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Molecular Therapy : the Journal of the American Society of Gene Therapy|November 28, 2012
Minicircle DNA vectors achieve sustained expression reflected by active chromatin and transcriptional levelLia E Gracey Maniar, Jay M Maniar, Zhi-Ying Chen, et al.
Nature|July 5, 2002
RNA interference in adult miceAnton P McCaffrey, Leonard Meuse, Thu-Thao T Pham, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 23, 2006
Robust systemic transduction with AAV9 vectors in mice: efficient global cardiac gene transfer superior to that of AAV8Katsuya Inagaki, Sally Fuess, Theresa A Storm, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 9, 2026
Distinct YY dinucleotide periodicity in Adeno-associated virus (AAV) DNAConradin Baumgartl, Jonas Becker, Lena Naber, et al.
Molecular Systems Biology|July 8, 2015
T160‐phosphorylated CDK2 defines threshold for HGF dependent proliferation in primary hepatocytesStephanie Mueller, Jérémy Huard, Katharina Waldow, et al.
Nucleic Acids Research|April 16, 2019
Cell-specific CRISPR-Cas9 activation by microRNA-dependent expression of anti-CRISPR proteinsMareike D Hoffmann, Sabine Aschenbrenner, Stefanie Grosse, et al.
Nature|March 10, 2022
Methane formation driven by reactive oxygen species across all living organismsLeonard Ernst, Benedikt Steinfeld, Uladzimir Barayeu, et al.
Epigenetics & Chromatin|July 3, 2010
An in vitro-identified high-affinity nucleosome-positioning signal is capable of transiently positioning a nucleosome in vivoLia E Gracey, Zhi-Ying Chen, Jay M Maniar, et al.
Nucleic Acids Research|December 17, 2020
Optogenetic control of Neisseria meningitidis Cas9 genome editing using an engineered, light-switchable anti-CRISPR proteinMareike D Hoffmann, Jan Mathony, Julius Upmeier Zu Belzen, et al.
Glia|November 10, 2017
Synthetic AAV/CRISPR vectors for blocking HIV-1 expression in persistently infected astrocytesChristine Kunze, Kathleen Börner, Eike Kienle, et al.
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