Programmable RNA editing with endogenous ADAR enzymes – a feasible option for the treatment of inherited retinal disease?
Bellingrath J-S. et al, (2023), Frontiers in Molecular Neuroscience, 16
Envisioning the development of a CRISPR-Cas mediated base editing strategy for a patient with a novel pathogenic CRB1 single nucleotide variant.
Bellingrath J-S. et al, (2022), Ophthalmic Genet, 1 - 10
In Silico Analysis of Pathogenic CRB1 Single Nucleotide Variants and Their Amenability to Base Editing as a Potential Lead for Therapeutic Intervention.
Bellingrath J-S. et al, (2021), Genes (Basel), 12
Laparoscopic liver resection in caroli disease: A single-centre case series
Schoening W. et al, (2020), Journal of Minimal Access Surgery, 0, 0 - 0
Minimally Invasive Liver Surgery in Elderly Patients—A Single-Center Experience
Wabitsch S. et al, (2019), Journal of Surgical Research, 239, 92 - 97
High Symmetry of Visual Acuity and Visual Fields in RPGR-Linked Retinitis Pigmentosa
Bellingrath J-S. et al, (2017), Investigative Opthalmology & Visual Science, 58, 4457 - 4457
Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis Pigmentosa
Fischer MD. et al, (2017), Molecular Therapy, 25, 1854 - 1865
Gentherapie als Behandlungskonzept für erbliche Netzhauterkrankungen
Bellingrath J-S. and Fischer MD., (2015), Der Ophthalmologe, 112, 720 - 727