Y. Fujiki

发表

PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p

T. Tsukamoto, N. Shimozawa, K. Okumoto, 1998, Molecular and Cellular Biology.

A unified nomenclature for peroxisome biogenesis factors

H. Moser, D. Valle, H. Tabak, 1996, The Journal of cell biology.

The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway

Y. Fujiki, T. Matsuzaki, 2008, The Journal of cell biology.

Molecular Basis for Peroxisome Biogenesis Disorders

K. Okumoto, S. Tamura, Y. Fujiki, 2014 .

New insights into dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p in shuttling of PTS1-receptor Pex5p during peroxisome biogenesis.

K. Okumoto, S. Tamura, Y. Fujiki, 2012, Biochimica et biophysica acta.

Impaired plasmalogen synthesis dysregulates liver X receptor-dependent transcription in cerebellum.

T. Uchiumi, D. Kang, Y. Fujiki, 2019, Journal of biochemistry.

Plasmalogen homeostasis – regulation of plasmalogen biosynthesis and its physiological consequence in mammals

Y. Fujiki, M. Honsho, 2017, FEBS letters.

Overexpression of human acyl-CoA thioesterase upregulates peroxisome biogenesis.

M. Miyazaki, Hiroyuki Watanabe, S. Yamasaki, 2004, Experimental cell research.

Pex5p Imports Folded Tetrameric Catalase by Interaction with Pex13p

Y. Fujiki, H. Otera, 2012, Traffic.

Peroxisome biogenesis and molecular defects in peroxisome assembly disorders

K. Okumoto, S. Tamura, Y. Fujiki, 2007, Cell Biochemistry and Biophysics.

Molecular defects in genetic diseases of peroxisomes.

Y. Fujiki, Yukio Fujiki, 1997, Biochimica et biophysica acta.

Peroxisome Deficiency Impairs BDNF Signaling and Memory

T. Yamashita, S. Tamura, Y. Fujiki, 2020, Frontiers in Cell and Developmental Biology.

Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis.

Y. Fujiki, Shinta Kobayashi, A. Tanaka, 2007, Experimental cell research.

Functional Domains and Dynamic Assembly of the Peroxin Pex14p, the Entry Site of Matrix Proteins*

Y. Fujiki, R. Itoh, 2006, Journal of Biological Chemistry.

Carboxyl-terminal consensus Ser-Lys-Leu-related tripeptide of peroxisomal proteins functions in vitro as a minimal peroxisome-targeting signal.

T. Hashimoto, S. Miyazawa, S. Miura, 1992, The Journal of biological chemistry.

A newly isolated Pex7‐binding, atypical PTS2 protein P7BP2 is a novel dynein‐type AAA+ protein

K. Noi, T. Ogura, K. Okumoto, 2018, Journal of biochemistry.

Peroxisome Biogenesis Disorders.

K. Okumoto, S. Tamura, Y. Fujiki, 2020, Advances in experimental medicine and biology.

Peroxisome: Metabolic Functions and Biogenesis.

K. Okumoto, S. Tamura, Y. Fujiki, 2020, Advances in experimental medicine and biology.

Assessing Pexophagy in Mammalian Cells.

Y. Fujiki, S. Yamashita, 2017, Methods in molecular biology.

Peroxisome biogenesis and human peroxisome-deficiency disorders

Y. Fujiki, 2016, Proceedings of the Japan Academy. Series B, Physical and biological sciences.

PEX 5 , and the affinity of LC 3-II for PEX 14 increases upon cell starvation

Y. Fujiki, S. Yamashita, K. Abe, 2014 .

The membrane peroxin PEX3 induces peroxisome-ubiquitination-linked pexophagy

Y. Fujiki, S. Yamashita, K. Abe, 2014, Autophagy.

Genetic and molecular bases of peroxisome biogenesis disorders

T. Tsukamoto, N. Shimozawa, T. Osumi, 2001, Genetics in Medicine.

Peroxisomal topogenic signals and the etiology of peroxisome-deficient disease

Y. Fujiki, 1996 .

Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus

S. Miyazawa, S. Miura, T. Osumi, 1989 .

Partial disassembly of peroxisomes

H. Shio, Y. Fujiki, P. Lazarow, 1985, The Journal of cell biology.

Experimental Systems to Study Yeast Pexophagy.

Y. Fujiki, Y. Sakai, Masahide Oku, 2017, Methods in molecular biology.

Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.

K. Ghaedi, A. Imamura, Y. Suzuki, 2000, Human molecular genetics.

Functional identification of AtAVT3, a family of vacuolar amino acid transporters, in Arabidopsis

Y. Fujiki, Y. Ohsumi, Y. Kakinuma, 2017, FEBS letters.

CUL4A-DDB1-Rbx1 E3 ligase controls the quality of the PTS2 receptor Pex7p.

