Hasil Pencarian - Dominik Wrona
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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 2019-06-01
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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 2020-06-01
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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 2024-10-01
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