Isolation and Characterization of Peroxisome-Deficient Chinese Hamster Ovary Cell Mutants Representing Human Complementation Group III

This publication has 29 references indexed in Scilit:

• A unified nomenclature for peroxisome biogenesis factors.
  The Journal of cell biology, 1996
• Peroxisomal assembly defects: Clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group
  The Journal of Pediatrics, 1995
• Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.
  Journal of Clinical Investigation, 1992
• BIOCHEMISTRY OF PEROXISOMES
  Annual Review of Biochemistry, 1992
• Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells
  Human Genetics, 1992
• A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly
  Science, 1992
• Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant
  Nature, 1991
• Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes.
  The Journal of cell biology, 1990
• Genetic and Phenotypic Heterogeneity in Disorders of Peroxisome Biogenesis—A Complementation Study Involving Cell Lines from 19 Patients
  Pediatric Research, 1989
• Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
  Journal of Clinical Investigation, 1988