Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts
- 1 December 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (6) , 1898-1906
- https://doi.org/10.1086/302142
Abstract
No abstract availableKeywords
Funding Information
- Ono Medical Research Foundation
- National Center of Neurology and Psychiatry
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
This publication has 28 references indexed in Scilit:
- Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disordersNature Genetics, 1997
- Mutations in PEX1 are the most common cause of peroxisome biogenesis disordersNature Genetics, 1997
- Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor.The Journal of cell biology, 1996
- Isolation and Characterization of Pas2p, a Peroxisomal Membrane Protein Essential for Peroxisome Biogenesis in the Methylotrophic Yeast Pichia pastorisPublished by Elsevier ,1996
- The Hansenula polymorpha PER9 Gene Encodes a Peroxisomal Membrane Protein Essential for Peroxisome Assembly and IntegrityJournal of Biological Chemistry, 1996
- Peroxisomal assembly defects: Clinical, pathologic, and biochemical findings in two patients in a newly identified complementation groupThe Journal of Pediatrics, 1995
- Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groupsThe Journal of Pediatrics, 1995
- Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders.Journal of Clinical Investigation, 1993
- Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.Journal of Clinical Investigation, 1992
- Peroxisome assembly mutations in humans: Structural heterogeneity in Zellweger syndromeJournal of Cellular Physiology, 1992