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Pediatric Research|May 1, 1993
Analysis of peroxisomes in lymphoblasts: Zellweger syndrome and a patient with a deletion in chromosome 7M J Santos, A B Moser, H Drwinga, et al.
Molecular and Cellular Biology|January 1, 1994
Addition of lipid substituents of mammalian protein glycosylphosphoinositol anchorsN Singh, R A Zoeller, M L Tykocinski, et al.
Journal of Cellular Physiology|April 1, 1992
Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndromeM J Santos, S Hoefler, A B Moser, et al.
Biology of the Cell|July 6, 2000
Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger syndrome: a confocal laser scanning microscopy studyM J Santos, S C Henderson, A B Moser, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophyG M Small, M J Santos, T Imanaka, et al.
Pediatric Research|December 1, 1985
Zellweger syndrome: biochemical and morphological studies on two patients treated with clofibrateP B Lazarow, V Black, H Shio, et al.
Pediatric Research|July 1, 1988
Zellweger syndrome amniocytes: morphological appearance and a simple sedimentation method for prenatal diagnosisP B Lazarow, G M Small, M Santos, et al.
The Journal of Biological Chemistry|December 25, 1989
Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndromeR A Zoeller, L A Allen, M J Santos, et al.
Science (New York, N.Y.)|January 4, 1985
Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophiesS Goldfischer, J Collins, I Rapin, et al.
The Journal of Biological Chemistry|April 25, 1992
Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomesR A Zoeller, S Rangaswamy, H Herscovitz, et al.
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