Peroxisomes in human fibroblasts have a basic pH

This publication has 16 references indexed in Scilit:

• Peroxisomal disorders: clinical, biochemical, and molecular aspects.
  Neurochemical Research, 1999
• Lipid metabolism in peroxisomes in relation to human disease
  Molecular Aspects of Medicine, 1998
• IDP3 Encodes a Peroxisomal NADP-dependent Isocitrate Dehydrogenase Required for the β-Oxidation of Unsaturated Fatty Acids
  Journal of Biological Chemistry, 1998
• Components Involved in Peroxisome Import, Biogenesis, Proliferation, Turnover, and Movement
  Physiological Reviews, 1998
• Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
  Nature Genetics, 1997
• Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor.
  The Journal of cell biology, 1996
• The membrane of peroxisomes in Saccharomyces cerevisiae is impermeable to NAD(H) and acetyl-CoA under in vivo conditions.
  The EMBO Journal, 1995
• Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
  Nature Genetics, 1995
• BIOCHEMISTRY OF PEROXISOMES
  Annual Review of Biochemistry, 1992
• A conserved tripeptide sorts proteins to peroxisomes.
  The Journal of cell biology, 1989