The Centrosomal Kinase Plk1 Localizes to the Transition Zone of Primary Cilia and Induces Phosphorylation of Nephrocystin-1

Por Seeger-Nukpezah, Tamina, Liebau, Max C., Höpker, Katja, Lamkemeyer, Tobias, Benzing, Thomas, Golemis, Erica A., Schermer, Bernhard
Publicado em 2012

The Ciliary Protein Nephrocystin-4 Translocates the Canonical Wnt Regulator Jade-1 to the Nucleus to Negatively Regulate β-Catenin Signaling

Por Borgal, Lori, Habbig, Sandra, Hatzold, Julia, Liebau, Max C., Dafinger, Claudia, Sacarea, Ilinca, Hammerschmidt, Matthias, Benzing, Thomas, Schermer, Bernhard
Publicado em 2012

Dysregulated Autophagy Contributes to Podocyte Damage in Fabry’s Disease

Por Liebau, Max C., Braun, Fabian, Höpker, Katja, Weitbrecht, Claudia, Bartels, Valerie, Müller, Roman-Ulrich, Brodesser, Susanne, Saleem, Moin A., Benzing, Thomas, Schermer, Bernhard, Cybulla, Markus, Kurschat, Christine E.
Publicado em 2013

NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway

Por Habbig, Sandra, Bartram, Malte P., Müller, Roman U., Schwarz, Ricarda, Andriopoulos, Nikolaos, Chen, Shuhua, Sägmüller, Josef G., Hoehne, Martin, Burst, Volker, Liebau, Max C., Reinhardt, H. Christian, Benzing, Thomas, Schermer, Bernhard
Publicado em 2011

Protection of Human Podocytes from Shiga Toxin 2-Induced Phosphorylation of Mitogen-Activated Protein Kinases and Apoptosis by Human Serum Amyloid P Component

Por Dettmar, Anne K., Binder, Elisabeth, Greiner, Friederike R., Liebau, Max C., Kurschat, Christine E., Jungraithmayr, Therese C., Saleem, Moin A., Schmitt, Claus-Peter, Feifel, Elisabeth, Orth-Höller, Dorothea, Kemper, Markus J., Pepys, Mark, Würzner, Reinhard, Oh, Jun
Publicado em 2014

Nephrocystin-4 Regulates Pyk2-induced Tyrosine Phosphorylation of Nephrocystin-1 to Control Targeting to Monocilia

Por Liebau, Max C., Höpker, Katja, Müller, Roman U., Schmedding, Ingolf, Zank, Sibylle, Schairer, Benjamin, Fabretti, Francesca, Höhne, Martin, Bartram, Malte P., Dafinger, Claudia, Hackl, Matthias, Burst, Volker, Habbig, Sandra, Zentgraf, Hanswalter, Blaukat, Andree, Walz, Gerd, Benzing, Thomas, Schermer, Bernhard
Publicado em 2011

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

Por Ebermann, Inga, Phillips, Jennifer B., Liebau, Max C., Koenekoop, Robert K., Schermer, Bernhard, Lopez, Irma, Schäfer, Ellen, Roux, Anne-Francoise, Dafinger, Claudia, Bernd, Antje, Zrenner, Eberhart, Claustres, Mireille, Blanco, Bernardo, Nürnberg, Gudrun, Nürnberg, Peter, Ruland, Rebecca, Westerfield, Monte, Benzing, Thomas, Bolz, Hanno J.
Publicado em 2010

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

Por Ebermann, Inga, Phillips, Jennifer B., Liebau, Max C., Koenekoop, Robert K., Schermer, Bernhard, Lopez, Irma, Schäfer, Ellen, Roux, Anne-Francoise, Dafinger, Claudia, Bernd, Antje, Zrenner, Eberhart, Claustres, Mireille, Blanco, Bernardo, Nürnberg, Gudrun, Nürnberg, Peter, Ruland, Rebecca, Westerfield, Monte, Benzing, Thomas, Bolz, Hanno J.
Publicado em 2011