Y. Fujiki, Kosuke Kuroda, S. Mukai, 2014, The Biochemical journal.

Mitotic phosphorylation of Pex14p regulates peroxisomal import machinery

H. Kosako, S. Tamura, Y. Fujiki, 2020, The Journal of cell biology.

Reduction of Ether-Type Glycerophospholipids, Plasmalogens, by NF-κB Signal Leading to Microglial Activation

Y. Fujiki, M. Honsho, Md Shamim Hossain, 2017, The Journal of Neuroscience.

Two Proteases, Trypsin Domain-containing 1 (Tysnd1) and Peroxisomal Lon Protease (PsLon), Cooperatively Regulate Fatty Acid β-Oxidation in Peroxisomal Matrix*

K. Okumoto, Y. Fujiki, Yukari Kametani, 2011, The Journal of Biological Chemistry.

Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants.

K. Ghaedi, K. Okumoto, Y. Fujiki, 2006, Biochimica et biophysica acta.

Peroxisome assembly and peroxisome biogenesis disorders

Y. Fujiki, 2002 .

Peroxisome biogenesis and peroxisome biogenesis disorders

Y. Fujiki, Yukio Fujiki, 2000, FEBS letters.

Molecular Anatomy of the Peroxin Pex12p

K. Okumoto, Y. Fujiki, I. Abe, 2000, The Journal of Biological Chemistry.

Peroxisome Targeting Signal Type 1 (PTS1) Receptor Is Involved in Import of Both PTS1 and PTS2: Studies withPEX5-Defective CHO Cell Mutants

T. Tsukamoto, K. Okumoto, T. Osumi, 1998, Molecular and Cellular Biology.

Mitochondrial phosphatidylethanolamine level modulates Cyt c oxidase activity to maintain respiration capacity in Arabidopsis thaliana rosette leaves.

Y. Fujiki, I. Nishida, J. Mizoi, 2013, Plant & cell physiology.

Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata

H. Waterham, R. Wanders, K. Ikeda, 2012, Journal of Lipid Research.

Parkin‐mediated ubiquitylation redistributes MITOL/March5 from mitochondria to peroxisomes

Keiji Tanaka, Y. Kimura, H. Kosako, 2019, EMBO reports.

Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis.

S. Tamura, Y. Fujiki, Non Miyata, 2008, Biochemical Society transactions.

Polypeptide and phospholipid composition of the membrane of rat liver peroxisomes: comparison with endoplasmic reticulum and mitochondrial membranes

H. Shio, Y. Fujiki, A. Hubbard, 1982, The Journal of cell biology.

Isolation and Characterization of cDNA Clones for the E1β and E2 Subunits of the Branched-chain α-Ketoacid Dehydrogenase Complex in Arabidopsis *

Masaki Ito, Y. Fujiki, A. Watanabe, 2000, The Journal of Biological Chemistry.

Molecular Complex Coordinating Peroxisome Morphogenesis in Mammalian Cells

Y. Fujiki, M. Honsho, Y. Abe, 2014 .

The × Gene of Hepatitis B Virus Induced Growth Stimulation and Tumorigenic Transformation of Mouse NIH3T3 Cells

K. Koike, Y. Fujiki, M. Oda, 1989, Japanese journal of cancer research : Gann.

ATP8B2-Mediated Asymmetric Distribution of Plasmalogens Regulates Plasmalogen Homeostasis and Plays a Role in Intracellular Signaling

Y. Fujiki, M. Honsho, S. Mawatari, 2022, Frontiers in Molecular Biosciences.

A peroxisome deficiency–induced reductive cytosol state up-regulates the brain-derived neurotrophic factor pathway

T. Yamashita, Y. Fujiki, Y. Sakai, 2020, The Journal of Biological Chemistry.

Homeostasis of Plasmalogens in Mammals

Y. Fujiki, M. Honsho, 2019, Encyclopedia of Food Chemistry.

Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant

T. Tsukamoto, S. Miura, Y. Fujiki, 1991, Nature.

Dysregulation of Plasmalogen Homeostasis Impairs Cholesterol Biosynthesis*

Y. Fujiki, M. Honsho, Y. Abe, 2015, The Journal of Biological Chemistry.

Fujiki Masanori Honsho , Yuichi Abe and Yukio impairs cholesterol biosynthesis Dysregulation of plasmalogen homeostasis

Y. Fujiki, M. Honsho, Y. Abe, 2015 .

Monomer-dimer transition of the conserved N-terminal domain of the mammalian peroxisomal matrix protein import receptor, Pex14p.

Jianrui Su, K. Miki, S. Tamura, 2010, Biochemical and biophysical research communications.

Molecular cloning of the aminopeptidase Y gene of Saccharomyces cerevisiae. Sequence analysis and gene disruption of a new aminopeptidase.

