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Cone loss is delayed relative to rod loss during induced retinal degeneration in the diurnal cone-rich rodent Arvicanthis ansorgei

Neuroscience, 2010-09, Vol.169 (4), p.1815-1830

2010

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Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice

Cellular and molecular life sciences : CMLS, 2010-09, Vol.67 (18), p.3173-3186

2010

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Bone spicule pigment formation in retinitis pigmentosa: insights from a mouse model

Graefe's archive for clinical and experimental ophthalmology, 2010-08, Vol.248 (8), p.1063-1070

2010

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Gene replacement therapy in achromatopsia type 2

Klinische Monatsblatter fur Augenheilkunde, 2014-03, Vol.231 (3), p.232

2014

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Synaptic vesicle alterations in rod photoreceptors of synaptophysin-deficient mice

Neuroscience, 2001-01, Vol.107 (1), p.127-142

2001

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Multifocal electroretinography in patients with Stargardt’s macular dystrophy

British journal of ophthalmology, 1998-03, Vol.82 (3), p.267-275

1998

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Prevention of Photoreceptor Apoptosis by Activation of the Glucocorticoid Receptor

Investigative ophthalmology & visual science, 2001-06, Vol.42 (7), p.1653-1659

2001

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Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis

Investigative ophthalmology & visual science, 1999-01, Vol.40 (1), p.3-11

1999

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Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein

The American journal of clinical nutrition, 1999-05, Vol.69 (5), p.931-936

1999

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In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopy

Vision research (Oxford), 2005-12, Vol.45 (28), p.3512-3519

2005

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Long-term engraftment of systemically transplanted, gene-modified bone marrow-derived cells in the adult mouse retina

British journal of ophthalmology, 2008-02, Vol.92 (2), p.272-275

2008

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Gene Replacement Therapy for Inherited Retinal Dystrophies

Klinische Monatsblatter fur Augenheilkunde, 2017-03, Vol.234 (3), p.320

2017

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In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death

Human molecular genetics, 2009-04, Vol.18 (7), p.1266-1275

2009

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Genetic Disorders of Vision Revealed by a Behavioral Screen of 400 Essential Loci in Zebrafish

The Journal of neuroscience, 1999-10, Vol.19 (19), p.8603-8615

1999

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Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors

Molecular vision, 2011, Vol.17, p.2934-2946

2011

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Implicit time topography of multifocal electroretinograms

Investigative ophthalmology & visual science, 1998-04, Vol.39 (5), p.718-723

1998

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Functional Assessment of the Regional Distribution of Disease in a Cat Model of Hereditary Retinal Degeneration

Investigative ophthalmology & visual science, 2000-06, Vol.41 (7), p.1998-2005

2000

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

Nature genetics, 2001-09, Vol.29 (1), p.70-74

2001

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Inactivation of the Murine X-Linked Juvenile Retinoschisis Gene, Rs1h, Suggests a Role of Retinoschisin in Retinal Cell Layer Organization and Synaptic Structure

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (9), p.6222-6227

2002

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Knockout of PARG110 confers resistance to cGMP-induced toxicity in mammalian photoreceptors

Cell death & disease, 2014-05, Vol.5 (5), p.e1234-e1234

2014

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Identification of Usher Syndrome Subtypes by ERG Implicit Time

Investigative ophthalmology & visual science, 2001-11, Vol.42 (12), p.3066-3071

2001

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cGMP-Dependent Protein Kinase II Modulates mPer1 and mPer2 Gene Induction and Influences Phase Shifts of the Circadian Clock

Current biology, 2003-04, Vol.13 (9), p.725-733

2003

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Genersatztherapie bei hereditären Netzhauterkrankungen

Klinische Monatsblätter für Augenheilkunde, 2017-03, Vol.234 (3), p.320-328

2017

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In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death

Human molecular genetics, 2011-02, Vol.20 (3), p.628-628

2011

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Genersatztherapie bei genetisch bedingter Zapfenblindheit

Klinische Monatsblätter für Augenheilkunde, 2014-03, Vol.231 (3), p.232-240

2014

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Cone loss is delayed relative to rod loss during induced retinal degeneration in the diurnal cone-rich rodent Arvicanthis ansorgei

Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice

Bone spicule pigment formation in retinitis pigmentosa: insights from a mouse model

Gene replacement therapy in achromatopsia type 2

Synaptic vesicle alterations in rod photoreceptors of synaptophysin-deficient mice

Multifocal electroretinography in patients with Stargardt’s macular dystrophy

Prevention of Photoreceptor Apoptosis by Activation of the Glucocorticoid Receptor

Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis

Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein

In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopy

Long-term engraftment of systemically transplanted, gene-modified bone marrow-derived cells in the adult mouse retina

Gene Replacement Therapy for Inherited Retinal Dystrophies

In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death

Genetic Disorders of Vision Revealed by a Behavioral Screen of 400 Essential Loci in Zebrafish

Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors

Implicit time topography of multifocal electroretinograms

Functional Assessment of the Regional Distribution of Disease in a Cat Model of Hereditary Retinal Degeneration

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

Inactivation of the Murine X-Linked Juvenile Retinoschisis Gene, Rs1h, Suggests a Role of Retinoschisin in Retinal Cell Layer Organization and Synaptic Structure

Knockout of PARG110 confers resistance to cGMP-induced toxicity in mammalian photoreceptors

Identification of Usher Syndrome Subtypes by ERG Implicit Time

cGMP-Dependent Protein Kinase II Modulates mPer1 and mPer2 Gene Induction and Influences Phase Shifts of the Circadian Clock

Genersatztherapie bei hereditären Netzhauterkrankungen

In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death

Genersatztherapie bei genetisch bedingter Zapfenblindheit

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