Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome.
The cerebro-hepato-renal (Zellweger) syndrome is an autosomal recessive disorder biochemically characterized by the absence of morphologically distinguishable peroxisomes. Key enzymes involved in the biosynthesis of ether phospholipids, i.e., dihydroxyacetone phosphate acyltransferase and alkyl dihy...
Main Authors: | G Schrakamp, C F Roosenboom, R B Schutgens, R J Wanders, H S Heymans, J M Tager, H van den Bosch |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
1985-07-01
|
Series: | Journal of Lipid Research |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520343170 |
Similar Items
-
Exclusive localization in peroxisomes of dihydroxyacetone phosphate acyltransferase and alkyl-dihydroxyacetone phosphate synthase in rat liver.
by: H Singh, et al.
Published: (1993-03-01) -
Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.
by: G Schrakamp, et al.
Published: (1988-03-01) -
Prenatal Diagnosis of Zellweger Syndrome: Case Report
by: Bilgin Kütükcü, et al.
Published: (2016-05-01) -
The effect of high sugar intake on the esterification of dihydroxyacetone phosphate by rat liver microsomes
by: R G Lamb, et al.
Published: (1976-07-01) -
Lipidomic analysis of fibroblasts from Zellweger spectrum disorder patients identifies disease-specific phospholipid ratios[S]
by: Katharina Herzog, et al.
Published: (2016-08-01)