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The Journal of Biological Chemistry|August 2, 2001
Multiple human vault RNAs. Expression and association with the vault complexA van Zon, M H Mossink, M Schoester, et al.
Biochimica Et Biophysica Acta|October 21, 1991
Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation groupE A Wiemer, M Out, A Schelen, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|October 23, 2001
Detection of the Mr 110,000 lung resistance-related protein LRP/MVP with monoclonal antibodiesA B Schroeijers, G L Scheffer, A W Reurs, et al.
The Journal of Cell Biology|July 1, 1995
Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disordersE A Wiemer, W M Nuttley, B L Bertolaet, et al.
Blood|May 23, 2001
MDR1 gene-related clonal selection and P-glycoprotein function and expression in relapsed or refractory acute myeloid leukemiaM M van den Heuvel-Eibrink, E A Wiemer, M J de Boevere, et al.
Progress in Clinical and Biological Research|January 1, 1990
Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomesJ M Tager, S Brul, E A Wiemer, et al.
Biochemical and Biophysical Research Communications|May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disordersS Brul, E A Wiemer, A Westerveld, et al.
European Journal of Cell Biology|December 1, 1989
Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghostsE A Wiemer, S Brul, W W Just, et al.
Leukemia|March 10, 2001
MDR1 expression in poor-risk acute myeloid leukemia with partial or complete monosomy 7M M van den Heuvel-Eibrink, E A Wiemer, M J de Boevere, et al.
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