Heikoop JC - Search Results

1

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.

2

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

3

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

4

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.

5

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder.

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

6

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. J Clin Invest. 1987 Dec;80(6):1778-83. doi: 10.1172/JCI113271. J Clin Invest. 1987. PMID: 3680527 Free PMC article.

7

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

8

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.

9

Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata.

Espeel M, Heikoop JC, Smeitink JA, Beemer FA, De Craemer D, Van den Berg M, Hashimoto T, Wanders RJ, Schutgens RB, Poll-The BT, et al. Espeel M, et al. Among authors: heikoop jc. Ultrastruct Pathol. 1993 Nov-Dec;17(6):623-36. doi: 10.3109/01913129309027798. Ultrastruct Pathol. 1993. PMID: 8122328

10

Subcellular fractionation of cultured normal human melanocytes: new insights into the relationship of melanosomes with lysosomes and peroxisomes.

Smit NP, van Roermund CW, Aerts HM, Heikoop JC, Van den Berg M, Pavel S, Wanders RJ. Smit NP, et al. Among authors: heikoop jc. Biochim Biophys Acta. 1993 Mar 24;1181(1):1-6. doi: 10.1016/0925-4439(93)90082-c. Biochim Biophys Acta. 1993. PMID: 8457599

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