Items where Author is "Hildebrandt, Friedhelm"

2021

Vavassori, Stefano and Chou, Janet and Faletti, Laura Eva and Haunerdinger, Veronika and Opitz, Lennart and Joset, Pascal and Fraser, Christopher J. and Prader, Seraina and Gao, Xianfei and Schuch, Luise A. and Wagner, Matias and Hoefele, Julia and Maccari, Maria Elena and Zhu, Ying and Elakis, George and Gabbett, Michael T. and Forstner, Maria and Omran, Heymut and Kaiser, Thomas and Kessler, Christina and Olbrich, Heike and Frosk, Patrick and Almutairi, Abduarahman and Platt, Craig D. and Elkins, Megan and Weeks, Sabrina and Rubin, Tamar and Planas, Raquel and Marchetti, Tommaso and Koovely, Danil and Klämbt, Verena and Soliman, Neveen A. and von Hardenberg, Sandra and Klemann, Christian and Baumann, Ulrich and Lenz, Dominic and Klein-Franke, Andreas and Schwemmle, Martin and Huber, Michael and Sturm, Ekkehard and Hartleif, Steffen and Häffner, Karsten and Gimpel, Charlotte and Brotschi, Barbara and Laube, Guido and Güngör, Tayfun and Buckley, Michael F. and Kottke, Raimund and Staufner, Christian and Hildebrandt, Friedhelm and Reu-Hofer, Simone and Moll, Solange and Weber, Achim and Kaur, Hundeep and Ehl, Stephan and Hiller, Sebastian and Geha, Raif and Roscioli, Tony and Griese, Matthias and Pachlopnik Schmid, Jana. (2021) Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency. The Journal of Allergy & Clinical Immunology, 148 (2). pp. 381-393.

2006

Sayer, John A. and Otto, Edgar A. and O'Toole, John F. and Nurnberg, Gudrun and Kennedy, Michael A. and Becker, Christian and Hennies, Hans Christian and Helou, Juliana and Attanasio, Massimo and Fausett, Blake V. and Utsch, Boris and Khanna, Hemant and Liu, Yan and Drummond, Iain and Kawakami, Isao and Kusakabe, Takehiro and Tsuda, Motoyuki and Ma, Li and Lee, Hwankyu and Larson, Ronald G. and Allen, Susan J. and Wilkinson, Christopher J. and Nigg, Erich A. and Shou, Chengchao and Lillo, Concepcion and Williams, David S. and Hoppe, Bernd and Kemper, Markus J. and Neuhaus, Thomas and Parisi, Melissa A. and Glass, Ian A. and Petry, Marianne and Kispert, Andreas and Gloy, Joachim and Ganner, Athina and Walz, Gerd and Zhu, Xueliang and Goldman, Daniel and Nurnberg, Peter and Swaroop, Anand and Leroux, Michel R. and Hildebrandt, Friedhelm. (2006) The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nature genetics, Vol. 38, H. 6. pp. 674-681.