Strijland A - Search Results

1

Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.

Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A. Tager JM, et al. Among authors: strijland a. Prog Clin Biol Res. 1990;321:545-58. Prog Clin Biol Res. 1990. PMID: 2183242

2

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. Among authors: strijland a. Biochim Biophys Acta. 1991 Jul 26;1097(1):62-70. doi: 10.1016/0925-4439(91)90025-5. Biochim Biophys Acta. 1991. PMID: 1677591

3

Does aminotriazole inhibit import of catalase into peroxisomes by retarding unfolding?

Middelkoop E, Strijland A, Tager JM. Middelkoop E, et al. Among authors: strijland a. FEBS Lett. 1991 Feb 11;279(1):79-82. doi: 10.1016/0014-5793(91)80255-2. FEBS Lett. 1991. PMID: 1995347 Free article.

4

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.

Brul S, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, van den Bosch H, Tager JM. Brul S, et al. Among authors: strijland a. J Clin Invest. 1988 Jun;81(6):1710-5. doi: 10.1172/JCI113510. J Clin Invest. 1988. PMID: 2454948 Free PMC article.

5

Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders.

Brul S, Wiemer EA, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, Van den Bosch H, Tager JM. Brul S, et al. Among authors: strijland a. Biochem Biophys Res Commun. 1988 May 16;152(3):1083-9. doi: 10.1016/s0006-291x(88)80395-4. Biochem Biophys Res Commun. 1988. PMID: 3377768

6

Topology of catalase assembly in human skin fibroblasts.

Middelkoop E, Wiemer EA, Schoenmaker DE, Strijland A, Tager JM. Middelkoop E, et al. Among authors: strijland a. Biochim Biophys Acta. 1993 Dec 16;1220(1):15-20. doi: 10.1016/0167-4889(93)90091-3. Biochim Biophys Acta. 1993. PMID: 8268239

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. Among authors: strijland a. Eur J Cell Biol. 1992 Apr;57(2):165-71. Eur J Cell Biol. 1992. PMID: 1511694

8

Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.

Schram AW, Strijland A, Hashimoto T, Wanders RJ, Schutgens RB, van den Bosch H, Tager JM. Schram AW, et al. Among authors: strijland a. Proc Natl Acad Sci U S A. 1986 Aug;83(16):6156-8. doi: 10.1073/pnas.83.16.6156. Proc Natl Acad Sci U S A. 1986. PMID: 2426710 Free PMC article.

9

Catalase in cultured skin fibroblasts from patients with the cerebro-hepato-renal (Zellweger) syndrome: normal maturation in peroxisome-deficient cells.

Wanders RJ, Strijland A, van Roermund CW, van den Bosch H, Schutgens RB, Tager JM, Schram AW. Wanders RJ, et al. Among authors: strijland a. Biochim Biophys Acta. 1987 Mar 19;923(3):478-82. doi: 10.1016/0304-4165(87)90057-2. Biochim Biophys Acta. 1987. PMID: 3828388

10

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. Among authors: strijland a. Hum Genet. 1992 Jun;89(4):439-44. doi: 10.1007/BF00194319. Hum Genet. 1992. PMID: 1618493

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