AATF/Che-1 acts as a phosphorylation-dependent molecular modulator to repress p53-driven apoptosis

Por Höpker, Katja, Hagmann, Henning, Khurshid, Safiya, Chen, Shuhua, Hasskamp, Pia, Seeger-Nukpezah, Tamina, Schilberg, Katharina, Heukamp, Lukas, Lamkemeyer, Tobias, Sos, Martin L, Thomas, Roman K, Lowery, Drew, Roels, Frederik, Fischer, Matthias, Liebau, Max C, Resch, Ulrike, Kisner, Tülay, Röther, Fabian, Bartram, Malte P, Müller, Roman Ulrich, Fabretti, Francesca, Kurschat, Peter, Schumacher, Björn, Gaestel, Matthias, Medema, René H, Yaffe, Michael B, Schermer, Bernhard, Reinhardt, H Christian, Benzing, Thomas
Publicado em 2012

CONSENSUS EXPERT RECOMMENDATIONS FOR THE DIAGNOSIS AND MANAGEMENT OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE: REPORT OF AN INTERNATIONAL CONFERENCE

Por Guay-Woodford, Lisa M., Bissler, John J., Braun, Michael C., Bockenhauer, Detlef, Cadnapaphornchai, Melissa A., Dell, Katherine M., Kerecuk, Larissa, Liebau, Max C., Alonso-Peclet, Maria H., Shneider, Benjamin, Emre, Sukru, Heller, Theo, Kamath, Binita M., Murray, Karen F., Moise, Kenneth, Eichenwald, Eric E., Evans, Jacquelyn, Keller, Roberta L., Wilkins-Haug, Louise, Bergmann, Carsten, Gunay-Aygun, Meral, Hooper, Stephen R., Hardy, Kristina K., Hartung, Erum A., Streisand, Randi, Perrone, Ronald, Moxey-Mims, Marva
Publicado no J Pediatr (2014)

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

Por Chaki, Moumita, Airik, Rannar, Ghosh, Amiya K., Giles, Rachel H., Chen, Rui, Slaats, Gisela G., Wang, Hui, Hurd, Toby W., Zhou, Weibin, Cluckey, Andrew, Gee, Heon-Yung, Ramaswami, Gokul, Hong, Chen-Jei, Hamilton, Bruce A., Červenka, Igor, Ganji, Ranjani Sri, Bryja, Vitezslav, Arts, Heleen H., van Reeuwijk, Jeroen, Oud, Machteld M., Letteboer, Stef J.F., Roepman, Ronald, Husson, Hervé, Ibraghimov-Beskrovnaya, Oxana, Ysunaga, Takayuki, Walz, Gerd, Eley, Lorraine, Sayer, John A., Schermer, Bernhard, Liebau, Max C., Benzing, Thomas, Le Corre, Stephanie, Drummond, Iain, Joles, Jaap A., Janssen, Sabine, Allen, Susan J., Natarajan, Sivakumar, O Toole, John F., Attanasio, Massimo, Saunier, Sophie, Antignac, Corinne, Koenekoop, Robert K., Ren, Huanan, Lopez, Irma, Nayir, Ahmet, Stoetzel, Corinne, Dollfus, Helene, Massoudi, Rustin, Gleeson, Joseph G., Andreoli, Sharon P., Doherty, Dan G., Lindstrad, Anna, Golzio, Christelle, Katsanis, Nicholas, Pape, Lars, Abboud, Emad B., Al-Rajhi, Ali A., Lewis, Richard A., Lupski, James R., Omran, Heymut, Lee, Eva, Wang, Shaohui, Sekiguchi, JoAnn M., Saunders, Rudel, Johnson, Colin A., Garner, Elizabeth, Vanselow, Katja, Andersen, Jens S., Shlomai, Joseph, Nurnberg, Gudrun, Nurnberg, Peter, Levy, Shawn, Smogorzewska, Agata, Otto, Edgar A., Hildebrandt, Friedhelm
Publicado em 2012