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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 16

Zeitschriftenartikel

Raedler, Johannes; Magg, Thomas; Rohlfs, Meino; Klein, Christoph; Vallée, Tanja; Hauck, Fabian und Albert, Michael H. (2021): Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency. In: Journal of clinical immunology, Bd. 41, Nr. 7: S. 1536-1548 [PDF, 2MB]

Magg, Thomas; Okano, Tsubasa; Koenig, Lars M.; Boehmer, Daniel F. R.; Schwartz, Samantha L.; Inoue, Kento; Heimall, Jennifer; Licciardi, Francesco; Ley-Zaporozhan, Julia; Ferdman, Ronald M.; Caballero-Oteyza, Andres; Park, Esther N.; Calderon, Brenda M.; Dey, Debayan; Kanegane, Hirokazu; Cho, Kazutoshi; Montin, Davide; Reiter, Karl; Griese, Matthias; Albert, Michael H.; Rohlfs, Meino; Gray, Paul; Walz, Christoph; Conn, Graeme L.; Sullivan, Kathleen E.; Klein, Christoph; Morio, Tomohiro und Hauck, Fabian (2021): Heterozygous OAS1 gain-of-function variants cause an autoinflammatory immunodeficiency. In: Science Immunology, Bd. 6, Nr. 60, eabf9564

Raedler, Johannes; Magg, Thomas; Rohlfs, Meino; Klein, Christoph; Vallée, Tanja; Hauck, Fabian und Albert, Michael H. (2021): Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency. In: Journal of Clinical Immunology, Bd. 41, Nr. 7: S. 1536-1548

Bitar, Michael; Boettcher, Marcus; Boldt, Andreas; Hauck, Fabian; Koehl, Ulrike; Liebert, Uwe G.; Magg, Thomas; Schulz, Marian S. und Sack, Ulrich (2020): Flow cytometric measurement of STAT5 phosphorylation in cytomegalovirus-stimulated T cells. In: Cytometry Part A, Bd. 99, Nr. 8: S. 774-783

Heller, Stephanie; Koelsch, Uwe; Magg, Thomas; Krueger, Renate; Scheuern, Andrea; Schneider, Holm; Eichinger, Anna; Wahn, Volker; Unterwalder, Nadine; Lorenz, Myriam; Schwarz, Klaus; Meisel, Christian; Schulz, Ansgar; Hauck, Fabian und Bernuth, Horst von (2020): T Cell Impairment Is Predictive for a Severe Clinical Course in NEMO Deficiency. In: Journal of Clinical Immunology, Bd. 40, Nr. 3: S. 421-434

Boehmer, Daniel F. R.; Koehler, Lisa M.; Magg, Thomas; Metzger, Philipp; Rohlfs, Meino; Ahlfeld, Julia; Rack-Hoch, Anita; Reiter, Karl; Albert, Michael H.; Endres, Stefan; Rothenfusser, Simon; Klein, Christoph; König, Lars M. und Hauck, Fabian (2020): A Novel Complete Autosomal-Recessive STAT1 LOF Variant Causes Immunodeficiency with Hemophagocytic Lymphohistiocytosis-Like Hyperinflammation. In: Journal of Allergy and Clinical Immunology-in Practice, Bd. 8, Nr. 9: S. 3102-3111

Magg, Thomas; Shcherbina, Anna; Arslan, Duran; Desai, Mukesh M.; Wall, Sarah; Mitsialis, Vanessa; Conca, Raffaele; Unal, Ekrem; Karacabey, Neslihan; Mukhina, Anna; Rodina, Yulia; Taur, Prasad D.; Illig, David; Marquardt, Benjamin; Hollizeck, Sebastian; Jeske, Tim; Gothe, Florian; Schober, Tilmann; Rohlfs, Meino; Koletzko, Sibylle; Lurz, Eberhard; Muise, Aleixo M.; Snapper, Scott B.; Hauck, Fabian; Klein, Christoph und Kotlarz, Daniel (2019): CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel Disease. In: Inflammatory Bowel Diseases, Bd. 25, Nr. 11: S. 1788-1795