Y. Fujiki, T. Nakai, A. Ohashi, 1994, The Journal of biological chemistry.

Dynamic and Functional Assembly of the AAA Peroxins, Pex1p and Pex6p, and Their Membrane Receptor Pex26p*

S. Tamura, Y. Fujiki, N. Matsumoto, 2006, Journal of Biological Chemistry.

Molecular insights into peroxisome homeostasis and peroxisome biogenesis disorders.

K. Okumoto, Y. Fujiki, M. Honsho, 2022, Biochimica et biophysica acta. Molecular cell research.

Docosahexaenoic acid mediates peroxisomal elongation, a prerequisite for peroxisome division

A. Moser, Y. Fujiki, M. Honsho, 2012, Journal of Cell Science.

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

Mark R. Marten, Erinna F. Lee, Dana L. Miller, 2021, Autophagy.

Leucine and its keto acid enhance the coordinated expression of genes for branched‐chain amino acid catabolism in Arabidopsis under sugar starvation

Masaki Ito, Y. Fujiki, I. Nishida, 2001, FEBS letters.

Peroxin Pex14p is the key component for coordinated autophagic degradation of mammalian peroxisomes by direct binding to LC3‐II

Y. Fujiki, S. Yamashita, S. Hara-Kuge, 2015, Genes to cells : devoted to molecular & cellular mechanisms.

Recruitment of the RNA Helicase RHAU to Stress Granules via a Unique RNA-binding Domain*

Y. Nagamine, Y. Fujiki, F. Iwamoto, 2008, Journal of Biological Chemistry.

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.

R. Wanders, R. Wanders, T. Tsukamoto, 1999, Human molecular genetics.

Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.

R. Wanders, A. Imamura, Y. Suzuki, 1998, Biochemical and biophysical research communications.

UvA-DARE ( Digital Academic Repository ) Defective PEX gene products correlate with the protein import , biochemical abnormalities , and phenotypic heterogeneity in peroxisome biogenesis disorders

R. Wanders, G. Besley, T. Tsukamoto, 1999 .

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

H. Nakanishi, R. Taguchi, Y. Fujiki, 2014, Biochimica et biophysica acta.

AAA Peroxins and Their Recruiter Pex26p Modulate the Interactions of Peroxins Involved in Peroxisomal Protein Import*

S. Tamura, Y. Fujiki, N. Matsumoto, 2014, The Journal of Biological Chemistry.

A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif.

Y. Fujiki, W. Fan, 2006, Biochemical and biophysical research communications.

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p.

Y. Suzuki, N. Shimozawa, S. Tamura, 1998, Biochemical and biophysical research communications.

Mammalian Homologue NME3 of DYNAMO1 Regulates Peroxisome Division

H. Mandel, Y. Fujiki, T. Falik-Zaccai, 2020, International journal of molecular sciences.

Pex11mediates peroxisomal proliferation by promoting deformation of the lipid membrane

Y. Fujiki, M. Honsho, H. Niwa, 2015, Biology Open.

Mff functions with Pex11pβ and DLP1 in peroxisomal fission

A. Moser, Y. Fujiki, M. Honsho, 2013, Biology Open.

Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments.

Y. Fujiki, M. Honsho, Y. Yagita, 2008, Biochimica et biophysica acta.

Molecular cloning of Chinese hamster ceramide glucosyltransferase and its enhanced expression in peroxisome-defective mutant Z65 cells.

Y. Sakakihara, Y. Fukushima, Y. Fujiki, 2002, Archives of biochemistry and biophysics.

Distinct Modes of Ubiquitination of Peroxisome-targeting Signal Type 1 (PTS1) Receptor Pex5p Regulate PTS1 Protein Import*

K. Okumoto, Y. Fujiki, H. Noda, 2014, The Journal of Biological Chemistry.

Cysteine Ubiquitination of PTS1 Receptor Pex5p Regulates Pex5p Recycling

K. Okumoto, Y. Fujiki, Y. Matsumoto, 2011, Traffic.

The Mammalian Peroxin Pex5pL, the Longer Isoform of the Mobile Peroxisome Targeting Signal (PTS) Type 1 Transporter, Translocates the Pex7p·PTS2 Protein Complex into Peroxisomes via Its Initial Docking Site, Pex14p*

K. Ghaedi, Y. Fujiki, M. Honsho, 2000, The Journal of Biological Chemistry.

Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.

R. Wanders, R. Wanders, T. Tsukamoto, 1999, Biochemical and biophysical research communications.

Characterization of the signal peptide at the amino terminus of the rat peroxisomal 3-ketoacyl-CoA thiolase precursor.

