(Q28609399)

3 February 2017

title

Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomes (English)

1 reference

3 February 2017

J. Biermann

1

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3 February 2017

W. W. Just

series ordinal

2

1 reference

3 February 2017

R. J. Wanders

series ordinal

3

1 reference

3 February 2017

H. Van Den Bosch

series ordinal

4

1 reference

3 February 2017

language of work or name

English

0 references

publication date

1 April 1999

1 reference

3 February 2017

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3 February 2017

volume

261

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3 February 2017

issue

2

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3 February 2017

page(s)

492–499

1 reference

Ether lipid biosynthesis: isolation and molecular characterization of human dihydroxyacetonephosphate acyltransferase

3 February 2017

cites work

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00295.X

Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00295.X

Alkyl-dihydroxyacetonephosphate synthase. Fate in peroxisome biogenesis disorders and identification of the point mutation underlying a single enzyme deficiency

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00295.X

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 April 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Acyl dihydroxyacetone phosphate: Precursor of alkyl ethers

21 April 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Immunological localization and tissue distribution of alkyldihydroxyacetonephosphate synthase and deficiency of the enzyme in peroxisomal disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Rat liver dihydroxyacetone-phosphate acyltransferase: enzyme characteristics and localization studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Biochemistry of peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Differential deficiency of mevalonate kinase and phosphomevalonate kinase in patients with distinct defects in peroxisome biogenesis: evidence for a major role of peroxisomes in cholesterol biosynthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

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/10.1046%2FJ.1432-1327.1999.00295.X

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/10.1046%2FJ.1432-1327.1999.00295.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Nucleotide sequence of human alkyl-dihydroxyacetonephosphate synthase cDNA reveals the presence of a peroxisomal targeting signal 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Polymerase chain reaction-based cloning of alkyl-dihydroxyacetonephosphate synthase complementary DNA from guinea pig liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Identification of PAHX, a Refsum disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Differential protein import deficiencies in human peroxisome assembly disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

The native molecular size of alkyl-dihydroxyacetonephosphate synthase and dihydroxyacetonephosphate acyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1327.1999.00295.X

10.1046/J.1432-1327.1999.00295.X

21 January 2018

Identifiers

DOI

0 references

1 reference