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 (11-20 of 196) with videos related to

Pageof 20
Sort By:
Molecular Vision|February 13, 2014
Homozygosity mapping reveals new nonsense mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in a Palestinian familyDitta Zobor, Ghassan Balousha, Britta Baumann, et al.
Histochemistry and Cell Biology|September 11, 2007
OPA1, the disease gene for optic atrophy type Kjer, is expressed in the inner earStefanie Bette, Ulrike Zimmermann, Bernd Wissinger, et al.
Human Mutation|August 28, 2007
Comprehensive cDNA study and quantitative transcript analysis of mutant OPA1 transcripts containing premature termination codonsSimone Schimpf, Nico Fuhrmann, Simone Schaich, et al.
Molecular Pharmacology|April 8, 2021
Identification of Chemical and Pharmacological Chaperones for Correction of Trafficking-Deficient Mutant Cyclic Nucleotide-Gated A3 ChannelsJoachim Täger, Bernd Wissinger, Susanne Kohl, et al.
Experimental Eye Research|August 1, 2007
Identification of genes that are linked with optineurin expression using a combined RNAi--microarray approachNicole Weisschuh, Marcel V Alavi, Michael Bonin, et al.
BMC Medical Genetics|June 27, 2018
A 73,128 bp de novo deletion encompassing the OPN1LW/OPN1MW gene cluster in sporadic Blue Cone Monochromacy: a case reportElena Buena-Atienza, Fadi Nasser, Susanne Kohl, et al.
Molecular Vision|April 27, 2005
Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patientsNicole Weisschuh, Dorit Neumann, Christiane Wolf, et al.
Acta Neuropathologica|February 9, 2005
OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brainStefanie Bette, Holger Schlaszus, Bernd Wissinger, et al.
Molecular Vision|December 2, 2005
Clinical and genetic features of Hungarian achromatopsia patientsBalázs Varsányi, Bernd Wissinger, Susanne Kohl, et al.
Investigative Ophthalmology & Visual Science|July 27, 2007
CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated functionNaheed Wali Khan, Bernd Wissinger, Susanne Kohl, et al.
Pageof 20

Showing results (11-20 of 196) with videos related to

Sort By:
Pageof 20
Molecular Vision|February 13, 2014
Homozygosity mapping reveals new nonsense mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in a Palestinian familyDitta Zobor, Ghassan Balousha, Britta Baumann, et al.
Histochemistry and Cell Biology|September 11, 2007
OPA1, the disease gene for optic atrophy type Kjer, is expressed in the inner earStefanie Bette, Ulrike Zimmermann, Bernd Wissinger, et al.
Human Mutation|August 28, 2007
Comprehensive cDNA study and quantitative transcript analysis of mutant OPA1 transcripts containing premature termination codonsSimone Schimpf, Nico Fuhrmann, Simone Schaich, et al.
Molecular Pharmacology|April 8, 2021
Identification of Chemical and Pharmacological Chaperones for Correction of Trafficking-Deficient Mutant Cyclic Nucleotide-Gated A3 ChannelsJoachim Täger, Bernd Wissinger, Susanne Kohl, et al.
Experimental Eye Research|August 1, 2007
Identification of genes that are linked with optineurin expression using a combined RNAi--microarray approachNicole Weisschuh, Marcel V Alavi, Michael Bonin, et al.
BMC Medical Genetics|June 27, 2018
A 73,128 bp de novo deletion encompassing the OPN1LW/OPN1MW gene cluster in sporadic Blue Cone Monochromacy: a case reportElena Buena-Atienza, Fadi Nasser, Susanne Kohl, et al.
Molecular Vision|April 27, 2005
Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patientsNicole Weisschuh, Dorit Neumann, Christiane Wolf, et al.
Acta Neuropathologica|February 9, 2005
OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brainStefanie Bette, Holger Schlaszus, Bernd Wissinger, et al.
Molecular Vision|December 2, 2005
Clinical and genetic features of Hungarian achromatopsia patientsBalázs Varsányi, Bernd Wissinger, Susanne Kohl, et al.
Investigative Ophthalmology & Visual Science|July 27, 2007
CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated functionNaheed Wali Khan, Bernd Wissinger, Susanne Kohl, et al.
Pageof 20