T. Tsukamoto, M. Hijikata, T. Hashimoto, 1994, The Journal of biological chemistry.

Characterization of the Interaction between Recombinant Human Peroxin Pex3p and Pex19p

H. Kato, Yuji Kobayashi, Y. Fujiki, 2008, Journal of Biological Chemistry.

Localization of Protein Kinase NDR2 to Peroxisomes and Its Role in Ciliogenesis*

K. Okumoto, Y. Fujiki, Y. Homma, 2017, The Journal of Biological Chemistry.

Accumulation of glycolipids in mutant Chinese hamster ovary cells (Z65) with defective peroxisomal assembly and comparison of the metabolic rate of glycosphingolipids between Z65 cells and wild-type CHO-K1 cells.

A. Oka, M. Yanagisawa, N. Shimozawa, 1999, Biochimica et biophysica acta.

Transmembrane topology of the peroxin, Pex2p, an essential component for the peroxisome assembly.

Y. Fujiki, H. Otera, T. Harano, 1999, Journal of biochemistry.

Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolase.

T. Hashimoto, K. Kamijo, T. Osumi, 1989, Journal of biochemistry.

Blue Native PAGE: Applications to Study Peroxisome Biogenesis.

K. Okumoto, S. Tamura, Y. Fujiki, 2017, Methods in molecular biology.

Isolation and characterization of cDNA clones for the e1beta and E2 subunits of the branched-chain alpha-ketoacid dehydrogenase complex in Arabidopsis.

Y. Fujiki, T. Sato, A. Watanabe, 2000, The Journal of biological chemistry.

Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.

R. Wanders, Y. Suzuki, N. Shimozawa, 1999, Human molecular genetics.

The Peroxin Pex14p

K. Ghaedi, K. Okumoto, S. Tamura, 1999, The Journal of Biological Chemistry.

PEX12 encodes an integral membrane protein of peroxisomes

K. Okumoto, Y. Fujiki, 1997, Nature Genetics.

Molecular cloning and sequence of the complementary DNA encoding human mitochondrial acetoacetyl-coenzyme A thiolase and study of the variant enzymes in cultured fibroblasts from patients with 3-ketothiolase deficiency.

T. Hashimoto, T. Osumi, Y. Fujiki, 1990, The Journal of clinical investigation.

Response to darkness of late-responsive dark-inducible genes is positively regulated by leaf age and negatively regulated by calmodulin-antagonist-sensitive signalling in Arabidopsis thaliana.

S. Yoshida, Masaki Ito, Y. Fujiki, 2005, Plant & cell physiology.

Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis

T. Tsukamoto, N. Shimozawa, Y. Fujiki, 1994, Molecular and cellular biology.

Peroxisomal Targeting Signal Receptor Pex5p Interacts with Cargoes and Import Machinery Components in a Spatiotemporally Differentiated Manner: Conserved Pex5p WXXXF/Y Motifs Are Critical for Matrix Protein Import

Y. Fujiki, M. Hamasaki, H. Otera, 2002, Molecular and Cellular Biology.

Generation of Peroxisome-Deficient Somatic Animal Cell Mutants.

K. Okumoto, Y. Fujiki, 2017, Methods in molecular biology.

The Membrane Biogenesis Peroxin Pex16p

Y. Fujiki, M. Honsho, Takanobu Hiroshige, 2002, The Journal of Biological Chemistry.

A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import.

K. Ghaedi, Y. Fujiki, N. Akiyama, 2002, Biochemical and biophysical research communications.

Isolation of Chinese hamster ovary cell pex mutants: two PEX7-defective mutants.

Y. Fujiki, N. Kinoshita, Eiko Yanago, 2002, Biochemical and biophysical research communications.

Disruption of the Interaction of the Longer Isoform of Pex5p, Pex5pL, with Pex7p Abolishes Peroxisome Targeting Signal Type 2 Protein Import in Mammals

Y. Fujiki, H. Otera, T. Matsumura, 2000, The Journal of Biological Chemistry.

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

R. Wanders, R. Wanders, K. Ghaedi, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Y. Suzuki, N. Shimozawa, S. Tamura, 1998, American journal of human genetics.

The peroxisome counteracts oxidative stresses by suppressing catalase import via Pex14 phosphorylation

H. Kosako, K. Okumoto, Y. Fujiki, 2020, eLife.

Peroxisome counteracts oxidative stresses by suppressing catalase import via Pex14 phosphorylation

H. Kosako, K. Okumoto, Y. Fujiki, 2020, bioRxiv.

Shuttling Mechanism of Peroxisome Targeting Signal Type 1 Receptor Pex5: ATP-Independent Import and ATP-Dependent Export

Y. Fujiki, Non Miyata, 2005, Molecular and Cellular Biology.

Purification and Characterization, of Rice Bran Lipase II

M. Watanabe, Y. Fujiki, M. Funatsu, 1976 .

Identification of a Homozygous PEX26 Mutation in a Heimler Syndrome Patient

Young-Jae Kim, Jung‐Wook Kim, Y. Fujiki, 2021, Genes.

