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Page 1
Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome.
Tager JM, Van der Beek WA, Wanders RJ, Hashimoto T, Heymans HS, Van den Bosch H, Schutgens RB, Schram AW. Tager JM, et al. Among authors: van den bosch h, van der beek wa. Biochem Biophys Res Commun. 1985 Feb 15;126(3):1269-75. doi: 10.1016/0006-291x(85)90322-5. Biochem Biophys Res Commun. 1985. PMID: 3977916
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
Schram AW, Goldfischer S, van Roermund CW, Brouwer-Kelder EM, Collins J, Hashimoto T, Heymans HS, van den Bosch H, Schutgens RB, Tager JM, et al. Schram AW, et al. Among authors: van roermund cw, van den bosch h. Proc Natl Acad Sci U S A. 1987 Apr;84(8):2494-6. doi: 10.1073/pnas.84.8.2494. Proc Natl Acad Sci U S A. 1987. PMID: 2882519 Free PMC article.
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: van den bosch h. 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
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders.
Wanders RJ, van Wijland MJ, van Roermund CW, Schutgens RB, van den Bosch H, Tager JM, Nijenhuis A, Tromp A. Wanders RJ, et al. Among authors: van roermund cw, van wijland mj, van den bosch h. Clin Chim Acta. 1987 Jun 15;165(2-3):303-10. doi: 10.1016/0009-8981(87)90175-6. Clin Chim Acta. 1987. PMID: 3652452
321 results