Tbx18 regulates the development of the ureteral mesenchyme

Por Airik, Rannar, Bussen, Markus, Singh, Manvendra K., Petry, Marianne, Kispert, Andreas
Publicado em 2006

The prepattern transcription factor Irx3 directs nephron segment identity

Por Reggiani, Luca, Raciti, Daniela, Airik, Rannar, Kispert, Andreas, Brändli, André W.
Publicado em 2007

SDCCAG8 Regulates Pericentriolar Material Recruitment and Neuronal Migration in the Developing Cortex

Por Insolera, Ryan, Shao, Wei, Airik, Rannar, Hildebrandt, Friedhelm, Shi, Song-Hai
Publicado em 2014

Roscovitine blocks collecting duct cyst growth in Cep164-deficient kidneys

Por Airik, Rannar, Airik, Merlin, Schueler, Markus, Bates, Carlton M., Hildebrandt, Friedhelm
Publicado no Kidney Int (2019)

TSHZ3 and SOX9 Regulate the Timing of Smooth Muscle Cell Differentiation in the Ureter by Reducing Myocardin Activity

Por Martin, Elise, Caubit, Xavier, Airik, Rannar, Vola, Christine, Fatmi, Ahmed, Kispert, Andreas, Fasano, Laurent
Publicado em 2013

Osteoclast stimulation factor 1 (Ostf1) KNOCKOUT increases trabecular bone mass in mice

Por Vermeren, Matthieu, Lyraki, Rodanthi, Wani, Sachin, Airik, Rannar, Albagha, Omar, Mort, Richard, Hildebrandt, Friedhelm, Hurd, Toby
Publicado no Mamm Genome (2017)

A FANCD2/FANCI-Associated Nuclease 1-Knockout Model Develops Karyomegalic Interstitial Nephritis

Por Airik, Rannar, Schueler, Markus, Airik, Merlin, Cho, Jang, Porath, Jonathan D., Mukherjee, Elina, Sims-Lucas, Sunder, Hildebrandt, Friedhelm
Publicado no J Am Soc Nephrol (2016)

Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q(10) deficiency()

Por Doimo, Mara, Trevisson, Eva, Airik, Rannar, Bergdoll, Marc, Santos-Ocaña, Carlos, Hildebrandt, Friedhelm, Navas, Placido, Pierrel, Fabien, Salviati, Leonardo
Publicado em 2014

Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium

Por Rudat, Carsten, Grieskamp, Thomas, Röhr, Christian, Airik, Rannar, Wrede, Christoph, Hegermann, Jan, Herrmann, Bernhard G., Schuster-Gossler, Karin, Kispert, Andreas
Publicado no PLoS One (2014)

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

Por Saisawat, Pawaree, Tasic, Velibor, Vega-Warner, Virginia, Kehinde, Elijah O., Günther, Barbara, Airik, Rannar, Innis, Jeffrey W., Hoskins, Bethan E., Hoefele, Julia, Otto, Edgar A., Hildebrandt, Friedhelm
Publicado em 2011

SDCCAG8 Interacts with RAB Effector Proteins RABEP2 and ERC1 and Is Required for Hedgehog Signaling

Por Airik, Rannar, Schueler, Markus, Airik, Merlin, Cho, Jang, Ulanowicz, Kelsey A., Porath, Jonathan D., Hurd, Toby W., Bekker-Jensen, Simon, Schrøder, Jacob M., Andersen, Jens S., Hildebrandt, Friedhelm
Publicado no PLoS One (2016)

Mutation analysis in Bardet–Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals

Por Janssen, Sabine, Ramaswami, Gokul, Davis, Erica E., Hurd, Toby, Airik, Rannar, Kasanuki, Jennifer M., Van Der Kraak, Lauren, Allen, Susan J., Beales, Philip L., Katsanis, Nicholas, Otto, Edgar A., Hildebrandt, Friedhelm
Publicado em 2010

Repression of Sox9 by Jag1 is continuously required to suppress the default chondrogenic fate of vascular smooth muscle cell

Por Briot, Anaïs, Jaroszewicz, Artur, Warren, Carmen M., Lu, Jing, Touma, Marlin, Rudat, Carsten, Hofmann, Jennifer J., Airik, Rannar, Weinmaster, Gerry, Lyons, Karen, Wang, Yibin, Kispert, Andreas, Pellegrini, Matteo, Iruela-Arispe, M. Luisa
Publicado no Dev Cell (2014)

Treatment with 2,4-Dihydroxybenzoic Acid Prevents FSGS Progression and Renal Fibrosis in Podocyte-Specific Coq6 Knockout Mice

Por Widmeier, Eugen, Airik, Merlin, Hugo, Hannah, Schapiro, David, Wedel, Johannes, Ghosh, Chandra C., Nakayama, Makiko, Schneider, Ronen, Awad, Agape M., Nag, Anish, Cho, Jang, Schueler, Markus, Clarke, Catherine F., Airik, Rannar, Hildebrandt, Friedhelm
Publicado no J Am Soc Nephrol (2019)

