Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

204 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Biochemistry of peroxisomes.
van den Bosch H, Schutgens RB, Wanders RJ, Tager JM. van den Bosch H, et al. Among authors: schutgens rb. 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.
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course.
Barth PG, Wanders RJ, Schutgens RB, Bleeker-Wagemakers EM, van Heemstra D. Barth PG, et al. Among authors: schutgens rb. Eur J Pediatr. 1990 Jul;149(10):722-6. doi: 10.1007/BF01959531. Eur J Pediatr. 1990. PMID: 2209666
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: schutgens rb. J Inherit Metab Dis. 1988;11 Suppl 2:173-7. doi: 10.1007/BF01804228. J Inherit Metab Dis. 1988. PMID: 3141702 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: schutgens rb. J Inherit Metab Dis. 1988;11 Suppl 2:161-4. doi: 10.1007/BF01804225. J Inherit Metab Dis. 1988. PMID: 3141699 No abstract available.
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: schutgens rb. J Inherit Metab Dis. 1989;12 Suppl 2:301-4. doi: 10.1007/BF03335405. J Inherit Metab Dis. 1989. PMID: 2512431 No abstract available.
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: schutgens rb. J Inherit Metab Dis. 1991;14(2):152-64. doi: 10.1007/BF01800588. J Inherit Metab Dis. 1991. PMID: 1679469
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: schutgens rb. J Inherit Metab Dis. 1992;15(3):385-8. doi: 10.1007/BF02435983. J Inherit Metab Dis. 1992. PMID: 1357231 No abstract available.
Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.
van den Bosch H, Schalkwijk CG, Schrakamp G, Wanders RJ, Schutgens RB, Schram AW, Tager JM. van den Bosch H, et al. Among authors: schutgens rb. Prog Clin Biol Res. 1988;282:139-50. Prog Clin Biol Res. 1988. PMID: 3071794 Review.
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: schutgens rb. Prog Clin Biol Res. 1990;321:545-58. Prog Clin Biol Res. 1990. PMID: 2183242
Ether lipid synthesis and its deficiency in peroxisomal disorders.
van den Bosch H, Schrakamp G, Hardeman D, Zomer AW, Wanders RJ, Schutgens RB. van den Bosch H, et al. Among authors: schutgens rb. Biochimie. 1993;75(3-4):183-9. doi: 10.1016/0300-9084(93)90076-5. Biochimie. 1993. PMID: 8507680 Review.
204 results
Jump to page
Feedback