Isolation of intracellular membranes by means of sodium carbonate treatment: application to endoplasmic reticulum

Y. Fujiki, A. Hubbard, P. Lazarow, 1982, The Journal of cell biology.

Mild reduction of plasmalogens causes rhizomelic chondrodysplasia punctata: functional characterization of a novel mutation

Yoshiteru Sato, K. Ghaedi, Y. Fujiki, 2014, Journal of Human Genetics.

Zellwegar Syndrome: Biochemical and Morphological Studies on Two Patients Treated with Clofibrate

H. Shio, Y. Fujiki, P. Lazarow, 1985, Pediatric Research.

Biogenesis of peroxisomes.

Y. Fujiki, P. Lazarow, 1985, Annual review of cell biology.

The peroxin Pex14p is involved in LC3-dependent degradation of mammalian peroxisomes.

Y. Fujiki, S. Hara-Kuge, 2008, Experimental cell research.

Studies on the disulfide bonds in human pituitary follicle-stimulating hormone.

Y. Fujiki, P. Rathnam, B. Saxena, 1980, Biochimica et biophysica acta.

Systematic Identification of Regulators of Oxidative Stress Reveals Non-canonical Roles for Peroxisomal Import and the Pentose Phosphate Pathway.

Michael M. Dubreuil, M. Snyder, S. Dixon, 2020, Cell reports.

Studies on the unique presence of an N-acetylgalactosamine residue in the carbohydrate moieties of human follicle-stimulating hormone.

Y. Fujiki, P. Rathnam, V. P. Bhavanandan, 1982, Biochimica et biophysica acta.

Amino acid sequence of the beta-subunit of the follicle-stimulating hormone from equine pituitary glands.

Y. Fujiki, P. Rathnam, B. Saxena, 1978, The Journal of biological chemistry.

Isolation and amino acid sequence of the alpha-subunit of follicle-stimulating hormone from equine pituitary glands.

Y. Fujiki, T. Landefeld, P. Rathnam, 1978, The Journal of biological chemistry.

Alterations in the molecular species of plasmalogen phospholipids and glycolipids due to peroxisomal dysfunction in Chinese hamster ovary-mutant Z65 cells by FABMS method.

M. Mizuguchi, Y. Sakakihara, Y. Fujiki, 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

The peroxin pex3p initiates membrane assembly in peroxisome biogenesis.

K. Ghaedi, K. Okumoto, S. Tamura, 2000, Molecular biology of the cell.

Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus

K. Ohno, T. Hashimoto, S. Miyazawa, 1989, Molecular and cellular biology.

A Novel Fluorescent Sensor Protein for Visualization of Redox States in the Cytoplasm and in Peroxisomes

Yasuyoshi Sakai, S. Kuge, Y. Fujiki, 2010, Molecular and Cellular Biology.

Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.

H. Moser, A. Moser, N. Shimozawa, 2003, American journal of human genetics.

Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.

Y. Kuroki, T. Tsukamoto, Y. Suzuki, 1996, American journal of human genetics.

A human gene responsible for Zellweger syndrome that affects peroxisome assembly.

T. Tsukamoto, Y. Suzuki, N. Shimozawa, 1992, Science.

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.

T. Imanaka, T. Tsukamoto, A. Imamura, 1998, American journal of human genetics.

Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells

H. Moser, T. Hashimoto, N. Shimozawa, 1992, Human Genetics.

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 1999, Experimental cell research.

Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.

R. Wanders, R. Wanders, T. Imanaka, 1998, American journal of human genetics.

Genetic basis of peroxisomes-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts (letter)

R. Wanders, T. Imanaka, F. Beemer, 1998 .

Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.

Y. Suzuki, N. Shimozawa, K. Okumoto, 1997, Experimental cell research.

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

Y. Suzuki, N. Shimozawa, Y. Fujiki, 1992, The Journal of clinical investigation.

Topogenesis of peroxisomal proteins

T. Osumi, Y. Fujiki, 1990, BioEssays : news and reviews in molecular, cellular and developmental biology.

Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).

H. Moser, P. Watkins, Y. Fujiki, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Synthesis of 3-ketoacyl-CoA thiolase of rat liver peroxisomes on free polyribosomes as a larger precursor. Induction of thiolase mRNA activity by clofibrate.

R. Rachubinski, Y. Fujiki, P. Lazarow, 1985, The Biochemical journal.

Molecular Mechanisms of Import of Peroxisome-targeting Signal Type 2 (PTS2) Proteins by PTS2 Receptor Pex7p and PTS1 Receptor Pex5pL*

Y. Fujiki, Yukio Fujiki, S. Mukai, 2006, Journal of Biological Chemistry.

Approaches to Studies on Peroxisome Biogenesis and Human Peroxisome‐deficient Disorders

Y. Fujiki, 1996, Annals of the New York Academy of Sciences.

Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.

