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Anzahl der Publikationen: 4
Zeitschriftenartikel
Aparicio-Soto, Marina; Riedel, Franziska; Leddermann, Melanie; Bacher, Petra; Scheffold, Alexander; Kuhl, Heiner; Timmermann, Bernd; Chudakov, Dmitriy M.; Molin, Sonja; Worm, Margitta; Heine, Guido; Thierse, Hermann-Josef; Luch, Andreas und Siewert, Katherina
(2020):
TCRs with segment TRAV9-2 or a CDR3 histidine are overrepresented among nickel-specific CD4+T cells.
In: Allergy, Bd. 75, Nr. 10: S. 2574-2586
Segal, Joanna; Muelleder, Michael; Krüger, Antje; Adler, Thure; Scholze-Wittler, Manuela; Becker, Lore; Calzada-Wack, Julia; Garrett, Lillian; Hoelter, Sabine M.; Rathkolb, Birgit; Rozman, Jan; Racz, Ildiko; Fischer, Ralf; Busch, Dirk H.; Neff, Frauke; Klingenspor, Martin; Klopstock, Thomas; Grüning, Nana-Maria; Michel, Steve; Lukaszewska-McGreal, Beata; Voigt, Ingo; Hartmann, Ludger; Timmermann, Bernd; Lehrach, Hans; Wolf, Eckhard; Wurst, Wolfgang; Gailus-Durner, Valerie; Fuchs, Helmut; de Angelis, Martin H.; Schrewe, Heinrich; Yuneva, Mariia und Ralser, Markus
(2019):
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency.
In: Journal of Inherited Metabolic Disease, Bd. 42, Nr. 5: S. 839-849
[PDF, 3MB]
Spier, Isabel; Kerick, Martin; Drichel, Dmitriy; Horpaopan, Sukanya; Altmüller, Janine; Laner, Andreas; Holzapfel, Stefanie; Peters, Sophia; Adam, Ronja; Zhao, Bixiao; Becker, Tim; Lifton, Richard P.; Holinski-Feder, Elke; Perner, Sven; Thiele, Holger; Nöthen, Markus M.; Hoffmann, Per; Timmermann, Bernd; Schweiger, Michal R. und Aretz, Stefan
(2016):
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
In: Familial Cancer, Bd. 15, Nr. 2: S. 281-288
Spier, Isabel; Drichel, Dmitriy; Kerick, Martin; Kirfel, Jutta; Horpaopan, Sukanya; Laner, Andreas; Holzapfel, Stefanie; Peters, Sophia; Adam, Ronja; Zhao, Bixiao; Becker, Tim; Lifton, Richard P.; Perner, Sven; Hoffmann, Per; Kristiansen, Glen; Timmermann, Bernd; Nöthen, Markus M.; Holinski-Feder, Elke; Schweiger, Michal R. und Aretz, Stefan
(2016):
Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
In: Journal of Medical Genetics, Bd. 53, Nr. 3: S. 172-179
[PDF, 1MB]