Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren-Larsson syndrome (Q28631733)

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6 November 2019

title

Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren-Larsson syndrome (English)

2 references

3 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11306053%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

W B Rizzo

series ordinal

1

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6 November 2019

Z Lin

series ordinal

2

1 reference

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6 November 2019

G Carney

series ordinal

3

1 reference

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6 November 2019

publication date

1 January 2001

1 reference

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Chemico-biological Interactions

6 November 2019

published in

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3 February 2017

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6 November 2019

volume

130-132

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3 February 2017

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6 November 2019

issue

1-3

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3 February 2017

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6 November 2019

page(s)

297-307

1 reference

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6 November 2019

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Microsomal aldehyde dehydrogenase or its cross-reacting protein exists in outer mitochondrial membranes and peroxisomal membranes in rat liver

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Defective inactivation of leukotriene B4 in patients with Sjögren-Larsson syndrome

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Mouse microsomal Class 3 aldehyde dehydrogenase: AHD3 cDNA sequence, inducibility by dioxin and clofibrate, and genetic mapping

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Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene

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Microsomal aldehyde dehydrogenase is localized to the endoplasmic reticulum via its carboxyl-terminal 35 amino acids

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Relationships within the aldehyde dehydrogenase extended family

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The first structure of an aldehyde dehydrogenase reveals novel interactions between NAD and the Rossmann fold

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Genomic organization and expression of the human fatty aldehyde dehydrogenase gene (FALDH)

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Human fatty aldehyde dehydrogenase gene (ALDH10): organization and tissue-dependent expression

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Genomic organization, expression, and alternate splicing of the mouse fatty aldehyde dehydrogenase gene

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Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement

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Sjögren-Larsson syndrome is caused by a common mutation in northern European and Swedish patients

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A common deletion mutation in European patients with Sjögren-Larsson syndrome.

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A missense mutation in the FALDH gene identified in Sjögren-Larsson syndrome patients originating from the northern part of Sweden.

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Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome

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A novel 4 bp deletion mutation in the FALDH gene segregating in a Turkish family with Sjögren-Larsson syndrome

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The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene

7 January 2021

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Molecular basis of Sjögren-Larsson syndrome: frequency of the 1297-1298 del GA and 943C-->T mutation in 29 patients

7 January 2021

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A novel point mutation of the FALDH gene in a Japanese family with Sjögren-Larsson syndrome

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7 January 2021

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Some properties of the fatty alcohol oxidation system and reconstitution of microsomal oxidation activity in intestinal mucosa

7 January 2021

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Microsomal fatty aldehyde dehydrogenase catalyzes the oxidation of aliphatic aldehyde derived from ether glycerolipid catabolism: implications for Sjögren-Larsson syndrome

7 January 2021

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10.1016/S0009-2797(00)00273-8

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11306053%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

2 references

3 February 2017