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Deficiency in Lyst function leads to accumulation of secreted proteases and reduced retinal adhesion

PloS one, 2022-03, Vol.17 (3), p.e0254469

2022

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Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10419

2022

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Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model

PLoS genetics, 2022-06, Vol.18 (6), p.e1009798

2022

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Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes

International journal of molecular sciences, 2022-01, Vol.23 (3), p.1615

2022

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NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

Human molecular genetics, 2011-02, Vol.20 (3), p.482-496

2011

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Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Journal of neurophysiology, 2012-11, Vol.108 (9), p.2442-2451

2012

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Degradation of IRS1 leads to impaired glucose uptake in adipose tissue of the type 2 diabetes mouse model TALLYHO/Jng

Journal of endocrinology, 2009-10, Vol.203 (1), p.65-74

2009

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Epithelial mechanics are maintained by inhibiting cell fusion with age in Drosophila

Journal of cell science, 2023-10, Vol.136 (20)

2023

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Mouse Model Resources for Vision Research

Journal of ophthalmology, 2011-01, Vol.2011, p.391384-12

2011

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Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum

Molecular and cellular neuroscience, 2007-05, Vol.35 (1), p.161-170

2007

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Genetic Analysis of a New Mouse Model for Non-Insulin-Dependent Diabetes

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.273-286

2001

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A new mouse model of metabolic syndrome and associated complications

Journal of endocrinology, 2009-07, Vol.202 (1), p.17-28

2009

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Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ

Investigative ophthalmology & visual science, 2016-03, Vol.57 (3), p.877-888

2016

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Microtubule-associated protein 1A is a modifier of tubby hearing ( moth1 )

Nature genetics, 2002-04, Vol.30 (4), p.401-405

2002

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Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele

Investigative ophthalmology & visual science, 2018-10, Vol.59 (12), p.5127-5139

2018

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Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosa

Human molecular genetics, 2013-02, Vol.22 (3), p.558-567

2013

Volltextzugriff (PDF)

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1 rd8 mouse model

PLoS genetics, 2022-06, Vol.18 (6), p.e1009798

2022

Volltextzugriff (PDF)

Bright-Field Imaging and Optical Coherence Tomography of the Mouse Posterior Eye

Methods in molecular biology (Clifton, N.J.), 2016-01, Vol.1438, p.395

2016

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Defective carbohydrate metabolism in mice homozygous for the tubby mutation

Physiological genomics, 2006-10, Vol.27 (2), p.131-140

2006

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CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina

Human molecular genetics, 2003-09, Vol.12 (17), p.2179-2189

2003

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Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction

Experimental eye research, 2009-09, Vol.89 (3), p.365-372

2009

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A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia

Investigative ophthalmology & visual science, 2015-06, Vol.56 (6), p.3776-3787

2015

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Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis

Investigative ophthalmology & visual science, 2012-02, Vol.53 (2), p.967-974

2012

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A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density

Molecular vision, 2017-03, Vol.23, p.140-148

2017

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A Novel Dwarfism with Gonadal Dysfunction Due to Loss-of-Function Allele of the Collagen Receptor Gene, Ddr2, in the Mouse

Molecular endocrinology (Baltimore, Md.), 2008-08, Vol.22 (8), p.1866-1880

2008

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Deficiency in Lyst function leads to accumulation of secreted proteases and reduced retinal adhesion

Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model

Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes

NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Degradation of IRS1 leads to impaired glucose uptake in adipose tissue of the type 2 diabetes mouse model TALLYHO/Jng

Epithelial mechanics are maintained by inhibiting cell fusion with age in Drosophila

Mouse Model Resources for Vision Research

Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum

Genetic Analysis of a New Mouse Model for Non-Insulin-Dependent Diabetes

A new mouse model of metabolic syndrome and associated complications

Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ

Microtubule-associated protein 1A is a modifier of tubby hearing ( moth1 )

Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele

Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosa

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1 rd8 mouse model

Bright-Field Imaging and Optical Coherence Tomography of the Mouse Posterior Eye

Defective carbohydrate metabolism in mice homozygous for the tubby mutation

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina

Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction

A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia

Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis

A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density

A Novel Dwarfism with Gonadal Dysfunction Due to Loss-of-Function Allele of the Collagen Receptor Gene, Ddr2, in the Mouse

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