![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach:
Dokumententyp
| Veröffentlichungsdatum
Springe zu: Zeitschriftenartikel
Anzahl der Publikationen: 6
Zeitschriftenartikel
Renner, Ellen D.; Kraetz, Carolin E.; Orange, Jordan S.; Hagl, Beate; Rylaarsdam, Stacey; Notheis, Gundula; Durandy, Anne; Torgerson, Troy R. und Ochs, Hans D.
(2021):
Class Switch Recombination Defects: impact on B cell maturation and antibody responses.
In: Clinical Immunology, Bd. 222, 108638
Makedonas, George; Mehta, Satish; Chouker, Alexander; Simpson, Richard J.; Marshall, Gailen; Orange, Jordan S.; Aunon-Chancellor, Serena; Smith, Scott M.; Zwart, Sara R.; Stowe, Raymond P.; Heer, Martina; Ponomarev, Sergey; Whitmire, Alexandra; Frippiat, Jean P.; Douglas, Grace L.; Krieger, Stephanie S.; Lorenzi, Hernan; Buchheim, Judith-Irina; Ginsburg, Geoffrey S.; Ott, C. Mark; Downs, Meghan; Pierson, Duane; Baecker, Natalie; Sams, Clarence und Crucian, Brian
(11. Oktober 2019):
Specific Immunologic Countermeasure Protocol for Deep-Space Exploration Missions.
In: Frontiers in Immunology, Bd. 10, 2407
[PDF, 216kB]
Somekh, Ido; Thian, Marini; Medgyesi, David; Gulez, Nesrin; Magg, Thomas; Gallon Duque, Alejandro; Stauber, Tali; Lev, Atar; Genel, Ferah; Unal, Ekrem; Simon, Amos J.; Lee, Yu Nee; Kalinichenko, Artem; Dmytrus, Jasmin; Kraakman, Michael J.; Schiby, Ginette; Rohlfs, Meino; Jacobson, Jeffrey M.; Ozer, Erdener; Akcal, Omer; Conca, Raffaele; Patiroglu, Turkan; Karakukcu, Musa; Ozcan, Alper; Shahin, Tala; Appella, Eliana; Tatematsu, Megumi; Martinez-Jaramillo, Catalina; Chinn, Ivan K.; Orange, Jordan S.; Milena Trujillo-Vargas, Claudia; Luis Franco, Jose; Hauck, Fabian; Somech, Raz; Klein, Christoph und Boztug, Kaan
(2019):
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis.
In: Blood, Bd. 134, Nr. 18: S. 1510-1516
Hagl, Beate; Spielberger, Benedikt D.; Thoene, Silvia; Bonnal, Sophie; Mertes, Christian; Winter, Christof; Nijman, Isaac J.; Verduin, Shira; Eberherr, Andreas C.; Puel, Anne; Schindler, Detlev; Ruland, Jürgen; Meitinger, Thomas; Gagneur, Julien; Orange, Jordan S.; Gijn, Marielle E. van und Renner, Ellen D.
(2018):
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation.
In: Scientific Reports, Bd. 8, 16719
[PDF, 3MB]
Netter, Petra; Chan, Sanny K.; Banerjee, Pinaki P.; Monaco-Shawver, Linda; Noroski, Lenora M.; Hanson, Imelda C.; Forbes, Lisa R.; Mace, Emily M.; Chinen, Javier; Gaspar, H. Bobby; Sleiman, Patrick; Hakonarson, Hakon; Klein, Christoph; Ehlayel, Mohammad S. und Orange, Jordan S.
(2016):
A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism.
In: Journal of Allergy and Clinical Immunology, Bd. 138, Nr. 2: S. 599-601
Li, Jin; Jørgensen, Silje F.; Maggadottir, S. Melkorka; Bakay, Marina; Warnatz, Klaus; Glessner, Joseph; Pandey, Rahul; Salzer, Ulrich; Schmidt, Reinhold E.; Perez, Elena; Resnick, Elena; Goldacker, Sigune; Buchta, Mary; Witte, Torsten; Padyukov, Leonid; Videm, Vibeke; Folseraas, Trine; Atschekzei, Faranaz; Elder, James T.; Nair, Rajan P.; Winkelmann, Juliane; Gieger, Christian; Nöthen, Markus M.; Büning, Carsten; Brand, Stephan; Sullivan, Kathleen E.; Orange, Jordan S.; Fevang, Børre; Schreiber, Stefan; Lieb, Wolfgang; Aukrust, Pål; Chapel, Helen; Cunningham-Rundles, Charlotte; Franke, Andre; Karlsen, Tom H.; Grimbacher, Bodo; Hakonarson, Hakon; Hammarström, Lennart und Ellinghaus, Eva
(2015):
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells.
In: Nature Communications, Bd. 6, 6804
[PDF, 807kB]