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Journal of Lipid Research
|
July 1, 1993
Peroxisomal chain-shortening of thromboxane B2: evidence for impaired degradation of thromboxane B2 in Zellweger syndrome
U Diczfalusy, O Vesterqvist, B F Kase, et al.
Biochimica Et Biophysica Acta
|
March 14, 1989
Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts
E Christensen, M Grønn, T A Hagve, et al.
Journal of the Neurological Sciences
|
May 1, 1988
Infantile Refsum's disease: a generalized peroxisomal disorder. Case report with postmortem examination
A Torvik, S Torp, B F Kase, et al.
Pediatric Research
|
January 1, 1991
Importance of peroxisomes in the formation of chenodeoxycholic acid in human liver. Metabolism of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid in Zellweger syndrome
B F Kase, J I Pedersen, K O Wathne, et al.
The Biochemical Journal
|
October 21, 1999
Sulphation of lithocholic acid in the colon-carcinoma cell line CaCo-2
B Halvorsen, B F Kase, K Prydz, et al.
Human Genetics
|
February 1, 1996
Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndrome
T C Olsen, H G Eiken, P M Knappskog, et al.
Biochimica Et Biophysica Acta
|
August 15, 1984
Urinary excretion of dicarboxylic acids from patients with the Zellweger syndrome. Importance of peroxisomes in beta-oxidation of dicarboxylic acids
I Björkhem, S Blomstrand, P Hågå, et al.
Clinical Chemistry
|
August 21, 2004
Screening for serum total homocysteine in newborn children
Helga Refsum, Anne W Grindflek, Per M Ueland, et al.
Clinical Chemistry
|
August 6, 2000
Evaluation of novel assays in clinical chemistry: quantification of plasma total homocysteine
E Nexo, F Engbaek, P M Ueland, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 69) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 69 results.
Journal of Lipid Research
|
July 1, 1993
Peroxisomal chain-shortening of thromboxane B2: evidence for impaired degradation of thromboxane B2 in Zellweger syndrome
U Diczfalusy, O Vesterqvist, B F Kase, et al.
Biochimica Et Biophysica Acta
|
March 14, 1989
Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts
E Christensen, M Grønn, T A Hagve, et al.
Journal of the Neurological Sciences
|
May 1, 1988
Infantile Refsum's disease: a generalized peroxisomal disorder. Case report with postmortem examination
A Torvik, S Torp, B F Kase, et al.
Pediatric Research
|
January 1, 1991
Importance of peroxisomes in the formation of chenodeoxycholic acid in human liver. Metabolism of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid in Zellweger syndrome
B F Kase, J I Pedersen, K O Wathne, et al.
The Biochemical Journal
|
October 21, 1999
Sulphation of lithocholic acid in the colon-carcinoma cell line CaCo-2
B Halvorsen, B F Kase, K Prydz, et al.
Human Genetics
|
February 1, 1996
Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndrome
T C Olsen, H G Eiken, P M Knappskog, et al.
Biochimica Et Biophysica Acta
|
August 15, 1984
Urinary excretion of dicarboxylic acids from patients with the Zellweger syndrome. Importance of peroxisomes in beta-oxidation of dicarboxylic acids
I Björkhem, S Blomstrand, P Hågå, et al.
Clinical Chemistry
|
August 21, 2004
Screening for serum total homocysteine in newborn children
Helga Refsum, Anne W Grindflek, Per M Ueland, et al.
Clinical Chemistry
|
August 6, 2000
Evaluation of novel assays in clinical chemistry: quantification of plasma total homocysteine
E Nexo, F Engbaek, P M Ueland, et al.
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of 7