Renal-Retinal Ciliopathy Gene Sdccag8 Regulates DNA Damage Response Signaling

Por Airik, Rannar, Slaats, Gisela G., Guo, Zhi, Weiss, Anna-Carina, Khan, Naheed, Ghosh, Amiya, Hurd, Toby W., Bekker-Jensen, Simon, Schrøder, Jacob M., Elledge, Steve J., Andersen, Jens S., Kispert, Andreas, Castelli, Maddalena, Boletta, Alessandra, Giles, Rachel H., Hildebrandt, Friedhelm
Publicado em 2014

Mutation Analysis of 18 Nephronophthisis-associated Ciliopathy Disease Genes using a DNA Pooling and Next-Generation Sequencing Strategy

Por Otto, Edgar A., Ramaswami, Gokul, Janssen, Sabine, Chaki, Moumita, Allen, Susan J., Zhou, Weibin, Airik, Rannar, Hurd, Toby W., Ghosh, Amiya K., Wolf, Matthias T., Hoppe, Bernd, Neuhaus, Thomas J., Bockenhauer, Detlef, Milford, David V., Soliman, Neveen A., Saunier, Sophie, Johnson, Colin A., Hildebrandt, Friedhelm
Publicado em 2010

Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity

Por Braun, Daniela A., Schueler, Markus, Halbritter, Jan, Gee, Heon Yung, Porath, Jonathan D., Lawson, Jennifer A., Airik, Rannar, Shril, Shirlee, Allen, Susan J., Stein, Deborah, Al Kindy, Adila, Beck, Bodo B., Cengiz, Nurcan, Moorani, Khemchand N., Ozaltin, Fatih, Hashmi, Seema, Sayer, John A., Bockenhauer, Detlef, Soliman, Neveen A., Otto, Edgar A., Lifton, Richard P., Hildebrandt, Friedhelm
Publicado no Kidney Int (2016)

DCDC2 Mutations Cause a Renal-Hepatic Ciliopathy by Disrupting Wnt Signaling

Por Schueler, Markus, Braun, Daniela A., Chandrasekar, Gayathri, Gee, Heon Yung, Klasson, Timothy D., Halbritter, Jan, Bieder, Andrea, Porath, Jonathan D., Airik, Rannar, Zhou, Weibin, LoTurco, Joseph J., Che, Alicia, Otto, Edgar A., Böckenhauer, Detlef, Sebire, Neil J., Honzik, Tomas, Harris, Peter C., Koon, Sarah J., Gunay-Aygun, Meral, Saunier, Sophie, Zerres, Klaus, Bruechle, Nadina Ortiz, Drenth, Joost P.H., Pelletier, Laurence, Tapia-Páez, Isabel, Lifton, Richard P., Giles, Rachel H., Kere, Juha, Hildebrandt, Friedhelm
Publicado no Am J Hum Genet (2015)

FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair

Por Zhou, Weibin, Otto, Edgar A., Cluckey, Andrew, Airik, Rannar, Hurd, Toby W., Chaki, Moumita, Diaz, Katrina, Lach, Francis P., Bennett, Geoffrey R., Gee, Heon Y., Ghosh, Amiya K., Natarajan, Sivakumar, Thongthip, Supawat, Veturi, Uma, Allen, Susan J., Janssen, Sabine, Ramaswami, Gokul, Dixon, Joanne, Burkhalter, Felix, Spoendlin, Martin, Moch, Holger, Mihatsch, Michael J., Verine, Jerome, Reade, Richard, Soliman, Hany, Godin, Michel, Kiss, Denes, Monga, Guido, Mazzucco, Gianna, Amann, Kerstin, Artunc, Ferruh, Newland, Ronald C., Wiech, Thorsten, Zschiedrich, Stefan, Huber, Tobias B., Friedl, Andreas, Slaats, Gisela G., Joles, Jaap A., Goldschmeding, Roel, Washburn, Joseph, Giles, Rachel H., Levy, Shawn, Smogorzewska, Agata, Hildebrandt, Friedhelm
Publicado em 2012

Whole exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

Por Gee, Heon Yung, Otto, Edgar A., Hurd, Toby W., Ashraf, Shazia, Chaki, Moumita, Cluckey, Andrew, Vega-Warner, Virginia, Saisawat, Pawaree, Diaz, Katrina A., Fang, Humphrey, Kohl, Stefan, Allen, Susan J., Airik, Rannar, Zhou, Weibin, Ramaswami, Gokul, Janssen, Sabine, Fu, Clementine, Innis, Jamie L., Weber, Stefanie, Vester, Udo, Davis, Erica E., Katsanis, Nicholas, Fathy, Hanan M., Jeck, Nikola, Klaus, Gunther, Nayir, Ahmet, Rahim, Khawla A., Attrach, Ibrahim Al, Hassoun, Ibrahim Al, Ozturk, Savas, Drozdz, Dorota, Helmchen, Udo, O’Toole, John F., Attanasio, Massimo, Nürnberg, Gudrun, Nürnberg, Peter, Washburn, Joseph, MacDonald, James, James, Jeffrey W., Levy, Shawn, Hildebrandt, Friedhelm
Publicado em 2013