Hasil Pencarian - Ulrich Siler
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Novel Diagnostic Tool for p47phox-Deficient Chronic Granulomatous Disease Patient and Carrier Detection oleh Dominik Wrona, Ulrich Siler, Janine Reichenbach
Diterbitkan 2019-06-01Dapatkan teks lengkap
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CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions oleh Dominik Wrona, Oleksandr Pastukhov, Robert S. Pritchard, Federica Raimondi, Joëlle Tchinda, Martin Jinek, Ulrich Siler, Janine Reichenbach
Diterbitkan 2020-06-01Dapatkan teks lengkap
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High Levels of IL-18 and IFN-γ in Chronically Inflamed Tissue in Chronic Granulomatous Disease oleh Virginia Meda Spaccamela, Virginia Meda Spaccamela, Rocio G. Valencia, Oleksandr Pastukhov, Oleksandr Pastukhov, Andrea Duppenthaler, Matthias S. Dettmer, Juliane Erb, Urs C. Steiner, Sven Hillinger, Carsten Speckmann, Carsten Speckmann, Stephan Ehl, Stephan Ehl, Janine Reichenbach, Janine Reichenbach, Janine Reichenbach, Janine Reichenbach, Ulrich Siler, Ulrich Siler
Diterbitkan 2019-10-01Dapatkan teks lengkap
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Gene editing of NCF1 loci is associated with homologous recombination and chromosomal rearrangements oleh Federica Raimondi, Kah Mun Siow, Dominik Wrona, Carla Fuster-García, Oleksandr Pastukhov, Michael Schmitz, Katja Bargsten, Lucas Kissling, Daan C. Swarts, Geoffroy Andrieux, Toni Cathomen, Ute Modlich, Martin Jinek, Ulrich Siler, Janine Reichenbach
Diterbitkan 2024-10-01Dapatkan teks lengkap
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