T Hashimoto, Y Fujiki, S Miura, 1991, Biochemical and biophysical research communications.

Molecular Basis of Mitochondrial and Peroxisomal Division Machineries

Y. Fujiki, Kie Itoh, Yuuta Imoto, 2020, International journal of molecular sciences.

Recruiting Mechanism of the AAA Peroxins, Pex1p and Pex6p, to Pex26p on the Peroxisomal Membrane

S. Tamura, Y. Fujiki, T. Matsuzaki, 2011, Traffic.

Peroxisome Biogenesis Disorders.

K. Okumoto, S. Tamura, Y. Fujiki, 2006, Advances in experimental medicine and biology.

Mutations in the Peroxin Pex26p Responsible for Peroxisome Biogenesis Disorders of Complementation Group 8 Impair Its Stability, Peroxisomal Localization, and Interaction with the Pex1p·Pex6p Complex*

Ann Moser, H. Moser, A. Moser, 2006, Journal of Biological Chemistry.

Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1

R. Wanders, T. Tsukamoto, A. Imamura, 2000, Pediatric Research.

Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans

T. Tsukamoto, A. Imamura, N. Shimozawa, 2000, Brain and Development.

Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 1999, Experimental cell research.

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.

T. Tsukamoto, A. Imamura, Y. Suzuki, 1998, Human molecular genetics.

cDNA cloning and characterization of a constitutively expressed isoform of the human peroxin Pex11p.

Y. Fujiki, I. Abe, I. Abe, 1998, Biochemical and biophysical research communications.

Newly Identified Chinese Hamster Ovary Cell Mutants Are Defective in Biogenesis of Peroxisomal Membrane Vesicles (Peroxisomal Ghosts), Representing a Novel Complementation Group in Mammals*

R. Wanders, K. Ghaedi, N. Shimozawa, 1998, The Journal of Biological Chemistry.

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.

Y. Suzuki, N. Shimozawa, K. Okumoto, 1998, Human molecular genetics.

Clofibrate‐inducible, 28‐kDa peroxisomal integral membrane protein is encoded by PEX11

K. Okumoto, S. Tamura, Y. Fujiki, 1998, FEBS letters.

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.

T. Tsukamoto, Y. Suzuki, N. Shimozawa, 1998, Proceedings of the National Academy of Sciences of the United States of America.

An Arabidopsis Homolog of Yeast ATG6/VPS30 Is Essential for Pollen Germination1[W]

K. Yoshimoto, Y. Fujiki, Y. Ohsumi, 2007, Plant Physiology.

Regulation of plasmalogen biosynthesis in mammalian cells and tissues

Y. Fujiki, M. Honsho, 2023, Brain Research Bulletin.

Multiple genes, including a member of the AAA family, are essential for degradation of unassembled subunit 2 of cytochrome c oxidase in yeast mitochondria

Y. Fujiki, T. Nakai, A. Ohashi, 1995, Molecular and cellular biology.

Dark-inducible genes from Arabidopsis thaliana are associated with leaf senescence and repressed by sugars.

Akira Watanabe, Masaki Ito, Y. Yoshikawa, 2001, Physiologia plantarum.

Plasmalogen biosynthesis is spatiotemporally regulated by sensing plasmalogens in the inner leaflet of plasma membranes

Y. Fujiki, M. Honsho, Y. Abe, 2017, Scientific Reports.

Assembly of Peroxisomal Membrane Proteins via the Direct Pex19p‐Pex3p Pathway

Y. Fujiki, Y. Yagita, Yuqiong Liu, 2016, Traffic.

Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway

Y. Fujiki, Y. Yagita, Takahide Hiromasa, 2013, The Journal of cell biology.

In Vitro Transport of Membrane Proteins to Peroxisomes by Shuttling Receptor Pex19p*

Y. Fujiki, Y. Matsuzono, Yuji Matsuzono, 2006, Journal of Biological Chemistry.

Topogenesis of Peroxisomal Membrane Protein Requires a Short, Positively Charged Intervening-loop Sequence and Flanking Hydrophobic Segments

Y. Fujiki, M. Honsho, 2001, The Journal of Biological Chemistry.

Distinct Functions of Acyl/Alkyl Dihydroxyacetonephosphate Reductase in Peroxisomes and Endoplasmic Reticulum

R. Zoeller, Y. Fujiki, M. Honsho, 2020, Frontiers in Cell and Developmental Biology.

New splicing variants of mitochondrial Rho GTPase-1 (Miro1) transport peroxisomes

K. Okumoto, Y. Fujiki, R. Toyama, 2018, The Journal of cell biology.

Peroxisome biogenesis: a novel inducible PEX19 splicing variant is involved in early stages of peroxisome proliferation

A. Matsuura, Y. Fujiki, N. Kinoshita, 2017, Journal of biochemistry.

In Vitro PMP Import Analysis Using Cell-Free Synthesized PMP and Isolated Peroxisomes.

