Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency

Author:

Abe Yuichi,Honsho Masanori,Nakanishi Hiroki,Taguchi Ryo,Fujiki Yukio

Funder

Science and Technology Agency of Japan

Grants-in-Aid for Scientific Research

Global COE Program

Ministry of Education, Culture, Sports, Science and Technology of Japan

Kyushu University Interdisciplinary Programs in Education and Projects in Research Development

Takeda Science Foundation

Japanese Foundation for Applied Enzymology

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference57 articles.

1. Peroxisomes, lipid metabolism, and peroxisomal disorders;Wanders;Mol. Genet. Metab.,2004

2. Biochemistry of mammalian peroxisomes revisited;Wanders;Annu. Rev. Biochem.,2006

3. Peroxisome biogenesis disorders;Steinberg;Biochim. Biophys. Acta, Mol. Cell Res.,2006

4. Metabolic and molecular basis of peroxisomal disorders: a review;Wanders;Am. J. Med. Genet. A,2004

5. Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants;Fujiki;Biochim. Biophys. Acta, Mol. Cell Res.,2006

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