The Human PEX3 Gene Encoding a Peroxisomal Assembly Protein: Genomic Organization, Positional Mapping, and Mutation Analysis in Candidate Phenotypes
- 1 February 2000
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 268 (3) , 704-710
- https://doi.org/10.1006/bbrc.2000.2193
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- Pex17p Is Required for Import of Both Peroxisome Membrane and Lumenal Proteins and Interacts with Pex19p and the Peroxisome Targeting Signal–Receptor Docking Complex inPichia pastorisMolecular Biology of the Cell, 1999
- Genotype–Phenotype Correlations in Disorders of Peroxisome BiogenesisMolecular Genetics and Metabolism, 1999
- Identification and characterization of the human peroxin PEX3European Journal of Cell Biology, 1999
- Pex19p Interacts with Pex3p and Pex10p and Is Essential for Peroxisome Biogenesis inPichia pastorisMolecular Biology of the Cell, 1999
- Pex19p, a Farnesylated Protein Essential for Peroxisome BiogenesisMolecular and Cellular Biology, 1998
- A unified nomenclature for peroxisome biogenesis factors.The Journal of cell biology, 1996
- The Hansenula polymorpha PER9 Gene Encodes a Peroxisomal Membrane Protein Essential for Peroxisome Assembly and IntegrityJournal of Biological Chemistry, 1996
- BIOCHEMISTRY OF PEROXISOMESAnnual Review of Biochemistry, 1992
- Isolation of peroxisome-deficient mutants of Saccharomyces cerevisiae.Proceedings of the National Academy of Sciences, 1989
- Metabolic Pathways in Peroxisomes and GlyoxysomesAnnual Review of Biochemistry, 1981