Y. Fujiki, M. Honsho, Yuqiong Liu, 2017, Methods in molecular biology.

Peroxisomal Membrane and Matrix Protein Import Using a Semi-Intact Mammalian Cell System.

K. Okumoto, Y. Fujiki, M. Honsho, 2017, Methods in molecular biology.

Peroxisome biogenesis in mammalian cells

K. Okumoto, S. Tamura, Y. Fujiki, 2014, Front. Physiol..

System to quantify the import of peroxisomal matrix proteins by fluorescence intensity

K. Okumoto, Y. Fujiki, Masafumi Noguchi, 2013, Genes to cells : devoted to molecular & cellular mechanisms.

Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation

Y. Fujiki, T. Matsuzaki, Y. Matsuzono, 2006, Journal of Cell Science.

Intracellular Localization, Function, and Dysfunction of the Peroxisome-targeting Signal Type 2 Receptor, Pex7p, in Mammalian Cells*

K. Ghaedi, Y. Fujiki, S. Mukai, 2002, The Journal of Biological Chemistry.

Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes

T. Tsukamoto, Y. Fujiki, S. Yokota, 1990, The Journal of cell biology.

Import of a 22-kDa Peroxisomal Integral Membrane Protein into Peroxisomes in Vitro

Y. Fujiki, H. Mori, I. Kasuya, 1989 .

Import of peroxisomal membrane proteins: the interplay of Pex3p- and Pex19p-mediated interactions.

Y. Fujiki, M. Fransen, T. Matsuzaki, 2006, Biochimica et biophysica acta.

Peroxisome Biogenesis and Its Dysfunction

Y. Fujiki, 2008 .

The pathogenic peroxin Pex26p recruits the Pex1p–Pex6p AAA ATPase complexes to peroxisomes

S. Tamura, Y. Fujiki, Naomi Matsumoto, 2003, Nature Cell Biology.

Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1.

Y. Fujiki, T. Harano, S. Nose, 2001, The Biochemical journal.

Topogenesis and Homeostasis of Fatty Acyl-CoA Reductase 1*

Y. Fujiki, M. Honsho, K. Fukumoto, 2013, The Journal of Biological Chemistry.

Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes.

R. Rachubinski, Y. Fujiki, P. Lazarow, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Peroxisome biogenesis disorders: molecular basis for impaired peroxisomal membrane assembly: in metabolic functions and biogenesis of peroxisomes in health and disease.

Y. Fujiki, T. Matsuzaki, Y. Yagita, 2012, Biochimica et biophysica acta.

Peroxisome homeostasis: Mechanisms of division and selective degradation of peroxisomes in mammals.

Y. Fujiki, M. Honsho, S. Yamashita, 2016, Biochimica et biophysica acta.

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 2000, American journal of human genetics.

A Mouse Model System to Study Peroxisomal Roles in Neurodegeneration of Peroxisome Biogenesis Disorders.

S. Tamura, Y. Fujiki, M. Honsho, 2020, Advances in experimental medicine and biology.

The cytosolic peroxisome-targeting signal (PTS)-receptors, Pex7p and Pex5pL, are sufficient to transport PTS2 proteins to peroxisomes.

Y. Fujiki, T. Matsuzaki, S. Mukai, 2019, Biochimica et biophysica acta. Molecular cell research.

Peroxisome biogenesis deficiency attenuates the BDNF-TrkB pathway-mediated development of the cerebellum

K. Nakayama, T. Yamashita, Y. Fujiki, 2018, Life Science Alliance.

Identification of Peroxisomal Protein Complexes with PTS Receptors, Pex5 and Pex7, in Mammalian Cells.

K. Okumoto, Y. Fujiki, Non Miyata, 2018, Sub-cellular biochemistry.

Deficiency of a Retinal Dystrophy Protein, Acyl-CoA Binding Domain-containing 5 (ACBD5), Impairs Peroxisomal β-Oxidation of Very-long-chain Fatty Acids*

F. Alkuraya, Y. Fujiki, M. Al-Owain, 2016, The Journal of Biological Chemistry.

Fukumoto and Yukio Fujiki Masanori Honsho , Shunsuke Asaoku , Keiko Acyl-CoA Reductase 1 Topogenesis and Homeostasis of Fatty Lipids

Y. Fujiki, M. Honsho, K. Fukumoto, 2013 .

Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals.

