Sybille Bohm
Planegg, BY 82152, Germany
Last Updated: 09/26/2026
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Found 10 publications
mRNA trans-splicing dual AAV vectors for (epi)genome editing and gene therapy.
Journal: Nature communications
Published: August 17, 2022
dCas9-VPR-mediated transcriptional activation of functionally equivalent genes for gene therapy.
Journal: Nature protocols
Published: February 01, 2021
Antisense Oligonucleotide- and CRISPR-Cas9-Mediated Rescue of mRNA Splicing for a Deep Intronic CLRN1 Mutation.
Journal: Molecular therapy. Nucleic acids
Published: March 09, 2020
A gene therapy for inherited blindness using dCas9-VPR-mediated transcriptional activation.
Journal: Science advances
Published: December 13, 2019
Enigmatic rhodopsin mutation creates an exceptionally strong splice acceptor site.
Journal: Human molecular genetics
Published: September 23, 2019
Construction and Cloning of Minigenes for in vivo Analysis of Potential Splice Mutations.
Journal: Bio-protocol
Published: January 08, 2018
Peripherin-2 and Rom-1 have opposing effects on rod outer segment targeting of retinitis pigmentosa-linked peripherin-2 mutants.
Journal: Scientific reports
Published: January 19, 2017
AAV Vectors for FRET-Based Analysis of Protein-Protein Interactions in Photoreceptor Outer Segments.
AAV Vectors for FRET-Based Analysis of Protein-Protein Interactions in Photoreceptor Outer Segments.
Journal: Frontiers in neuroscience
Published: April 20, 2016
Peripherin-2 differentially interacts with cone opsins in outer segments of cone photoreceptors.
Journal: Human molecular genetics
Published: February 02, 2016
In Vivo Analysis of Disease-Associated Point Mutations Unveils Profound Differences in mRNA Splicing of Peripherin-2 in Rod and Cone Photoreceptors.
Journal: PLoS genetics
Published: August 27, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026