Targeted disruption of the murine retinal dehydrogenase gene Rdh12 does not limit visual cycle function (Q35641844)

9 August 2017

title

Targeted disruption of the murine retinal dehydrogenase gene Rdh12 does not limit visual cycle function (English)

1 reference

9 August 2017

Ingo Kurth

1

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Christian A. Hübner

11

object named as

Christian A Hübner

1 reference

9 August 2017

Debra A Thompson

2

1 reference

9 August 2017

Klaus Rüther

3

1 reference

9 August 2017

Kecia L Feathers

4

1 reference

9 August 2017

Jared D Chrispell

5

1 reference

9 August 2017

Jana Schroth

6

1 reference

9 August 2017

Christina L McHenry

7

1 reference

9 August 2017

Michaela Schweizer

8

1 reference

9 August 2017

Sergej Skosyrski

9

1 reference

9 August 2017

Andreas Gal

10

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9 August 2017

language of work or name

English

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publication date

27 November 2006

1 reference

Molecular and Cellular Biology

9 August 2017

published in

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9 August 2017

volume

27

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9 August 2017

issue

4

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9 August 2017

page(s)

1370-1379

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Mouse phenogenomics: the fast track to "systems metabolism".

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle

27 July 2018

1 reference

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Opsin activation of transduction in the rods of dark-reared Rpe65 knockout mice

27 July 2018

1 reference

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27 July 2018

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Downregulation of cone-specific gene expression and degeneration of cone photoreceptors in the Rpe65-/- mouse at early ages

27 July 2018

1 reference

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Functional characterization of mouse RDH11 as a retinol dehydrogenase involved in dark adaptation in vivo

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Delayed dark adaptation in 11-cis-retinol dehydrogenase-deficient mice: a role of RDH11 in visual processes in vivo

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis

27 July 2018

1 reference

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Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

27 July 2018

1 reference

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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

27 July 2018

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Cloning and characterization of a novel all-trans retinol short-chain dehydrogenase/reductase from the RPE

27 July 2018

1 reference

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Dual-substrate specificity short chain retinol dehydrogenases from the vertebrate retina

27 July 2018

1 reference

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Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.

27 July 2018

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Stereoisomeric specificity of the retinoid cycle in the vertebrate retina

27 July 2018

1 reference

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Disruption of the 11-cis-retinol dehydrogenase gene leads to accumulation of cis-retinols and cis-retinyl esters

27 July 2018

1 reference

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A QTL on distal chromosome 3 that influences the severity of light-induced damage to mouse photoreceptors

27 July 2018

1 reference

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Phase partition and high-performance liquid chromatography assays of retinoid dehydrogenases

27 July 2018

1 reference

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Identification and characterization of all-trans-retinol dehydrogenase from photoreceptor outer segments, the visual cycle enzyme that reduces all-trans-retinal to all-trans-retinol

27 July 2018

1 reference

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Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus

27 July 2018

1 reference

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Molecular characterization of a novel short-chain dehydrogenase/reductase that reduces all-trans-retinal

27 July 2018

1 reference

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Reduced stress defense in heme oxygenase 1-deficient cells.

27 July 2018

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Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Retinoschisislike alterations in the mouse eye caused by gene targeting of the Norrie disease gene.

27 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

The retinal pigment epithelial-specific 11-cis retinol dehydrogenase belongs to the family of short chain alcohol dehydrogenases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Cone opsin mislocalization in Rpe65-/- mice: a defect that can be corrected by 11-cis retinal

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

A photic visual cycle of rhodopsin regeneration is dependent on Rgr.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

The Rpe65 Leu450Met variation increases retinal resistance against light-induced degeneration by slowing rhodopsin regeneration.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

A reliable procedure for comparison of antioxidants in rat brain homogenates

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Mutations in RPE65 cause Leber's congenital amaurosis

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800705

Slowly progressive changes of the retina and retinal pigment epithelium in Briard dogs with hereditary retinal dystrophy. A morphological study

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17130236

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1128/MCB.01486-06

1 reference

9 August 2017

1 reference

9 August 2017

1 reference