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

982 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: wanders rj. 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.
Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomes.
Wanders RJ, Denis S, Jakobs C, ten Brink HJ. Wanders RJ, et al. Biochim Biophys Acta. 1992 Mar 4;1124(2):199-202. doi: 10.1016/0005-2760(92)90099-h. Biochim Biophys Acta. 1992. PMID: 1347460
Subcellular localisation and processing of non-specific lipid transfer protein are not aberrant in Rhizomelic Chondrodysplasia Punctata fibroblasts.
Heikoop JC, Ossendorp BC, Wanders RJ, Wirtz KW, Tager JM. Heikoop JC, et al. Among authors: wanders rj. FEBS Lett. 1992 Mar 9;299(2):201-4. doi: 10.1016/0014-5793(92)80247-e. FEBS Lett. 1992. PMID: 1347505
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. J Inherit Metab Dis. 1992;15(3):385-8. doi: 10.1007/BF02435983. J Inherit Metab Dis. 1992. PMID: 1357231 No abstract available.
Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidation.
Wanders RJ, IJlst L, Poggi F, Bonnefont JP, Munnich A, Brivet M, Rabier D, Saudubray JM. Wanders RJ, et al. Biochem Biophys Res Commun. 1992 Nov 16;188(3):1139-45. doi: 10.1016/0006-291x(92)91350-y. Biochem Biophys Res Commun. 1992. PMID: 1445348
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect.
Wanders RJ, van Roermund CW, Lageweg W, Jakobs BS, Schutgens RB, Nijenhuis AA, Tager JM. Wanders RJ, et al. J Inherit Metab Dis. 1992;15(4):634-44. doi: 10.1007/BF01799620. J Inherit Metab Dis. 1992. PMID: 1528022 Review.
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: wanders rj. Biochim Biophys Acta. 1991 Jul 26;1097(1):62-70. doi: 10.1016/0925-4439(91)90025-5. Biochim Biophys Acta. 1991. PMID: 1677591
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: wanders rj. J Inherit Metab Dis. 1991;14(2):152-64. doi: 10.1007/BF01800588. J Inherit Metab Dis. 1991. PMID: 1679469
Identification of superoxide dismutase in rat liver peroxisomes.
Wanders RJ, Denis S. Wanders RJ, et al. Biochim Biophys Acta. 1992 Jan 23;1115(3):259-62. doi: 10.1016/0304-4165(92)90063-z. Biochim Biophys Acta. 1992. PMID: 1739741
Identification of pristanoyl-CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: implications for Zellweger syndrome.
Wanders RJ, van Roermund CW, Jakobs C, ten Brink HJ. Wanders RJ, et al. J Inherit Metab Dis. 1991;14(3):349-52. doi: 10.1007/BF01811700. J Inherit Metab Dis. 1991. PMID: 1770789 No abstract available.
982 results
Jump to page
Feedback