van Roermund CW - Search Results

1

Wanders RJ, Visser WF, van Roermund CW, Kemp S, Waterham HR. Wanders RJ, et al. Among authors: van roermund cw. Pflugers Arch. 2007 Feb;453(5):719-34. doi: 10.1007/s00424-006-0142-x. Epub 2006 Oct 13. Pflugers Arch. 2007. PMID: 17039367 Review.

2

Subcellular localization of squalene synthase in human hepatoma cell line Hep G2.

Cohen LH, Griffioen M, van Roermund CW, Wanders RJ. Cohen LH, et al. Among authors: van roermund cw. Biochim Biophys Acta. 1992 Jun 5;1126(1):114-8. doi: 10.1016/0005-2760(92)90224-j. Biochim Biophys Acta. 1992. PMID: 1318747

3

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.

Wanders RJ, van Roermund CW, Brul S, Schutgens RB, Tager JM. Wanders RJ, et al. Among authors: van roermund cw. J Inherit Metab Dis. 1992;15(3):385-8. doi: 10.1007/BF02435983. J Inherit Metab Dis. 1992. PMID: 1357231 No abstract available.

4

Molecular analysis of disorders of peroxisomal beta-oxidation.

Wanders RJ, van Roermund CW, Denis S, Schutgens RB, Ijlst L, Tager JM. Wanders RJ, et al. Among authors: van roermund cw. Prog Clin Biol Res. 1992;375:507-19. Prog Clin Biol Res. 1992. PMID: 1438395 Review. No abstract available.

5

X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect.

Wanders RJ, van Roermund CW, Lageweg W, Jakobs BS, Schutgens RB, Nijenhuis AA, Tager JM. Wanders RJ, et al. Among authors: van roermund cw. J Inherit Metab Dis. 1992;15(4):634-44. doi: 10.1007/BF01799620. J Inherit Metab Dis. 1992. PMID: 1528022 Review.

6

Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liver.

Wanders RJ, Denis S, van Roermund CW, Jakobs C, ten Brink HJ. Wanders RJ, et al. Among authors: van roermund cw. Biochim Biophys Acta. 1992 May 8;1125(3):274-9. doi: 10.1016/0005-2760(92)90056-2. Biochim Biophys Acta. 1992. PMID: 1596515

7

Peroxisomal enzyme activities in the human hepatoblastoma cell line HepG2 as compared to human liver.

Wanders RJ, van Roermund CW, Griffioen M, Cohen L. Wanders RJ, et al. Among authors: van roermund cw. Biochim Biophys Acta. 1991 Nov 14;1115(1):54-9. doi: 10.1016/0304-4165(91)90011-5. Biochim Biophys Acta. 1991. PMID: 1659911

8

Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.

van Roermund CW, Brul S, Tager JM, Schutgens RB, Wanders RJ. van Roermund CW, et al. J Inherit Metab Dis. 1991;14(2):152-64. doi: 10.1007/BF01800588. J Inherit Metab Dis. 1991. PMID: 1679469

9

Identification of pristanoyl-CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: implications for Zellweger syndrome.

Wanders RJ, van Roermund CW, Jakobs C, ten Brink HJ. Wanders RJ, et al. Among authors: van roermund cw. J Inherit Metab Dis. 1991;14(3):349-52. doi: 10.1007/BF01811700. J Inherit Metab Dis. 1991. PMID: 1770789 No abstract available.

10

Di- and trihydroxycholestanaemia in twin sisters.

Wanders RJ, van Roermund CW, Schelen A, Schutgens RB, Zeman J, Kozich V, Hyanek J, Casteels M, Mannaerts GP. Wanders RJ, et al. Among authors: van roermund cw. J Inherit Metab Dis. 1991;14(3):357-60. doi: 10.1007/BF01811702. J Inherit Metab Dis. 1991. PMID: 1770791 No abstract available.

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