Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis

Por Vester Udo, Grasemann Corinna, Schwiertz Raphael, Grasemann Hartmut, Racké Kurt, Ratjen Felix
Publicado em 2006-06-01

Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis

Por Grasemann, Hartmut, Schwiertz, Raphael, Grasemann, Corinna, Vester, Udo, Racké, Kurt, Ratjen, Felix
Publicado em 2006

Cyclosporine-A-induced nephrotoxicity in children with minimal-change nephrotic syndrome: long-term treatment up to 10 years

Por Kranz, Birgitta, Vester, Udo, Büscher, Rainer, Wingen, Anne-Margret, Hoyer, Peter F.
Publicado em 2008

Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome

Por Mache, Christoph J., Acham-Roschitz, Birgit, Frémeaux-Bacchi, Veronique, Kirschfink, Michael, Zipfel, Peter F., Roedl, Siegfried, Vester, Udo, Ring, Ekkehard
Publicado em 2009

Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathy

Por Bockmeyer, Clemens L., Säuberlich, Karen, Wittig, Juliane, Eßer, Marc, Roeder, Sebastian S., Vester, Udo, Hoyer, Peter F., Agustian, Putri A., Zeuschner, Philip, Amann, Kerstin, Daniel, Christoph, Becker, Jan U.
Publicado no Sci Rep (2016)

Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome

Por Hofer, Johannes, Janecke, Andreas R., Zimmerhackl, L.B., Riedl, Magdalena, Rosales, Alejandra, Giner, Thomas, Cortina, Gerard, Haindl, Carola J., Petzelberger, Barbara, Pawlik, Miriam, Jeller, Verena, Vester, Udo, Gadner, Bettina, van Husen, Michael, Moritz, Michael L., Würzner, Reinhard, Jungraithmayr, Therese
Publicado em 2013

Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo

Por Heinemann, Falko M., Jindra, Peter T., Bockmeyer, Clemens L., Zeuschner, Philip, Wittig, Juliane, Höflich, Heike, Eßer, Marc, Abbas, Mahmoud, Dieplinger, Georg, Stolle, Katharina, Vester, Udo, Hoyer, Peter F., Immenschuh, Stephan, Heinold, Andreas, Horn, Peter A., Li, Wentian, Eisenberger, Ute, Becker, Jan U.
Publicado no Sci Rep (2017)

Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo

Por Heinemann, Falko M., Jindra, Peter T., Bockmeyer, Clemens L., Zeuschner, Philip, Wittig, Juliane, Höflich, Heike, Eßer, Marc, Abbas, Mahmoud, Dieplinger, Georg, Stolle, Katharina, Vester, Udo, Hoyer, Peter F., Immenschuh, Stephan, Heinold, Andreas, Horn, Peter A., Li, Wentian, Eisenberger, Ute, Becker, Jan U.
Publicado no Sci Rep (2018)

Mutations in DZIP1L, which encodes a ciliary transition zone protein, cause autosomal recessive polycystic kidney disease

Por Lu, Hao, Galeano, Maria C. Rondón, Ott, Elisabeth, Kaeslin, Geraldine, Kausalya, P. Jaya, Kramer, Carina, Ortiz-Brüchle, Nadina, Hilger, Nadescha, Metzis, Vicki, Hiersche, Milan, Tay, Shang Yew, Tunningley, Robert, Vij, Shubha, Courtney, Andrew D., Whittle, Belinda, Wühl, Elke, Vester, Udo, Hartleben, Björn, Neuber, Steffen, Frank, Valeska, Little, Melissa H., Epting, Daniel, Papathanasiou, Peter, Perkins, Andrew C., Wright, Graham D., Hunziker, Walter, Gee, Heon Yung, Otto, Edgar A., Zerres, Klaus, Hildebrandt, Friedhelm, Roy, Sudipto, Wicking, Carol, Bergmann, Carsten
Publicado no Nat Genet (2017)

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

Mutations in the evolutionarily highly conserved KEOPS complex genes cause nephrotic syndrome with microcephaly

Por Braun, Daniela A., Rao, Jia, Mollet, Geraldine, Schapiro, David, Daugeron, Marie-Claire, Tan, Weizhen, Gribouval, Olivier, Boyer, Olivia, Revy, Patrick, Jobst-Schwan, Tilman, Schmidt, Johanna Magdalena, Lawson, Jennifer A., Schanze, Denny, Ashraf, Shazia, Boddaert, Nathalie, Collinet, Bruno, Martin, Gaëlle, Liger, Dominique, Lovric, Svjetlana, Furlano, Monica, Guerrera, I. Chiara, Sanchez-Ferras, Oraly, Menten, Björn, Vergult, Sarah, De Rocker, Nina, Airik, Merlin, Hermle, Tobias, Shril, Shirlee, Widmeier, Eugen, Gee, Heon Yung, Choi, Won-Il, Sadowski, Carolin E., Pabst, Werner L., Warejko, Jillian, Daga, Ankana, LeBerre, Tamara Basta, Matejas, Verena, Behnam, Babak, Beeson, Brendan, Begtrup, Amber, Bruce, Malcolm, Ch'ng, Gaik-Siew, Lin, Shuan-Pei, Chang, Jui-Hsing, Chen, Chao-Huei, Cho, Megan T., Gipson, Patrick E., Hsu, Chyong-Hsin, Kari, Jameela A., Ke, Yu-Yuan, Kiraly-Borri, Cathy, Lai, Wai-ming, Lemyre, Emmanuelle, Littlejohn, Rebecca Okasha, Masri, Amira, Moghtaderi, Mastaneh, Nakamura, Kazuyuki, Praet, Marleen, Prasad, Chitra, Prytula, Agnieszka, Roeder, Elizabeth, Rump, Patrick, Schnur, Rhonda E., Shiihara, Takashi, Sinha, Manish, Soliman, Neveen A, Soulami, Kenza, Sweetser, David A., Tsai, Wen-Hui, Tsai, Jeng-Daw, Vester, Udo, Viskochil, David H., Vatanavicharn, Nithiwat, Waxler, Jessica L., Wolf, Matthias T.F., Wong, Sik-Nin, Poduri, Annapurna, Truglio, Gessica, Mane, Shrikant, Lifton, Richard P., Bouchard, Maxime, Kannu, Peter, Chitayat, David, Magen, Daniella, Calleweart, Bert, van Tilbeurgh, Herman, Zenker, Martin, Antignac, Corinne, Hildebrandt, Friedhelm
Publicado no Nat Genet (2017)