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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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Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations

Annual review of neuroscience, 2003-01, Vol.26, p.657-700

2003

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Mouse Model Resources for Vision Research

Journal of ophthalmology, 2011-01, Vol.2011 (2011), p.1-12

2011

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The Impact of Adherens and Tight Junctions on Physiological Function and Pathological Changes in the Retina

Advances in experimental medicine and biology, 2018, Vol.1074, p.545-551

2018

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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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Lysosomal Trafficking Regulator (LYST)

Advances in experimental medicine and biology, 2016-01, Vol.854, p.745-750

2016

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New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene

Human molecular genetics, 2009-01, Vol.18 (1), p.178-192

2009

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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 Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects

Advances in experimental medicine and biology, 2016-01, Vol.854, p.177-183

2016

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Myosin 6 is required for iris development and normal function of the outer retina

Investigative ophthalmology & visual science, 2013-11, Vol.54 (12), p.7223-7233

2013

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An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant Mice

Investigative ophthalmology & visual science, 2012-03, Vol.53 (3), p.1663-1669

2012

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An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration

Investigative ophthalmology & visual science, 2011-06, Vol.52 (7), p.4703-4709

2011

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Genetic modifier loci of mouse Mfrp(rd6) identified by quantitative trait locus analysis

Experimental eye research, 2014-01, Vol.118, p.30-35

2014

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Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6

Human molecular genetics, 2002-08, Vol.11 (16), p.1879-1886

2002

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Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2

Investigative ophthalmology & visual science, 2010-06, Vol.51 (6), p.3264-3272

2010

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Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with Retinitis pigmentosa

Nature genetics, 1998-02, Vol.18 (2), p.174-176

1998

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Translational vision research models program

Advances in experimental medicine and biology, 2012, Vol.723, p.391

2012

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Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene

Human molecular genetics, 2000-01, Vol.9 (2), p.155-163

2000

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Cell-Specific Expression of Tubby Gene Family Members (tub, Tulp1, 2, and 3) in the Retina

Investigative ophthalmology & visual science, 1999-10, Vol.40 (11), p.2706-2712

1999

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Severe Ocular Abnormalities in C57BL/6 but Not in 129/Sv p53-Deficient Mice

Investigative ophthalmology & visual science, 1999-07, Vol.40 (8), p.1874-1878

1999

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Genetic Modification of Retinal Degeneration in Tubby Mice

Experimental eye research, 2002-04, Vol.74 (4), p.455-461

2002

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From Vivarium to Bedside: Lessons Learned from Animal Models

Ophthalmic genetics, 2006-12, Vol.27 (4), p.123-137

2006

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

Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations

Mouse Model Resources for Vision Research

The Impact of Adherens and Tight Junctions on Physiological Function and Pathological Changes in the Retina

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

Lysosomal Trafficking Regulator (LYST)

New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene

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 Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects

Myosin 6 is required for iris development and normal function of the outer retina

An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant Mice

An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration

Genetic modifier loci of mouse Mfrp(rd6) identified by quantitative trait locus analysis

Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6

Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with Retinitis pigmentosa

Translational vision research models program

Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene

Cell-Specific Expression of Tubby Gene Family Members (tub, Tulp1, 2, and 3) in the Retina

Severe Ocular Abnormalities in C57BL/6 but Not in 129/Sv p53-Deficient Mice

Genetic Modification of Retinal Degeneration in Tubby Mice

From Vivarium to Bedside: Lessons Learned from Animal Models

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