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Bernd Wissinger

Showing results (71-80 of 196) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2004
Molecular basis of an inherited form of incomplete achromatopsiaDimitri Tränkner, Herbert Jägle, Susanne Kohl, et al.
Scientific Reports|February 2, 2023
Extra-viral DNA in adeno-associated viral vector preparations induces TLR9-dependent innate immune responses in human plasmacytoid dendritic cellsKirsten Bucher, Eduardo Rodríguez-Bocanegra, Bernd Wissinger, et al.
American Journal of Ophthalmology|June 23, 2024
Clinical and Genetic Findings in a Cohort of Patients with PRPF31-Associated Retinal DystrophyJan-Philipp Bodenbender, Leon Bethge, Katarina Stingl, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 2, 2011
GDF-15: a novel serum marker for metastases in uveal melanoma patientsDaniela Suesskind, Andreas Schatz, Sven Schnichels, et al.
American Journal of Ophthalmology|November 29, 2008
Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutationsAgnes B Renner, Britta S Fiebig, Bernhard H F Weber, et al.
Human Mutation|May 22, 2009
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclaseVeronique B D Kitiratschky, Petra Behnen, Ulrich Kellner, et al.
Molecular Therapy. Nucleic Acids|April 16, 2025
Single-guide RNA Cas9 and enhanced-deletion Cas9 rescue a recurrent <i>USH2A</i>-related splicing defectPietro De Angeli, Salome Spaag, Stefanida Shliaga, et al.
Investigative Ophthalmology & Visual Science|August 6, 2025
Flavoprotein Fluorescence Imaging in Stargardt Disease: Linking Metabolic Stress to Structural DamageDavid A Merle, Veronica Cuevas Villanueva, Giulia Righetti, et al.
Scientific Reports|August 3, 2017
CDHR1 mutations in retinal dystrophiesKatarina Stingl, Anja K Mayer, Pablo Llavona, et al.
Genes|October 21, 2017
Allelic Expression Imbalance in the Human Retinal Transcriptome and Potential Impact on Inherited Retinal DiseasesPablo Llavona, Michele Pinelli, Margherita Mutarelli, et al.
Pageof 20

Showing results (71-80 of 196) with videos related to

Sort By:
Pageof 20
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2004
Molecular basis of an inherited form of incomplete achromatopsiaDimitri Tränkner, Herbert Jägle, Susanne Kohl, et al.
Scientific Reports|February 2, 2023
Extra-viral DNA in adeno-associated viral vector preparations induces TLR9-dependent innate immune responses in human plasmacytoid dendritic cellsKirsten Bucher, Eduardo Rodríguez-Bocanegra, Bernd Wissinger, et al.
American Journal of Ophthalmology|June 23, 2024
Clinical and Genetic Findings in a Cohort of Patients with PRPF31-Associated Retinal DystrophyJan-Philipp Bodenbender, Leon Bethge, Katarina Stingl, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 2, 2011
GDF-15: a novel serum marker for metastases in uveal melanoma patientsDaniela Suesskind, Andreas Schatz, Sven Schnichels, et al.
American Journal of Ophthalmology|November 29, 2008
Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutationsAgnes B Renner, Britta S Fiebig, Bernhard H F Weber, et al.
Human Mutation|May 22, 2009
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclaseVeronique B D Kitiratschky, Petra Behnen, Ulrich Kellner, et al.
Molecular Therapy. Nucleic Acids|April 16, 2025
Single-guide RNA Cas9 and enhanced-deletion Cas9 rescue a recurrent <i>USH2A</i>-related splicing defectPietro De Angeli, Salome Spaag, Stefanida Shliaga, et al.
Investigative Ophthalmology & Visual Science|August 6, 2025
Flavoprotein Fluorescence Imaging in Stargardt Disease: Linking Metabolic Stress to Structural DamageDavid A Merle, Veronica Cuevas Villanueva, Giulia Righetti, et al.
Scientific Reports|August 3, 2017
CDHR1 mutations in retinal dystrophiesKatarina Stingl, Anja K Mayer, Pablo Llavona, et al.
Genes|October 21, 2017
Allelic Expression Imbalance in the Human Retinal Transcriptome and Potential Impact on Inherited Retinal DiseasesPablo Llavona, Michele Pinelli, Margherita Mutarelli, et al.
Pageof 20