Genomic Organization and Characterization of Human PEX2 Encoding a 35-kDa Peroxisomal Membrane Protein

This publication has 36 references indexed in Scilit:

• Transmembrane topology of the peroxin, Pex2p, an essential component for the peroxisome assembly.
  The Journal of Biochemistry, 1999
• Human PEX19 : cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
  Proceedings of the National Academy of Sciences, 1999
• Peroxisome Synthesis in the Absence of Preexisting Peroxisomes
  The Journal of cell biology, 1999
• A nonmammalian homolog of the PAF7 gene(Zellweger syndrome) discovered as a gene involved in caryogamy in the fungus Podospora anserina
  Cell, 1995
• Identification and preliminary characterization of a protein motif related to the zinc finger.
  Proceedings of the National Academy of Sciences, 1993
• A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly
  Science, 1992
• Targeting of proteins into the peroxisomal matrix
  The Journal of Membrane Biology, 1992
• A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase.
  The EMBO Journal, 1991
• Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant
  Nature, 1991
• A conserved tripeptide sorts proteins to peroxisomes.
  The Journal of cell biology, 1989