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Showing 1–21 of 21 results

Advanced filters: Author: Eberhart Zrenner Clear advanced filters

Is colour vision possible with only rods and blue-sensitive cones?

Andreas Reitner
Lindsay T. Sharpe
Eberhart Zrenner
Research29 Aug 1991
Nature

Volume: 352, P: 798-800
Mutations in RPE65 cause Leber's congenital amaurosis

Françoise Marlhens
Corinne Bareil
Christian P. Hamel
Correspondence01 Oct 1997
Nature Genetics

Volume: 17, P: 139-141
Solar cells for the blind

Electronic implants have been used to restore visual function lost as a result of retinal degeneration. Combining subretinal high-pixel-density arrays with optically powered serial photovoltaic sensors may alleviate some of the difficulties associated with today's devices, which rely on implanted arrays and inductive coils.

Eberhart Zrenner
News & Views29 May 2012
Nature Photonics

Volume: 6, P: 344-345
New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis

Mathias W. Seeliger
Christian Grimm
Andreas Wenzel
Research20 Aug 2001
Nature Genetics

Volume: 29, P: 70-74
Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

Susanne Kohl
Tim Marx
Bernd Wissinger
Research01 Jul 1998
Nature Genetics

Volume: 19, P: 257-259
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Tim M. Strom
Gerald Nyakatura
Alfons Meindl
Research01 Jul 1998
Nature Genetics

Volume: 19, P: 260-263
Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies

Nicola Glöckle
Susanne Kohl
John Neidhardt
Research17 Apr 2013
European Journal of Human Genetics

Volume: 22, P: 99-104
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

Susanne Kohl
Balazs Varsanyi
Bernd Wissinger
Research15 Dec 2004
European Journal of Human Genetics

Volume: 13, P: 302-308
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina

Krisztina Wutz
Christian Sauer
Carsten M Pusch
Research16 Jul 2002
European Journal of Human Genetics

Volume: 10, P: 449-456
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

Susanne Kohl and colleagues report mutations in ATF6, a regulator of the unfolded protein response pathway, that cause a familial form of achromatopsia. Their results indicate a role for ATF6 in foveal development rather than a direct role in the cone phototransduction pathway.

Susanne Kohl
Ditta Zobor
Jonathan H Lin
Research01 Jun 2015
Nature Genetics

Volume: 47, P: 757-765
Bioengineering strategies for restoring vision

This Review discusses the most promising gene therapies, cell therapies and retinal prostheses for the treatment of retinal degeneration, as well as upcoming technologies for enhancing vision restoration.

Jasmina Cehajic-Kapetanovic
Mandeep S. Singh
Robert E. MacLaren
Reviews31 Jan 2022
Nature Biomedical Engineering

Volume: 7, P: 387-404
Non-invasive measuring of biopotentials of the ciliary muscle during accommodation in emmetropes

Sven Schumayer
Bishesh Sigdel
Sandra Wagner
ResearchOpen Access03 Jun 2025
Scientific Reports

Volume: 15, P: 1-12
Decreased Na⁺/K⁺ ATPase Expression and Depolarized Cell Membrane in Neurons Differentiated from Chorea-Acanthocytosis Patients

Zohreh Hosseinzadeh
Stefan Hauser
Florian Lang
ResearchOpen Access21 May 2020
Scientific Reports

Volume: 10, P: 1-10
The perception threshold of the panda illusion, a particular form of 2D pulse-width-modulated halftone, correlates with visual acuity

Torsten Straßer
Anne Kurtenbach
Eberhart Zrenner
ResearchOpen Access04 Aug 2020
Scientific Reports

Volume: 10, P: 1-12
Electrical activation of degenerated photoreceptors in blind mouse retina elicited network-mediated responses in different types of ganglion cells

Wadood Haq
Johannes Dietter
Eberhart Zrenner
ResearchOpen Access19 Nov 2018
Scientific Reports

Volume: 8, P: 1-11
HDAC inhibition ameliorates cone survival in retinitis pigmentosa mice

Marijana Samardzija
Andrea Corna
Dragana Trifunović
ResearchOpen Access06 Nov 2020
Cell Death & Differentiation

Volume: 28, P: 1317-1332
Poly ADP ribosylation and extracellular vesicle activity in rod photoreceptor degeneration

Lorena Vidal-Gil
Javier Sancho-Pelluz
Ayse Sahaboglu
ResearchOpen Access06 Mar 2019
Scientific Reports

Volume: 9, P: 1-10
CDHR1 mutations in retinal dystrophies

Katarina Stingl
Anja K. Mayer
Nicole Weisschuh
ResearchOpen Access01 Aug 2017
Scientific Reports

Volume: 7, P: 1-11
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies

Veronique B D Kitiratschky
Tanja Grau
Bernd Wissinger
Research20 Feb 2008
European Journal of Human Genetics

Volume: 16, P: 812-819
Olaparib significantly delays photoreceptor loss in a model for hereditary retinal degeneration

Ayse Sahaboglu
Melanie Barth
François Paquet-Durand
ResearchOpen Access22 Dec 2016
Scientific Reports

Volume: 6, P: 1-11
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Crystel Bonnet
Zied Riahi
Christine Petit
ResearchOpen Access27 Jul 2016
European Journal of Human Genetics

Volume: 24, P: 1730-1738

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Search

Is colour vision possible with only rods and blue-sensitive cones?

Mutations in RPE65 cause Leber's congenital amaurosis

Solar cells for the blind

New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

Bioengineering strategies for restoring vision

Non-invasive measuring of biopotentials of the ciliary muscle during accommodation in emmetropes

Decreased Na⁺/K⁺ ATPase Expression and Depolarized Cell Membrane in Neurons Differentiated from Chorea-Acanthocytosis Patients

The perception threshold of the panda illusion, a particular form of 2D pulse-width-modulated halftone, correlates with visual acuity

Electrical activation of degenerated photoreceptors in blind mouse retina elicited network-mediated responses in different types of ganglion cells

HDAC inhibition ameliorates cone survival in retinitis pigmentosa mice

Poly ADP ribosylation and extracellular vesicle activity in rod photoreceptor degeneration

CDHR1 mutations in retinal dystrophies

ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies

Olaparib significantly delays photoreceptor loss in a model for hereditary retinal degeneration

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Search

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