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2021
Maccari, Maria Elena, Fuchs, Sebastian, Kury, Patrick, Andrieux, Geoffroy, Volkl, Simon ORCID: 0000-0003-2193-3048, Bengsch, Bertram ORCID: 0000-0003-2552-740X, Lorenz, Myriam Ricarda, Heeg, Maximilian, Rohr, Jan, Jagle, Sabine, Castro, Carla N., Gross, Miriam, Warthorst, Ursula, Koenig, Christoph, Fuchs, Ilka, Speckmann, Carsten, Thalhammer, Julian ORCID: 0000-0002-0226-1955, Kapp, Friedrich G., Seidel, Markus G., Duckers, Gregor, Schoenberger, Stefan, Schuetz, Catharina, Fuhrer, Marita, Kobbe, Robin, Holzinger, Dirk, Klemann, Christian ORCID: 0000-0002-5639-8690, Smisek, Petr, Owens, Stephen, Horneff, Gerd, Kolb, Reinhard, Naumann-Bartsch, Nora, Miano, Maurizio ORCID: 0000-0002-9816-1704, Staniek, Julian, Rizzi, Marta ORCID: 0000-0002-5153-6089, Kalina, Tomas ORCID: 0000-0003-4475-2872, Schneider, Pascal, Erxleben, Anika, Backofen, Rolf, Ekici, Arif, Niemeyer, Charlotte M., Warnatz, Klaus, Grimbacher, Bodo, Eibel, Hermann, Mackensen, Andreas, Frei, Andreas Philipp, Schwarz, Klaus, Boerries, Melanie, Ehl, Stephan ORCID: 0000-0002-9265-2721 and Rensing-Ehl, Anne (2021). A distinct CD38(+)CD45RA(+) population of CD4(+), CD8(+), and double-negative T cells is controlled by FAS. J. Exp. Med., 218 (2). NEW YORK: ROCKEFELLER UNIV PRESS. ISSN 1540-9538
2020
Ammann, Sandra, Fuchs, Sebastian, Martin-Martin, Lydia, Castro, Carla N., Spielberger, Benedikt ORCID: 0000-0002-0300-0730, Klemann, Christian, Elling, Roland, Heeg, Maximilian, Speckmann, Carsten, Hainmann, Ina, Kaiser-Labusch, Petra, Horneff, Gerd, Thalhammer, Julian, Bredius, Robbert G., zur Stadt, Udo, Lehmberg, Kai, Fuchs, Ilka, von Spee-Mayer, Caroline ORCID: 0000-0002-0560-7915, Henneke, Philipp and Ehl, Stephan (2020). Functional flow cytometry of monocytes for routine diagnosis of innate primary immunodeficiencies. J. Allergy Clin. Immunol., 145 (1). S. 434 - 438. NEW YORK: MOSBY-ELSEVIER. ISSN 1097-6825
2016
Ammann, Sandra ORCID: 0000-0003-0385-1890, Schulz, Ansgar, Kraegeloh-Mann, Ingeborg, Dieckmann, Nele M. G., Niethammer, Klaus, Fuchs, Sebastian ORCID: 0000-0001-9191-7970, Eckl, Katja Martina, Plank, Roswitha, Werner, Roland, Altmueller, Janine, Thiele, Holger, Nuernberg, Peter, Bank, Julia, Strauss, Anne, von Bernuth, Horst, zur Stadt, Udo, Grieve, Samantha, Griffiths, Gillian M., Lehmberg, Kai, Hennies, Hans Christian and Ehl, Stephan (2016). Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). S. 997 - 1007. WASHINGTON: AMER SOC HEMATOLOGY. ISSN 1528-0020