Results 141 to 150 of about 2,517,871 (188)

Utilising phytanic acid diastereomers for the characterisation of archaeological lipid residues in pottery samples [PDF]

open access: yesTetrahedron Letters, 2016
Phytanic acid diastereomers, 3S,7R,11R,15-phytanic acid (SRR) and 3R,7R,11R,15-phytanic acid (RRR), were determined by GC-MS in extracts of archaeological ceramic.
Andre Carlo Colonese   +2 more
exaly   +3 more sources

Phytanic acid: production from phytol, its breakdown and role in human disease

open access: yesCellular and Molecular Life Sciences, 2006
Phytanic acid is a branched-chain fatty acid that accumulates in a variety of metabolic disorders. High levels of phytanic acid found in patients can exceed the millimolar range and lead to severe symptoms.
Ronald Wanders, Daan M Van Den Brink
exaly   +2 more sources

Intraorganellar localization of CoASH-independent phytanic acid oxidation in human liver peroxisomes [PDF]

open access: yesFEBS Letters, 1993
In human tissues phytanic acid is α-oxidized to pristanic acid in peroxisomes. Studies of the intraorganellar site of α-oxidation of [1-14C]phytanic acid to pristanic acid in peroxisomes isolated from human liver demonstrate that phytanoyl-CoA ligase is ...
Kalipada Pahan, Inderjit Singh
exaly   +2 more sources

Human metabolism of phytanic acid and pristanic acid

Progress in Lipid Research, 2001
Phytanic acid is a methyl-branched fatty acid present in the human diet. Due to its structure, degradation by beta-oxidation is impossible. Instead, phytanic acid is oxidized by alpha-oxidation, yielding pristanic acid. Despite many efforts to elucidate the alpha-oxidation pathway, it remained unknown for more than 30 years.
N M, Verhoeven, C, Jakobs
openaire   +2 more sources

Neurological disorders and phytanic acid metabolism

Acta Neurologica Scandinavica, 1988
Fifty patients with neurological symptoms and signs resembling those of Refsum's disease were analyzed for phytanic acid in serum. In addition, the phytanic acid oxidase capacity in skin fibroblasts was determined. The patients suffered from retinitis pigmentosa, cerebellar ataxia and/or chronic polyneuropathy of unknown cause.
O H, Skjeldal   +2 more
openaire   +2 more sources

Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndrome

open access: yesClinica Chimica Acta, 1987
Plasma samples from several Zellweger patients were found to contain elevated phytanic acid levels. It was subsequently found that the level of phytanic acid in plasma from Zellweger patients depends upon the age of the patients at the time of sampling ...
P G Barth, R B H Schutgens, P G Barth
exaly   +2 more sources

METABOLISM OF PHYTANIC ACID IN REFSUM'S DISEASE

The Lancet, 1982
Abstract Because patients with Refsum's disease lack an α-hydroxylase they are unable to metabolise phytanic acid, which is present in most foods. However, a study of urinary metabolites in 4 patients with Refsum's disease demonstrated that ω-oxidation can replace the normal oxidation process to some extent.
J D, Billimoria   +3 more
openaire   +2 more sources

Transport of Phytanic Acid on Lipoproteins in Refsum's Disease

Clinical Science, 1998
AbstractPatients with Refsum disease accumulate significant quantities of phytanic acid in adipose and neural tissue. The accumulation can be reversed by following a diet low in phytanic acid, yet the mechanism of transport of this fatty acid is obscure.
A S, Wierzbicki   +5 more
openaire   +2 more sources

The stereochemistry of phytanic acid in Refsum's Syndrome

Lipids, 1970
AbstractPhytanic acid has been isolated from the total lipids of the liver of a human suffering from the disease, Refsum's Syndrome (Heredopathia atactica polyneuritiformis). Optical rotation measurements were made on the acid, and on the ketone 6,10,14‐trimethylpentadecan‐2‐one which resulted from the oxidative degradation of the acid and the ...
openaire   +2 more sources

Phytanic Acid, Amacr and Prostate Cancer Risk

Future Oncology, 2006
The growing body of knowledge in cancer prevention demonstrates that for many cancers, risk must be defined in terms of both environmental and genetic factors. In prostate cancer, there is increasing evidence linking risk with polymorphisms in the alpha-methylacyl-CoA racemase (AMACR) gene and branched-chain fatty acids derived from specific sources of
Todd, Thornburg   +5 more
openaire   +2 more sources

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