PEX13 Is Mutated in Complementation Group 13 of the Peroxisome-Biogenesis Disorders
Open Access
- 1 September 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (3) , 621-634
- https://doi.org/10.1086/302534
Abstract
No abstract availableKeywords
This publication has 58 references indexed in Scilit:
- Characterization of PECI, a Novel Monofunctional Δ3,Δ2-Enoyl-CoA Isomerase of Mammalian PeroxisomesJournal of Biological Chemistry, 1999
- Involvement of Pex13p in Pex14p Localization and Peroxisomal Targeting Signal 2–dependent Protein Import into PeroxisomesThe Journal of cell biology, 1999
- Expression of PEX11β Mediates Peroxisome Proliferation in the Absence of Extracellular StimuliJournal of Biological Chemistry, 1998
- Peroxisome biogenesis: Back to the endoplasmic reticulum?Current Biology, 1998
- Identification of PAHX, a Refsum disease geneNature 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
- The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import PTS1-containing proteins.The Journal of cell biology, 1996
- Sequence of a putative human housekeeping gene (HK33) localized on chromosome 1Gene, 1994
- High-resolution crystal structures of tyrosine kinase SH3 domains complexed with proline-rich peptidesNature Structural & Molecular Biology, 1994
- Protein Import into Peroxisomes and Biogenesis of the OrganelleAnnual Review of Cell Biology, 1993