(Q34099124)

31 July 2017

Biochemical defects in 11-cis-retinol dehydrogenase mutants associated with fundus albipunctatus (English)

1 reference

31 July 2017

Retinol dehydrogenase 5

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protein homodimerization activity

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Lidén M

1

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31 July 2017

Romert A

2

1 reference

31 July 2017

Tryggvason K

3

1 reference

31 July 2017

Persson B

4

1 reference

31 July 2017

Eriksson U

5

1 reference

31 July 2017

language of work or name

English

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publication date

23 October 2001

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Journal of Biological Chemistry

31 July 2017

7

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based on heuristic

inferred from page(s)

published in

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31 July 2017

276

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31 July 2017

49251-49257

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31 July 2017

52

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Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.

31 July 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

A novel compound heterozygous mutation in the RDH5 gene in a patient with fundus albipunctatus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus11The authors have no proprietary interest in any of the materials used in this study

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Identification and characterization of a stereospecific human enzyme that catalyzes 9-cis-retinol oxidation. A possible role in 9-cis-retinoic acid formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

The identification of a 9-cis retinol dehydrogenase in the mouse embryo reveals a pathway for synthesis of 9-cis retinoic acid.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Activity of human 11-cis-retinol dehydrogenase (Rdh5) with steroids and retinoids and expression of its mRNA in extra-ocular human tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Primary structure of human 11-cis retinol dehydrogenase and organization and chromosomal localization of the corresponding gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Production of single-stranded plasmid DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Rapid and efficient site-specific mutagenesis without phenotypic selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Gene structure, expression analysis, and membrane topology of RDH4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Biosynthesis of 9-cis-retinoic acid in vivo. The roles of different retinol dehydrogenases and a structure-activity analysis of microsomal retinol dehydrogenases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

A novel pathway for vitamin A signaling mediated by RXR heterodimerization with NGFI-B and NURR1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Structure of human estrogenic 17 beta-hydroxysteroid dehydrogenase at 2.20 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

KIND-a non-redundant protein database.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Improved tools for biological sequence comparison

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M107337200

21 January 2018

Identifiers

DOI

10.1074/JBC.M107337200

1 reference

31 July 2017

1 reference