1996) Peroxisome biogenesis in the yeast Hansenula polymorpha: a structural and functional analysis.
2001) The peroxin Pex6p gene is impaired in peroxisome biogenesis disorders of complementation group 6.
2004) Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene.
1996) A unified nomenclature for peroxisome biogenesis factors.
2000) The peroxin Pex3p initiates membrane assembly in peroxisome biogenesis.
1997) Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.
1997) Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders.
1995) Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders.
1996) The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.
1997) Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders.
2005) Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.
2001) Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.