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Anzahl der Publikationen: 5
Zeitschriftenartikel
Shi, Yanyan; Strobl, Ralf 
ORCID: https://orcid.org/0000-0002-7719-948X; Apfelbacher, Christian; Bahmer, Thomas; Geisler, Ramsia; Heuschmann, Peter; Horn, Anna; Hoven, Hanno; Keil, Thomas; Krawczak, Michael; Krist, Lilian; Lemhöfer, Christina; Lieb, Wolfgang; Lorenz-Depiereux, Bettina; Mikolajczyk, Rafael; Montellano, Felipe A.; Reese, Jens Peter; Schreiber, Stefan; Skoetz, Nicole; Störk, Stefan; Vehreschild, Jörg Janne; Witzenrath, Martin und Grill, Eva ORCID: https://orcid.org/0000-0002-0273-7984
(Dezember 2023):
Persistent symptoms and risk factors predicting prolonged time to symptom-free after SARS‑CoV‑2 infection: an analysis of the baseline examination of the German COVIDOM/NAPKON-POP cohort.
In: Infection, Bd. 51: S. 1679-1694
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-7719-948X; Apfelbacher, Christian; Bahmer, Thomas; Geisler, Ramsia; Heuschmann, Peter; Horn, Anna; Hoven, Hanno; Keil, Thomas; Krawczak, Michael; Krist, Lilian; Lemhöfer, Christina; Lieb, Wolfgang; Lorenz-Depiereux, Bettina; Mikolajczyk, Rafael; Montellano, Felipe A.; Reese, Jens Peter; Schreiber, Stefan; Skoetz, Nicole; Störk, Stefan; Vehreschild, Jörg Janne; Witzenrath, Martin und Grill, Eva ORCID: https://orcid.org/0000-0002-0273-7984
(Dezember 2023):
Persistent symptoms and risk factors predicting prolonged time to symptom-free after SARS‑CoV‑2 infection: an analysis of the baseline examination of the German COVIDOM/NAPKON-POP cohort.
In: Infection, Bd. 51: S. 1679-1694
[PDF, 1MB]
Baumann, Tobias; Dunkel, Andreas; Schmid, Christian; Schmitt, Sabine; Hiltensperger, Michael; Lohr, Kerstin; Laketa, Vibor; Donakonda, Sainitin; Ahting, Uwe; Lorenz-Depiereux, Bettina; Heil, Jan E.; Schredelseker, Johann; Simeoni, Luca; Fecher, Caroline; Koerber, Nina; Bauer, Tanja; Hueser, Norbert; Hartmann, Daniel; Laschinger, Melanie; Eyerich, Kilian; Eyerich, Stefanie; Anton, Martina; Streeter, Matthew; Wang, Tina; Schraven, Burkhart; Spiegel, David; Assaad, Farhah; Misgeld, Thomas; Zischka, Hans; Murray, Peter J.; Heine, Annkristin; Heikenwaelder, Mathias; Korn, Thomas; Dawid, Corinna; Hofmann, Thomas; Knolle, Percy A. und Hoechst, Bastian
(2020):
Regulatory myeloid cells paralyze T cells through cell-cell transfer of the metabolite methylglyoxal.
In: Nature Immunology, Bd. 21, Nr. 5: S. 555-566
Fuchs, Helmut; Sabrautzki, Sibylle; Przemeck, Gerhard K. H.; Leuchtenberger, Stefanie; Lorenz-Depiereux, Bettina; Becker, Lore; Rathkolb, Birgit; Horsch, Marion; Garrett, Lillian; Östereicher, Manuela A.; Hans, Wolfgang; Abe, Koichiro; Sagawa, Nobuho; Rozman, Jan; Vargas-Panesso, Ingrid L.; Sandholzer, Michael; Lisse, Thomas S.; Adler, Thure; Aguilar-Pimentel, Juan Antonio; Calzada-Wack, Julia; Ehrhard, Nicole; Elvert, Ralf; Gau, Christine; Hölter, Sabine M.; Micklich, Katja; Moreth, Kristin; Prehn, Cornelia; Puk, Oliver; Racz, Ildiko; Stoeger, Claudia; Vernaleken, Alexandra; Michel, Dian; Diener, Susanne; Wieland, Thomas; Adamski, Jerzy; Bekeredjian, Raffi; Busch, Dirk H.; Favor, John; Graw, Jochen; Klingenspor, Martin; Lengger, Christoph; Maier, Holger; Neff, Frauke; Ollert, Markus; Stoeger, Tobias; Yildirim, Ali Önder; Strom, Tim M.; Zimmer, Andreas; Wolf, Eckhard; Wurst, Wolfgang; Klopstock, Thomas; Beckers, Johannes; Gailus-Durner, Valerie und Hrabé de Angelis, Martin
(2016):
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.
In: G3-Genes Genomes Genetics, Bd. 6, Nr. 12: S. 4035-4046
Sabrautzki, Sibylle; Sandholzer, Michael A.; Lorenz-Depiereux, Bettina; Brommage, Robert; Przemeck, Gerhard; Panesso, Ingrid L. Vargas; Vernaleken, Alexandra; Garrett, Lillian; Baron, Katharina; Yildirim, Ali O.; Rozman, Jan; Rathkolb, Birgit; Gau, Christine; Hans, Wolfgang; Hoelter, Sabine M.; Marschall, Susan; Stoeger, Claudia; Becker, Lore; Fuchs, Helmut; Gailus-Durner, Valerie; Klingenspor, Martin; Klopstock, Thomas; Lengger, Christoph; Stefanie, Leuchtenberger; Wolf, Eckhard; Strom, Tim M.; Wurst, Wolfgang und Hrabě de Angelis, Martin
(2016):
Viable Ednra (Y129F) mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.
In: Mammalian Genome, Bd. 27, Nr. 11-12: S. 587-598
Diener, Susanne; Bayer, Sieglinde; Sabrautzki, Sibylle; Wieland, Thomas; Mentrup, Birgit; Przemeck, Gerhard K. H.; Rathkolb, Birgit; Graf, Elisabeth; Hans, Wolfgang; Fuchs, Helmut; Horsch, Marion; Schwarzmayr, Thomas; Wolf, Eckhard; Klopocki, Eva; Jakob, Franz; Strom, Tim M.; Hrabě de Angelis, Martin und Lorenz-Depiereux, Bettina
(2016):
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
In: Mammalian Genome, Bd. 27, Nr. 3-4: S. 111-121