Brul S - 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: brul s. Prog Clin Biol Res. 1990;321:545-58. Prog Clin Biol Res. 1990. PMID: 2183242

2

A procedure for selecting mammalian cells with an impairment in oxidative phosphorylation.

Lombardo MC, van der Zwaan JW, Brul S, Tager JM. Lombardo MC, et al. Among authors: brul s. Biochim Biophys Acta. 1992 Apr 14;1138(4):275-81. doi: 10.1016/0925-4439(92)90004-7. Biochim Biophys Acta. 1992. PMID: 1314097

3

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.

Wanders RJ, van Roermund CW, Brul S, Schutgens RB, Tager JM. Wanders RJ, et al. Among authors: brul s. J Inherit Metab Dis. 1992;15(3):385-8. doi: 10.1007/BF02435983. J Inherit Metab Dis. 1992. PMID: 1357231 No abstract available.

4

Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.

van Roermund CW, Brul S, Tager JM, Schutgens RB, Wanders RJ. van Roermund CW, et al. Among authors: brul s. J Inherit Metab Dis. 1991;14(2):152-64. doi: 10.1007/BF01800588. J Inherit Metab Dis. 1991. PMID: 1679469

5

Comparative study on glucocerebrosidase in spleens from patients with Gaucher disease.

Aerts JM, Donker-Koopman WE, Brul S, Van Weely S, Sa Miranda MC, Barranger JA, Tager JM, Schram AW. Aerts JM, et al. Among authors: brul s. Biochem J. 1990 Jul 1;269(1):93-100. doi: 10.1042/bj2690093. Biochem J. 1990. PMID: 2198026 Free PMC article.

6

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. J Clin Invest. 1988 Jun;81(6):1710-5. doi: 10.1172/JCI113510. J Clin Invest. 1988. PMID: 2454948 Free PMC article.

7

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: brul s. J Inherit Metab Dis. 1989;12 Suppl 2:301-4. doi: 10.1007/BF03335405. J Inherit Metab Dis. 1989. PMID: 2512431 No abstract available.

8

Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.

Wiemer EA, Brul S, Just WW, Van Driel R, Brouwer-Kelder E, Van Den Berg M, Weijers PJ, Schutgens RB, Van Den Bosch H, Schram A, et al. Wiemer EA, et al. Among authors: brul s. Eur J Cell Biol. 1989 Dec;50(2):407-17. Eur J Cell Biol. 1989. PMID: 2697558

9

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. 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

10

Efficient routing of glucocerebrosidase to lysosomes requires complex oligosaccharide chain formation.

Aerts JM, Brul S, Donker-Koopman WE, van Weely S, Murray GJ, Barranger JA, Tager JM, Schram AW. Aerts JM, et al. Among authors: brul s. Biochem Biophys Res Commun. 1986 Dec 15;141(2):452-8. doi: 10.1016/s0006-291x(86)80194-2. Biochem Biophys Res Commun. 1986. PMID: 2948505

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