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

Li, Yue; Fuehrer, Marita; Bahrami, Ehsan; Socha, Piotr; Klaudel-Dreszler, Maja; Bouzidi, Amira; Liu, Yanshan; Lehle, Anna S.; Magg, Thomas; Hollizeck, Sebastian; Rohlfs, Meino; Conca, Raffaele; Field, Michael; Warner, Neil; Mordechai, Slae; Shteyer, Eyal; Turner, Dan; Boukari, Rachida; Belbouab, Reda; Walz, Christoph; Gaidt, Moritz M.; Hornung, Veit; Baumann, Bernd; Pannicke, Ulrich; Al Idrissi, Eman; Alghamdi, Hamza Ali; Sepulveda, Fernando E.; Gil, Marine; Basile, Genevieve de Saint; Honig, Manfred; Koletzko, Sibylle; Muise, Aleixo M.; Snapper, Scott B.; Schwarz, Klaus; Klein, Christoph und Kotlarz, Daniel (2019): Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases. In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 116, Nr. 3: S. 970-975

Magg, Thomas; Wiebking, Volker; Conca, Raffaele; Krebs, Stefan; Arens, Stefan; Schmid, Irene; Klein, Christoph; Albert, Michael H. und Hauck, Fabian (2018): IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective T-Reg cell engraftment. In: Clinical Immunology, Bd. 191: S. 52-58

Kotlarz, Daniel; Marquardt, Benjamin; Baroy, Tuva; Lee, Way S.; Konnikova, Liza; Hollizeck, Sebastian; Magg, Thomas; Lehle, Anna S.; Walz, Christoph; Borggraefe, Ingo; Hauck, Fabian; Bufler, Philip; Conca, Raffaele; Wall, Sarah M.; Schumacher, Eva M.; Misceo, Doriana; Frengen, Eirik; Bentsen, Beint S.; Uhlig, Holm H.; Hopfner, Karl-Peter; Muise, Aleixo M.; Snapper, Scott B.; Stromme, Petter und Klein, Christoph (2018): Human TGF-beta 1 deficiency causes severe inflammatory bowel disease and encephalopathy. In: Nature Genetics, Bd. 50, Nr. 3: S. 344-348

Frowein, Julia von; Hauck, Stefanie M.; Kappler, Roland; Pagel, Philipp; Fleischmann, Katrin K.; Magg, Thomas; Cairo, Stefano; Roscher, Adelbert; Schweinitz, Dietrich von und Schmid, Irene (2018): MiR‐492 regulates metastatic properties of hepatoblastoma via CD44. In: Liver International, Bd. 38, Nr. 7: S. 1280-1291

Magg, Thomas; Schober, Tilmann; Walz, Christoph; Ley-Zaporozhan, Julia; Facchetti, Fabio; Klein, Christoph und Hauck, Fabian (2018): Epstein–Barr Virus+ Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders. In: Frontiers in Immunology, Bd. 9, 368 [PDF, 567kB]

Hauck, Fabian; Magg, Thomas; Krolo, Ana; Bilic, Ivan; Hirschmugl, Tatjana; Laass, Martin; Rösen-Wolff, Angela; Luksch, Hella; Boztug, Kaan und Rösler, Joachim (2017): Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma. In: Klinische Pädiatrie, Bd. 229, Nr. 3: S. 113-117

Fleischmann, Katrin K.; Pagel, Philipp; Frowein, Julia von; Magg, Thomas; Roscher, Adelbert A. und Schmid, Irene (2016): The leukemogenic fusion gene MLL-AF9 alters microRNA expression pattern and inhibits monoblastic differentiation via miR-511 repression. In: Journal of Experimental & Clinical Cancer Research 35 [PDF, 1MB]

Hagl, Beate; Heinz, Valerie; Schlesinger, Anne; Spielberger, Benedikt D.; Sawalle-Belohradsky, Julie; Senn-Rauh, Monika; Magg, Thomas; Boos, Annette C.; Hönig, Manfred; Schwarz, Klaus; Dückers, Gregor; Bernuth, Horst von; Pache, Christoph; Karitnig-Weiss, Cäcilia; Belohradsky, Bernd H.; Frank, Josef; Niehues, Tim; Wahn, Volker; Albert, Michael H.; Wollenberg, Andreas; Jansson, Annette F. und Renner, Ellen D. (2016): Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children. In: Pediatric Allergy and Immunology, Bd. 27, Nr. 2: S. 177-184

Diese Liste wurde am Sat Mar 23 22:24:17 2024 CET erstellt.