A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration (Q34829498)

4 August 2017

title

A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration (English)

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4 August 2017

1 reference

Venkata R M Chavali

1

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4 August 2017

Naheed W Khan

2

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4 August 2017

Catherine A Cukras

3

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4 August 2017

Dirk-Uwe Bartsch

4

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4 August 2017

Monica M Jablonski

5

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4 August 2017

Radha Ayyagari

6

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4 August 2017

publication date

24 February 2011

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4 August 2017

published in

Human Molecular Genetics

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4 August 2017

volume

20

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4 August 2017

issue

10

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4 August 2017

page(s)

2000-2014

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Virtual microscopy, data management and image analysis in Aperio ScanScope system

4 August 2017

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Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

8 July 2018

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Oxidative stress-induced mitochondrial DNA damage in human retinal pigment epithelial cells: a possible mechanism for RPE aging and age-related macular degeneration

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Phenotypic marker for early disease detection in dominant late-onset retinal degeneration.

26 October 2018

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26 October 2018

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26 October 2018

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The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in mice

26 October 2018

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Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration

21 January 2018

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21 January 2018

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9 December 2018

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The topography and age relationship of lipofuscin concentration in the retinal pigment epithelium

9 December 2018

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12 December 2020

Lipofuscin of human retinal pigment epithelium

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Extensive subretinal pigment epithelial deposit in two brothers suffering from dominant retinitis pigmentosa. A histopathological study

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Abnormal dark adaptation and rhodopsin kinetics in Sorsby's fundus dystrophy

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Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene

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Photodamage to human RPE cells by A2-E, a retinoid component of lipofuscin

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Diffuse cellular and fibrosing interstitial pneumonitis with desquamative interstitial pneumonitis-like features associated with myeloid neoplasia

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The spatio-temporal pattern of photoreceptor degeneration in the aged rd/rd mouse retina

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Morphologic changes in age-related maculopathy

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12 December 2020

Fundus autofluorescence in age-related macular disease imaged with a laser scanning ophthalmoscope

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12 December 2020

Identifiers

DOI

10.1093/HMG/DDR080

1 reference

4 August 2017

1 reference

4 August 2017

1 reference