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dihydroxyacetone phosphate and Peroxisomal Disorders

dihydroxyacetone phosphate has been researched along with Peroxisomal Disorders in 2 studies

Dihydroxyacetone Phosphate: An important intermediate in lipid biosynthesis and in glycolysis.
dihydroxyacetone phosphate : A member of the class of glycerone phosphates that consists of glycerone bearing a single phospho substituent.

Peroxisomal Disorders: A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hajra, AK2
Das, AK1

Reviews

2 reviews available for dihydroxyacetone phosphate and Peroxisomal Disorders

ArticleYear
Glycerolipid biosynthesis in peroxisomes (microbodies).
    Progress in lipid research, 1995, Volume: 34, Issue:4

    Topics: Animals; Dihydroxyacetone Phosphate; Humans; Lipids; Microbodies; Peroxisomal Disorders; Signal Tran

1995
Lipid biosynthesis in peroxisomes.
    Annals of the New York Academy of Sciences, 1996, Dec-27, Volume: 804

    Topics: Acyltransferases; Aldehyde Oxidoreductases; Animals; Cell Compartmentation; Dihydroxyacetone Phospha

1996