(Q44535894)

3 December 2017

title

Studies on the metabolic fate of n-3 polyunsaturated fatty acids (English)

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(4Z,7Z,10Z,13Z,16Z,19Z)-docosahexaenoyl-CoA

3 December 2017

0 references

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ChEBI release 2020-05-28

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ChEBI release 2020-05-28

4

Ronald J A Wanders

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3 December 2017

1

Sacha Ferdinandusse

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3 December 2017

Simone Denis

2

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3 December 2017

Georges Dacremont

series ordinal

3

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3 December 2017

publication date

1 August 2003

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Journal of Lipid Research

3 December 2017

published in

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3 December 2017

volume

44

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3 December 2017

issue

10

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3 December 2017

page(s)

1992-1997

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The biochemistry of n-3 polyunsaturated fatty acids

3 December 2017

cites work

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https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Polyunsaturated fatty acid biosynthesis: a microsomal-peroxisomal process

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Comparison of the binding affinities of acyl-CoA-binding protein and fatty-acid-binding protein for long-chain acyl-CoA esters

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Fatty acid oxidation disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Disorders of mitochondrial fatty acyl-CoA beta-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Peroxisomal beta-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

L-2-hydroxyglutarate dehydrogenase: identification of a novel enzyme activity in rat and human liver. Implications for L-2-hydroxyglutaric acidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Metabolism of highly unsaturated n-3 and n-6 fatty acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

Characterisation of human peroxisomal 2,4-dienoyl-CoA reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

The mouse gene PDCR encodes a peroxisomal delta(2), delta(4)-dienoyl-CoA reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.M300223-JLR200

10.1194/JLR.M300223-JLR200

21 January 2018

Identifiers

DOI

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3 December 2017

1 reference