(Q55035898)

16 June 2018

title

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

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16 June 2018

3

Ronald J A Wanders

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16 June 2018

Sacha Ferdinandusse

series ordinal

1

object named as

Sacha Ferdinandusse

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16 June 2018

author name string

Thomas Meissner

series ordinal

2

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16 June 2018

Ertan Mayatepek

series ordinal

4

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16 June 2018

language of work or name

English

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publication date

1 April 2002

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16 June 2018

Biochemical and Biophysical Research Communications

published in

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16 June 2018

volume

293

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16 June 2018

issue

1

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16 June 2018

page(s)

269-273

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16 June 2018

Leukotrienes: biosynthesis, metabolism, and pathophysiologic significance

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

Prostaglandins and leukotrienes: advances in eicosanoid biology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

Impaired degradation of leukotrienes in patients with peroxisome deficiency disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

Defective degradation of leukotrienes in peroxisomal-deficient human hepatocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

Increased urinary excretion of LTB4 and omega-carboxy-LTB4 in patients with Zellweger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

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%2FS0006-291X%2802%2900214-0

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%2FS0006-291X%2802%2900214-0

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%2FS0006-291X%2802%2900214-0

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

Leukotriene C4 synthesis deficiency: a member of a probably underdiagnosed new group of neurometabolic diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions of the fatty acid alpha- and beta-oxidation systems in humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900214-0

10.1016/S0006-291X(02)00214-0

7 January 2021

Identifiers

DOI

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16 June 2018

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16 June 2018