(Q28269121)

1

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S J Mihalik

2

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P A Watkins

3

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C Jakobs

4

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H W Moser

5

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R J Wanders

Phytanic acid must be activated to phytanoyl-CoA prior to its alpha-oxidation in rat liver peroxisomes

6

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language of work or name

English

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publication date

23 March 1998

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published in

Clinica Chimica Acta

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volume

271

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issue

2

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page(s)

203-11

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

Measurement of protein using bicinchoninic acid

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

The role of ascorbate in the prolyl hydroxylase reaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

Role of iron, hydrogen peroxide and reactive oxygen species in microsomal oxidation of glycerol to formaldehyde

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

Ketoconazole and other imidazole derivatives are potent inhibitors of peroxisomal phytanic acid alpha-oxidation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

7 January 2021

Peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3

7 January 2021

PEX genes on the rise

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900259-3