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Phytanic Acid
Known as:
Hexadecanoic acid, 3,7,11,15-tetramethyl-
, Acid, Phytanic
, acid phytanic
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A 20-carbon branched chain fatty acid. In phytanic acid storage disease (REFSUM DISEASE) this lipid may comprise as much as 30% of the total fatty…
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National Institutes of Health
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Related topics
Related topics
12 relations
Narrower (5)
2-hydroxyphytanic acid
2-oxophytanic acid
Phytanate
phytanoyl-coenzyme A
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In Blood
agonists
analogs & derivatives
antagonists & inhibitors
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2001
2001
Identification of pristanal dehydrogenase activity in peroxisomes: conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomes.
G. Jansen
,
M. BrinkvandenD.
,
R. Ofman
,
O. Drăghici
,
G. Dacrement
,
R. J. Wanders
Biochemical and Biophysical Research…
2001
Corpus ID: 42558720
Phytanic acid (3,7,11,15-tetramethylhexadecanoic acid) is a branched-chain fatty acid which, due to the methyl-group at the 3…
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1994
1994
2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndrome.
R. J. Wanders
,
C. V. van Roermund
,
D. S. Schor
,
H. T. Ten Brink
,
C. Jakobs
Biochimica et Biophysica Acta
1994
Corpus ID: 30640553
Highly Cited
1985
Highly Cited
1985
Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: Plasma changes and skin fibroblast phytanic acid oxidase
A. Poulos
,
P. Sharp
,
A. Fellenberg
,
D. Danks
Human Genetics
1985
Corpus ID: 6816592
SummaryCerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease patients can be divided into at…
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Highly Cited
1984
Highly Cited
1984
Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?
A. Poulos
,
P. Sharp
,
M. Whiting
Clinical Genetics
1984
Corpus ID: 38821991
The activity of phytanic acid oxidase is low in infantile and adult Refsum's disease, and in the cerebro‐hepato‐renal (Zellweger…
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Highly Cited
1984
Highly Cited
1984
Patterns of Refsum's disease. Phytanic acid oxidase deficiency.
A. Poulos
,
A. Pollard
,
J. Mitchell
,
G. Wise
,
G. Mortimer
Archives of Disease in Childhood
1984
Corpus ID: 12920001
Four children each exhibiting a profound deficiency of phytanic acid oxidase activity in cultured skin fibroblasts but with very…
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1983
1983
Phytanic acid storage disease
G. Djupesland
,
G. Flottorp
,
S. Refsum
Neurology
1983
Corpus ID: 21178003
Heredopathia atactica polyneuritiformis is a biochemically defined disease with a specific dietary treatment. It is an autosomal…
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Highly Cited
1969
Highly Cited
1969
Refsum's disease: defective oxidation of phytanic acid in tissue cultures derived from homozygotes and heterozygotes.
J. Herndon
,
D. Steinberg
,
B. Uhlendorf
New England Journal of Medicine
1969
Corpus ID: 11827018
Abstract A defect in phytanic acid oxidation was demonstrated in cultured fibroblasts derived from skin biopsies of 11 patients…
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Highly Cited
1967
Highly Cited
1967
A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. I. Clinical, pathologic and biochemical characteristics.
G. Shy
,
D. Silberberg
,
S. Appel
,
M. Mishkin
,
E. Godfrey
American Journal of Medicine
1967
Corpus ID: 34728383
Highly Cited
1966
Highly Cited
1966
Phytol metabolism in the bovine.
Stuart Patton
,
Stuart Patton
,
Andrew A. Benson
,
Andrew A. Benson
Biochimica et Biophysica Acta
1966
Corpus ID: 45863928
1964
1964
Blood lipids. 4. The isolation of 3,7,11,15-tetramethylhexadecanoic acid (phytanic acid) from ox-plasma lipids.
A. Lough
Biochemical Journal
1964
Corpus ID: 45524674
The presence of an unusual peak on gas-liquid chromatograms of methyl esters of fatty acids derived from lipids
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