In Vitro Transport of Membrane Proteins to Peroxisomes by Shuttling Receptor Pex19p
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference42 articles.
1. THE GENETICS OF PEROXISOME BIOGENESIS
2. Peroxisome biogenesis and peroxisome biogenesis disorders
3. Peroxisome biogenesis: advances and conundrums
4. Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
5. Newly Identified Chinese Hamster Ovary Cell Mutants Are Defective in Biogenesis of Peroxisomal Membrane Vesicles (Peroxisomal Ghosts), Representing a Novel Complementation Group in Mammals
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1. Molecular insights into peroxisome homeostasis and peroxisome biogenesis disorders;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2022-11
2. De novo formation and maintenance of mammalian peroxisomes in the absence of PEX16;Journal of Cell Science;2022-04-19
3. Recognition and Chaperoning by Pex19, Followed by Trafficking and Membrane Insertion of the Peroxisome Proliferation Protein, Pex11;Cells;2022-01-04
4. Identification of Pex34p as a component of the peroxisomal de novo biogenesis machinery in yeast;2021-05-31
5. Peroxisomal fission is modulated by the mitochondrial Rho‐GTPases, Miro1 and Miro2;EMBO reports;2020-01-02
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