Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent
Author:
Publisher
Wiley
Subject
Cell Biology,Clinical Biochemistry,General Medicine,Biochemistry
Reference29 articles.
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2. Peroxisome biogenesis disorders;Weller;Annu Rev Genomics Hum Genet,2003
3. The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes;Matsumoto;Nat Cell Biol,2003
4. Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants;Fujiki;Biochim Biophys Acta,2006
5. Biogenesis of peroxisomes;Lazarow;Annu Rev Cell Biol,1985
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4. Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2014-04
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