Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bernd Wissinger

Showing results (41-50 of 196) with videos related to

Pageof 20
Sort By:
Cells|March 29, 2023
In Vivo Efficacy and Safety Evaluations of Therapeutic Splicing Correction Using U1 snRNA in the Mouse RetinaSebastian Swirski, Oliver May, Malte Ahlers, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Electrophysiological and histologic assessment of retinal ganglion cell fate in a mouse model for OPA1-associated autosomal dominant optic atrophyPeter Heiduschka, Sven Schnichels, Nico Fuhrmann, et al.
Journal of Glaucoma|April 18, 2009
Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucomaChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
Ophthalmic Genetics|July 7, 2011
Cone-rod dystrophy associated with amelogenesis imperfecta in a child with neurofibromatosis type 1Ditta Zobor, Dieter H Kaufmann, Petra Weckerle, et al.
Ophthalmic Genetics|July 21, 2021
Visual and ocular findings in a family with X-linked cone dysfunction and protanopiaDag Holmquist, David Epstein, Monica Olsson, et al.
Experimental Eye Research|March 3, 2018
An early nonsense mutation facilitates the expression of a short isoform of CNGA3 by alternative translation initiationJoachim Täger, Susanne Kohl, David G Birch, et al.
Molecular Therapy. Nucleic Acids|November 23, 2016
Antisense Oligonucleotide Mediated Splice Correction of a Deep Intronic Mutation in OPA1Tobias Bonifert, Irene Gonzalez Menendez, Florian Battke, et al.
BMC Medical Genetics|September 17, 2009
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control studyChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
International Journal of Molecular Sciences|June 2, 2021
Clinical Characteristics of <i>POC1B</i>-Associated Retinopathy and Assignment of Pathogenicity to Novel Deep Intronic and Non-Canonical Splice Site VariantsNicole Weisschuh, Pascale Mazzola, Miriam Bertrand, et al.
Molecular Therapy. Nucleic Acids|August 22, 2022
Effective splicing restoration of a deep-intronic <i>ABCA4</i> variant in cone photoreceptor precursor cells by CRISPR/<i>Sp</i>Cas9 approachesPietro De Angeli, Peggy Reuter, Stefan Hauser, et al.
Pageof 20

Showing results (41-50 of 196) with videos related to

Sort By:
Pageof 20
Cells|March 29, 2023
In Vivo Efficacy and Safety Evaluations of Therapeutic Splicing Correction Using U1 snRNA in the Mouse RetinaSebastian Swirski, Oliver May, Malte Ahlers, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Electrophysiological and histologic assessment of retinal ganglion cell fate in a mouse model for OPA1-associated autosomal dominant optic atrophyPeter Heiduschka, Sven Schnichels, Nico Fuhrmann, et al.
Journal of Glaucoma|April 18, 2009
Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucomaChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
Ophthalmic Genetics|July 7, 2011
Cone-rod dystrophy associated with amelogenesis imperfecta in a child with neurofibromatosis type 1Ditta Zobor, Dieter H Kaufmann, Petra Weckerle, et al.
Ophthalmic Genetics|July 21, 2021
Visual and ocular findings in a family with X-linked cone dysfunction and protanopiaDag Holmquist, David Epstein, Monica Olsson, et al.
Experimental Eye Research|March 3, 2018
An early nonsense mutation facilitates the expression of a short isoform of CNGA3 by alternative translation initiationJoachim Täger, Susanne Kohl, David G Birch, et al.
Molecular Therapy. Nucleic Acids|November 23, 2016
Antisense Oligonucleotide Mediated Splice Correction of a Deep Intronic Mutation in OPA1Tobias Bonifert, Irene Gonzalez Menendez, Florian Battke, et al.
BMC Medical Genetics|September 17, 2009
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control studyChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
International Journal of Molecular Sciences|June 2, 2021
Clinical Characteristics of <i>POC1B</i>-Associated Retinopathy and Assignment of Pathogenicity to Novel Deep Intronic and Non-Canonical Splice Site VariantsNicole Weisschuh, Pascale Mazzola, Miriam Bertrand, et al.
Molecular Therapy. Nucleic Acids|August 22, 2022
Effective splicing restoration of a deep-intronic <i>ABCA4</i> variant in cone photoreceptor precursor cells by CRISPR/<i>Sp</i>Cas9 approachesPietro De Angeli, Peggy Reuter, Stefan Hauser, et al.
Pageof 20