Inturned links NPHP4 to Daam1 to control the subapical actin network in multiciliated cells
T Yasunaga, S Hoff, C Schell, M Helmstädter, O Kretz, S Kuechlin, ...
Journal of Cell Biology 211 (5), 963-973, 2015
572015
A dominant mutation in nuclear receptor interacting protein 1 causes urinary tract malformations via dysregulation of retinoic acid signaling
A Vivante, N Mann, H Yonath, AC Weiss, M Getwan, MM Kaminski, ...
Journal of the American Society of Nephrology 28 (8), 2364-2376, 2017
532017
Anks3 interacts with nephronophthisis proteins and is required for normal renal development
TA Yakulov, T Yasunaga, H Ramachandran, C Engel, B Müller, S Hoff, ...
Kidney international 87 (6), 1191-1200, 2015
422015
Molecular basis for autosomal-dominant renal Fanconi syndrome caused by HNF4A
V Marchesin, A Pérez-Martí, G Le Meur, R Pichler, K Grand, ED Klootwijk, ...
Cell reports 29 (13), 4407-4421. e5, 2019
412019
Using Xenopus to study genetic kidney diseases
SS Lienkamp
Seminars in cell & developmental biology 51, 117-124, 2016
402016
Network for early Onset cystic Kidney Diseases—A comprehensive Multidisciplinary Approach to Hereditary cystic Kidney Diseases in childhood
JC König, A Titieni, M Konrad, Neocyst Consortium
Frontiers in Pediatrics 6, 24, 2018
322018
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