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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 7

Zeitschriftenartikel

Osterman, Andreas; Badell, Irina; Dächert, Christopher; Schneider, Nikolas; Kaufmann, Anna-Yasemin; Öztan, Gamze Naz; Huber, Melanie; Späth, Patricia M.; Stern, Marcel; Autenrieth, Hanna; Muenchhoff, Maximilian; Graf, Alexander; Krebs, Stefan; Blum, Helmut; Czibere, Ludwig; Durner, Jürgen; Kaderali, Lars; Baldauf, Hanna-Mari und Keppler, Oliver T. ORCID logoORCID: https://orcid.org/0000-0002-1384-8946 (2022): Variable detection of Omicron-BA.1 and -BA.2 by SARS-CoV-2 rapid antigen tests. In: Medical Microbiology and Immunology, Bd. 212, Nr. 1: S. 13-23 [PDF, 1MB]

Durner, Juergen; Burggraf, Siegfried; Czibere, Ludwig; Tehrani, Arman; Watts, David C. und Becker, Marc (2021): Fast and cost-effective screening for SARS-CoV-2 variants in a routine diagnostic setting. In: Dental Materials, Bd. 37, Nr. 3, E95-E97

Vill, Katharina; Schwartz, Oliver; Blaschek, Astrid; Glaeser, Dieter; Nennstiel, Uta; Wirth, Brunhilde; Burggraf, Siegfried; Roeschinger, Wulf; Becker, Marc; Czibere, Ludwig; Durner, Jürgen; Eggermann, Katja; Olgemoeller, Bernhard; Harms, Erik; Schara, Ulrike; Koelbel, Heike und Mueller-Felber, Wolfgang (2021): Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years. In: Orphanet Journal of Rare Diseases, Bd. 16, Nr. 1, 153

Czibere, Ludwig; Burggraf, Siegfried; Fleige, Tobias; Glueck, Birgit; Keitel, Lisa Marie; Landt, Olfert; Durner, Jürgen; Roeschinger, Wulf; Hohenfellner, Katharina; Wirth, Brunhilde; Müller-Felber, Wolfgang; Vill, Katharina und Becker, Marc (2020): High-throughput genetic newborn screening for spinal muscular atrophy by rapid nucleic acid extraction from dried blood spots and 384-well qPCR. In: European Journal of Human Genetics, Bd. 28, Nr. 1: S. 23-30

Fleige, Tobias; Burggraf, Siegfried; Czibere, Ludwig; Haring, Julia; Glueck, Birgit; Keitel, Lisa Marie; Landt, Olfert; Harms, Erik; Hohenfellner, Katharina; Durner, Jürgen; Roeschinger, Wulf und Becker, Marc (2020): Next generation sequencing as second-tier test in high-throughput newborn screening for nephropathic cystinosis. In: European Journal of Human Genetics, Bd. 28, Nr. 2: S. 193-201

Hohenfellner, Katharina; Bergmann, Carsten; Fleige, Tobias; Janzen, Nils; Burggraf, Siegfried; Olgemoeller, Bernd; Gahl, William A.; Czibere, Ludwig; Froschauer, Sonja; Roeschinger, Wulf; Vill, Katharina; Harms, Erik und Nennstiel, Uta (2019): Molecular based newborn screening in Germany: Follow-up for cystinosis. In: Molecular Genetics and Metabolism Reports, Bd. 21, 100514

Czibere, Ludwig; Baur, Laura A.; Wittmann, Anke; Gemmeke, Katja; Steiner, Andrea; Weber, Peter; Pütz, Benno; Ahmad, Nafees; Bunck, Mirjam; Graf, Cornelia; Widner, Regina; Kühne, Claudia; Panhuysen, Markus; Hambsch, Boris; Rieder, Gabriele; Reinheckel, Thomas; Peters, Christoph; Holsboer, Florian; Landgraf, Rainer und Deussing, Jan M. (2011): Profiling trait anxiety: transcriptome analysis reveals cathepsin B (Ctsb) as a novel candidate gene for emotionality in mice.
In: PLOS ONE 7(8), e23604 [PDF, 512kB]

Diese Liste wurde am Sat Mar 16 18:32:26 2024 CET erstellt.