Molecular defects in genetic diseases of peroxisomes
- 1 October 1997
- journal article
- review article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1361 (3), 235-250
- https://doi.org/10.1016/s0925-4439(97)00051-3
Abstract
No abstract availableFunding Information
- Nagase Science Technology Foundation
- Ministry of Education, Culture, Sports, Science and Technology
- Core Research for Evolutional Science and Technology
- Uehara Memorial Foundation
- Japan Science and Technology Corporation
- Mitsubishi Foundation
This publication has 84 references indexed in Scilit:
- Isolation and Characterization of Peroxisome-Deficient Chinese Hamster Ovary Cell Mutants Representing Human Complementation Group IIIExperimental Cell Research, 1997
- Isolation of a New Peroxisome-Deficient CHO Cell Mutant Defective in Peroxisome Targeting Signal-1 ReceptorBiochemical and Biophysical Research Communications, 1997
- Proteins involved in peroxisome biogenesis and functioningBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1996
- Peroxisome assembly factor–2, a putative ATPase cloned by functional complementation on a peroxisome–deficient mammalian cell mutantNature Genetics, 1995
- 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
- Adrenoleukodystrophy: The Restoration of Peroxisomal β-Oxidaton by Transfection of Normal cDNABiochemical and Biophysical Research Communications, 1995
- Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targetingBiochemical and Biophysical Research Communications, 1991
- Molecular analysis of human acatalasemiaJournal of Molecular Biology, 1990
- An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.The Journal of cell biology, 1989