(Q47852289)

6 February 2018

title

Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acid (English)

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6 February 2018

author name string

Verhoeven NM

1

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6 February 2018

Jakobs C

2

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6 February 2018

Carney G

3

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6 February 2018

Somers MP

4

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6 February 2018

Wanders RJ

5

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6 February 2018

Rizzo WB

6

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6 February 2018

language of work or name

English

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publication date

1 June 1998

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6 February 2018

number of pages

4

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based on heuristic

inferred from page(s)

published in

FEBS Letters

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6 February 2018

volume

429

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6 February 2018

issue

3

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6 February 2018

page(s)

225-228

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6 February 2018

Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Production of formyl-CoA during peroxisomal alpha-oxidation of 3-methyl-branched fatty acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Identification of PAHX, a Refsum disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Human liver fatty aldehyde dehydrogenase: microsomal localization, purification, and biochemical characterization

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Sjögren-Larsson syndrome. Deficient activity of the fatty aldehyde dehydrogenase component of fatty alcohol:NAD+ oxidoreductase in cultured fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Sjögren-Larsson syndrome. Impaired fatty alcohol oxidation in cultured fibroblasts due to deficient fatty alcohol:nicotinamide adenine dinucleotide oxidoreductase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Isolation of animal cell mutants defective in long-chain fatty aldehyde dehydrogenase. Sensitivity to fatty aldehydes and Schiff's base modification of phospholipids: implications for Sj-ogren-Larsson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Phospholipid fatty acid composition in type I and type II rat muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Formation of a 2-methyl-branched fatty aldehyde during peroxisomal α-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Phytanic acid alpha-oxidation in rat liver peroxisomes. Production of alpha-hydroxyphytanoyl-CoA and formate is enhanced by dioxygenase cofactors

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

alpha-Oxidation of 3-methyl-substituted fatty acids in rat liver. Production of formic acid instead of CO2, cofactor requirements, subcellular localization and formation of a 2-hydroxy-3-methylacyl-CoA intermediate

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Resolution of the phytanic acid alpha-oxidation pathway: identification of pristanal as product of the decarboxylation of 2-hydroxyphytanoyl-CoA

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Phytanoyl-coenzyme A hydroxylase deficiency -- the enzyme defect in Refsum's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

Phytanic acid alpha-oxidation in peroxisomal disorders: studies in cultured human fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900574-2

10.1016/S0014-5793(98)00574-2

21 January 2018

Identifiers

DOI

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6 February 2018

1 reference

6 February 2018