Heikoop J - Search Results

1

Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cells.

Aerts JM, Heikoop J, van Weely S, Donker-Koopman WE, Barranger JA, Tager JM, Schram AW. Aerts JM, et al. Among authors: heikoop j. Exp Cell Res. 1988 Aug;177(2):391-8. doi: 10.1016/0014-4827(88)90472-7. Exp Cell Res. 1988. PMID: 3391250

2

Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolase.

Van Weely S, Aerts JM, Van Leeuwen MB, Heikoop JC, Donker-Koopman WE, Barranger JA, Tager JM, Schram AW. Van Weely S, et al. Among authors: heikoop jc. Eur J Biochem. 1990 Aug 17;191(3):669-77. doi: 10.1111/j.1432-1033.1990.tb19173.x. Eur J Biochem. 1990. PMID: 2143986 Free article.

3

Turnover of peroxisomal vesicles by autophagic proteolysis in cultured fibroblasts from Zellweger patients.

Heikoop JC, van den Berg M, Strijland A, Weijers PJ, Just WW, Meijer AJ, Tager JM. Heikoop JC, et al. Eur J Cell Biol. 1992 Apr;57(2):165-71. Eur J Cell Biol. 1992. PMID: 1511694

4

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder.

Wanders RJ, Schumacher H, Heikoop J, Schutgens RB, Tager JM. Wanders RJ, et al. Among authors: heikoop j. J Inherit Metab Dis. 1992;15(3):389-91. doi: 10.1007/BF02435984. J Inherit Metab Dis. 1992. PMID: 1405476 No abstract available.

5

Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.

Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Heikoop J, van den Bosch H, Schram AW, Tager JM. Wanders RJ, et al. Among authors: heikoop j. J Clin Invest. 1987 Dec;80(6):1778-83. doi: 10.1172/JCI113271. J Clin Invest. 1987. PMID: 3680527 Free PMC article.

6

Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts.

Heikoop JC, Van den Berg M, Strijland A, Weijers PJ, Schutgens RB, Just WW, Wanders RJ, Tager JM. Heikoop JC, et al. Biochim Biophys Acta. 1991 Jul 26;1097(1):62-70. doi: 10.1016/0925-4439(91)90025-5. Biochim Biophys Acta. 1991. PMID: 1677591

7

Subcellular localisation and processing of non-specific lipid transfer protein are not aberrant in Rhizomelic Chondrodysplasia Punctata fibroblasts.

Heikoop JC, Ossendorp BC, Wanders RJ, Wirtz KW, Tager JM. Heikoop JC, et al. FEBS Lett. 1992 Mar 9;299(2):201-4. doi: 10.1016/0014-5793(92)80247-e. FEBS Lett. 1992. PMID: 1347505 Free article.

8

Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation study.

Heikoop JC, Wanders RJ, Strijland A, Purvis R, Schutgens RB, Tager JM. Heikoop JC, et al. Hum Genet. 1992 Jun;89(4):439-44. doi: 10.1007/BF00194319. Hum Genet. 1992. PMID: 1618493

9

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.

Heikoop JC, van Roermund CW, Just WW, Ofman R, Schutgens RB, Heymans HS, Wanders RJ, Tager JM. Heikoop JC, et al. J Clin Invest. 1990 Jul;86(1):126-30. doi: 10.1172/JCI114674. J Clin Invest. 1990. PMID: 2365812 Free PMC article.

10

Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.

Wanders RJ, van Roermund CW, van Wijland MJ, Heikoop J, Schutgens RB, Schram AW, Tager JM, van den Bosch H, Poll-Thé BT, Saudubray JM, et al. Wanders RJ, et al. Among authors: heikoop j. Clin Chim Acta. 1987 Jul 15;166(2-3):255-63. doi: 10.1016/0009-8981(87)90428-1. Clin Chim Acta. 1987. PMID: 2441904

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