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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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Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss

Cells (Basel, Switzerland), 2020-04, Vol.9 (4), p.931

2020

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Mutations in Lama1 Disrupt Retinal Vascular Development and Inner Limiting Membrane Formation

The Journal of biological chemistry, 2010-03, Vol.285 (10), p.7697-7711

2010

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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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Prefoldin 5 Is Required for Normal Sensory and Neuronal Development in a Murine Model

The Journal of biological chemistry, 2011-01, Vol.286 (1), p.726-736

2011

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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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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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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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Current Views on Chr10q26 Contribution to Age-Related Macular Degeneration

Advances in experimental medicine and biology, 2023, Vol.1415, p.27-36

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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Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments

Visual neuroscience, 2008-07, Vol.25 (4), p.563-574

2008

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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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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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Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation

Human molecular genetics, 2015-12, Vol.24 (24), p.6958-6974

2015

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An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency

Human molecular genetics, 2018-10, Vol.27 (19), p.3340-3352

2018

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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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Mouse Models of NMNAT1 -Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease

The American journal of pathology, 2016-07, Vol.186 (7), p.1925-1938

2016

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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

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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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Lysosomal Trafficking Regulator (LYST)

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

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

Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss

Mutations in Lama1 Disrupt Retinal Vascular Development and Inner Limiting Membrane Formation

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Prefoldin 5 Is Required for Normal Sensory and Neuronal Development in a Murine Model

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

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

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

Current Views on Chr10q26 Contribution to Age-Related Macular Degeneration

Mouse Model Resources for Vision Research

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

Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments

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

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

A new mouse model of metabolic syndrome and associated complications

Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation

An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency

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

Mouse Models of NMNAT1 -Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease

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

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

Lysosomal Trafficking Regulator (LYST)

Defective carbohydrate metabolism in mice homozygous for the tubby mutation

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

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

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