Bernhard Schermer
Bernhard Schermer
Nephrolab Cologne
Verified email at - Homepage
Cited by
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A mammalian microRNA expression atlas based on small RNA library sequencing
P Landgraf, M Rusu, R Sheridan, A Sewer, N Iovino, A Aravin, S Pfeffer, ...
Cell 129 (7), 1401-1414, 2007
Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways
M Simons, J Gloy, A Ganner, A Bullerkotte, M Bashkurov, C Krönig, ...
Nature genetics 37 (5), 537-543, 2005
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
EA Otto, B Schermer, T Obara, JF O'Toole, KS Hiller, AM Mueller, RG Ruf, ...
Nature genetics 34 (4), 413-420, 2003
Nephrin and CD2AP associate with phosphoinositide 3-OH kinase and stimulate AKT-dependent signaling
TB Huber, B Hartleben, J Kim, M Schmidts, B Schermer, A Keil, L Egger, ...
Molecular and cellular biology 23 (14), 4917-4928, 2003
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
H Olbrich, M Fliegauf, J Hoefele, A Kispert, E Otto, A Volz, MT Wolf, ...
Nature genetics 34 (4), 455-459, 2003
Podocyte-specific deletion of dicer alters cytoskeletal dynamics and causes glomerular disease
SJ Harvey, G Jarad, J Cunningham, S Goldberg, B Schermer, BD Harfe, ...
Journal of the American Society of Nephrology 19 (11), 2150-2158, 2008
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
M Chaki, R Airik, AK Ghosh, RH Giles, R Chen, GG Slaats, H Wang, ...
Cell 150 (3), 533-548, 2012
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
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels
TB Huber, B Schermer, RU Müller, M Höhne, M Bartram, A Calixto, ...
Proceedings of the National Academy of Sciences 103 (46), 17079-17086, 2006
Trafficking of TRPP2 by PACS proteins represents a novel mechanism of ion channel regulation
M Köttgen, T Benzing, T Simmen, R Tauber, B Buchholz, S Feliciangeli, ...
The EMBO journal 24 (4), 705-716, 2005
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome
I Ebermann, JB Phillips, MC Liebau, RK Koenekoop, B Schermer, I Lopez, ...
The Journal of clinical investigation 120 (6), 1812-1823, 2010
Repression of the genome organizer SATB1 in regulatory T cells is required for suppressive function and inhibition of effector differentiation
M Beyer, Y Thabet, RU Müller, T Sadlon, S Classen, K Lahl, S Basu, ...
Nature immunology 12 (9), 898-907, 2011
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics
C Dafinger, MC Liebau, SM Elsayed, Y Hellenbroich, E Boltshauser, ...
The Journal of clinical investigation 121 (7), 2662-2667, 2011
The von Hippel-Lindau tumor suppressor protein controls ciliogenesis by orienting microtubule growth
B Schermer, C Ghenoiu, M Bartram, RU Müller, F Kotsis, M Höhne, ...
The Journal of cell biology 175 (4), 547-554, 2006
The carboxyl terminus of Neph family members binds to the PDZ domain protein zonula occludens-1
TB Huber, M Schmidts, P Gerke, B Schermer, A Zahn, B Hartleben, ...
Journal of Biological Chemistry 278 (15), 13417-13421, 2003
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia
M Fliegauf, J Horvath, C von Schnakenburg, H Olbrich, D Müller, ...
Journal of the American Society of Nephrology 17 (9), 2424-2433, 2006
Tracking the fate of glomerular epithelial cells in vivo using serial multiphoton imaging in new mouse models with fluorescent lineage tags
MJ Hackl, JL Burford, K Villanueva, L Lam, K Suszták, B Schermer, ...
Nature medicine 19 (12), 1661-1666, 2013
NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway
S Habbig, MP Bartram, RU Müller, R Schwarz, N Andriopoulos, S Chen, ...
Journal of Cell Biology 193 (4), 633-642, 2011
14-3-3 interacts with regulator of G protein signaling proteins and modulates their activity
T Benzing, MB Yaffe, T Arnould, L Sellin, B Schermer, B Schilling, ...
Journal of Biological Chemistry 275 (36), 28167-28172, 2000
Dysregulated autophagy contributes to podocyte damage in Fabry’s disease
MC Liebau, F Braun, K Höpker, C Weitbrecht, V Bartels, RU Müller, ...
PloS one 8 (5), e63506, 2013
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