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Biochemistry of peroxisomes.
van den Bosch H, Schutgens RB, Wanders RJ, Tager JM. van den Bosch H, et al. Among authors: tager jm. Annu Rev Biochem. 1992;61:157-97. doi: 10.1146/annurev.bi.61.070192.001105. Annu Rev Biochem. 1992. PMID: 1353950 Review. No abstract available.
X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts.
Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Schram AW, Tager JM, van den Bosch H, Schalkwijk C. Wanders RJ, et al. Among authors: tager jm. J Inherit Metab Dis. 1988;11 Suppl 2:173-7. doi: 10.1007/BF01804228. J Inherit Metab Dis. 1988. PMID: 3141702 No abstract available.
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. Prog Clin Biol Res. 1990;321:545-58. Prog Clin Biol Res. 1990. PMID: 2183242
Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids.
Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, van den Bosch H, Schram AW, Tager JM. Wanders RJ, et al. Among authors: tager jm. Biochem Biophys Res Commun. 1988 Jun 16;153(2):618-24. doi: 10.1016/s0006-291x(88)81140-9. Biochem Biophys Res Commun. 1988. PMID: 3382393
Prenatal diagnosis of Zellweger syndrome by direct visualization of peroxisomes in chorionic villus fibroblasts by immunofluorescence microscopy.
Wanders RJ, Wiemer EA, Brul S, Schutgens RB, van den Bosch H, Tager JM. Wanders RJ, et al. Among authors: tager jm. J Inherit Metab Dis. 1989;12 Suppl 2:301-4. doi: 10.1007/BF03335405. J Inherit Metab Dis. 1989. PMID: 2512431 No abstract available.
Long-chain-acyl-CoA synthetase and very-long-chain-acyl-CoA synthetase activities in peroxisomes and microsomes from rat liver. An enzymological study.
Lageweg W, Wanders RJ, Tager JM. Lageweg W, et al. Among authors: tager jm. Eur J Biochem. 1991 Mar 14;196(2):519-23. doi: 10.1111/j.1432-1033.1991.tb15844.x. Eur J Biochem. 1991. PMID: 2007410
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: tager jm. 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
Nucleotide sequence of human peroxisomal 3-oxoacyl-CoA thiolase.
Bout A, Teunissen Y, Hashimoto T, Benne R, Tager JM. Bout A, et al. Among authors: tager jm. Nucleic Acids Res. 1988 Nov 11;16(21):10369. doi: 10.1093/nar/16.21.10369. Nucleic Acids Res. 1988. PMID: 3194209 Free PMC article. No abstract available.
Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia.
Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Tager JM, van den Bosch H, Thomas GH. Wanders RJ, et al. Among authors: tager jm. J Inherit Metab Dis. 1988;11 Suppl 2:161-4. doi: 10.1007/BF01804225. J Inherit Metab Dis. 1988. PMID: 3141699 No abstract available.
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23.
Bout A, Hoovers JM, Bakker E, Mannens MM, Geurts van Kessel A, Westerveld A, Tager JM, Benne R. Bout A, et al. Among authors: tager jm. Cytogenet Cell Genet. 1989;52(3-4):147-50. doi: 10.1159/000132865. Cytogenet Cell Genet. 1989. PMID: 2630187
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