Dirk Grimm
Affiliations: | Heidelberg University Hospital |
Area:
RNAi, gene therapy, AAV, iPS cells, genome engineeringGoogle:
"Dirk Grimm"Parents
Sign in to add mentor| Jürgen A. Kleinschmidt | grad student | Deutschen Krebsforschungszentrums | |
| Mark A. Kay | post-doc | Stanford |
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Publications
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| Theuerkauf SA, Herrera-Carrillo E, John F, et al. (2023) AAV vectors displaying bispecific DARPins enable dual-control targeted gene delivery. Biomaterials. 303: 122399 |
| Liu J, Koay TW, Maiakovska O, et al. (2023) Progress in Bioengineering of Myotropic Adeno-Associated Viral Gene Therapy Vectors. Human Gene Therapy. 34: 350-364 |
| Rapti K, Maiakovska O, Becker J, et al. (2022) Isolation of Next-Generation Gene Therapy Vectors through Engineering, Barcoding, and Screening of Adeno-Associated Virus (AAV) Capsid Variants. Journal of Visualized Experiments : Jove |
| Szumska J, Grimm D. (2022) Boosters for adeno-associated virus vector (AAV) (r)evolution. Cytotherapy |
| Becker J, Fakhiri J, Grimm D. (2022) Fantastic AAV Gene Therapy Vectors and How to Find Them-Random Diversification, Rational Design and Machine Learning. Pathogens (Basel, Switzerland). 11 |
| Mann AM, Schäfer W, Adriouch S, et al. (2022) Enhanced Transduction of P2X7-Expressing Cells with Recombinant rAAV Vectors. Methods in Molecular Biology (Clifton, N.J.). 2510: 129-144 |
| Gadenstaetter AJ, Schmutzler L, Grimm D, et al. (2022) Intranasal application of adeno-associated viruses: a systematic review. Translational Research : the Journal of Laboratory and Clinical Medicine |
| Becker J, Stanifer ML, Leist SR, et al. (2022) Ex vivo and in vivo suppression of SARS-CoV-2 with combinatorial AAV-RNAi expression vectors. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Michels A, Frank AM, Günther DM, et al. (2021) Lentiviral and adeno-associated vectors efficiently transduce mouse T lymphocytes when targeted to murine CD8. Molecular Therapy. Methods & Clinical Development. 23: 334-347 |
| Zhang C, Freistaedter A, Schmelas C, et al. (2021) An RNA Interference/Adeno-Associated Virus Vector-Based Combinatorial Gene Therapy Approach Against Hepatitis E Virus. Hepatology Communications |