K. Ghaedi, Y. Fujiki, M. Honsho, 2011, Journal of biochemistry.

In vitro import of peroxisome-targeting signal type 2 (PTS2) receptor Pex7p into peroxisomes.

Y. Fujiki, S. Mukai, Non Miyata, 2009, Biochimica et biophysica acta.

Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent

K. Ghaedi, Y. Fujiki, 2008, Cell biochemistry and function.

Peroxisome division is impaired in a CHO cell mutant with an inactivating point-mutation in dynamin-like protein 1 gene.

A. Tanaka, Y. Fujiki, Yukio Fujiki, 2006, Experimental cell research.

cDNA cloning and characterization of the third isoform of human peroxin Pex11p.

A. Tanaka, K. Okumoto, Y. Fujiki, 2003, Biochemical and biophysical research communications.

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6

H. Moser, A. Moser, N. Braverman, 2001, Journal of Human Genetics.

Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.

Y. Suzuki, N. Shimozawa, K. Okumoto, 1997, European journal of cell biology.

Peroxisome assembly factor–2, a putative ATPase cloned by functional complementation on a peroxisome–deficient mammalian cell mutant

T. Tsukamoto, S. Miura, N. Shimozawa, 1995, Nature Genetics.

Post-translational import of 3-ketoacyl-CoA thiolase into rat liver peroxisomes in vitro.

T. Hashimoto, S. Miyazawa, S. Miura, 1994, Journal of Biochemistry (Tokyo).

Acyl-Coa oxidase and hydratase-dehydrogenase, two enzymes of the peroxisomal beta-oxidation system, are synthesized on free polysomes of clofibrate-treated rat liver

R. Rachubinski, Y. Fujiki, P. Lazarow, 1984, The Journal of cell biology.

Origin and spatiotemporal dynamics of the peroxisomal endomembrane system

Y. Fujiki, G. Head, Baker Idi, 2014 .

Identification of beta-oxidation enzymes among peroxisomal polypeptides. Increase in Coomassie blue-stainable protein after clofibrate treatment.

T. Hashimoto, Y. Fujiki, P. Lazarow, 1982, FEBS letters.

Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells

M. Tagaya, A. Yamamoto, Y. Fujiki, 2011, Proceedings of the National Academy of Sciences.

Post-translational import of fatty acyl-CoA oxidase and catalase into peroxisomes of rat liver in vitro.

Y. Fujiki, P. Lazarow, 1985, The Journal of biological chemistry.

Plasmalogen mediates integration of adherens junction.

Y. Fujiki, M. Honsho, Y. Abe, 2019, Journal of biochemistry.

Posttranslational Regulation of Fatty Acyl-CoA Reductase 1, Far1, Controls Ether Glycerophospholipid Synthesis*♦

Y. Fujiki, M. Honsho, Shunsuke Asaoku, 2010, The Journal of Biological Chemistry.

Peroxisomes control mitochondrial dynamics and the mitochondrion-dependent apoptosis pathway

Y. Gotoh, M. Koike, Y. Fujiki, 2019, Journal of Cell Science.

Peroxisomes control mitochondrial dynamics and the mitochondrion-dependent pathway of apoptosis

Y. Gotoh, M. Koike, Y. Fujiki, 2018, bioRxiv.

Protein Import into Peroxisomes: The Principles and Methods of Studying

K. Okumoto, Y. Fujiki, M. Honsho, 2015 .

Pex5p stabilizes Pex14p: a study using a newly isolated pex5 CHO cell mutant, ZPEG101.

K. Okumoto, Y. Fujiki, Ryuichi Natsuyama, 2013, The Biochemical journal.

Pex 5 p stabilizes Pex 14 p : a study using a newly isolated pex 5 CHO cell mutant , ZPEG 101

K. Okumoto, Y. Fujiki, Ryuichi Natsuyama, 2012 .

A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.

R. Wanders, N. Shimozawa, Yasuyuki Suzuki, 2002, Biochemical and biophysical research communications.

AWP1/ZFAND6 Functions in Pex5 Export by Interacting with Cys‐Monoubiquitinated Pex5 and Pex6 AAA ATPase

K. Okumoto, Y. Fujiki, S. Mukai, 2012, Traffic.

Recent insights into peroxisome biogenesis and associated diseases

W. Chung, T. Kuroiwa, T. Yamashita, 2020, Journal of Cell Science.

Cell Death or Survival Against Oxidative Stress.

K. Okumoto, Y. Fujiki, Non Miyata, 2018, Sub-cellular biochemistry.

Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.

Y Fujiki, A. Imamura, Y. Suzuki, 2001, The Biochemical journal.

The VDAC2–BAK axis regulates peroxisomal membrane permeability

E. Cheng, K. Okumoto, Y. Fujiki, 2017, The Journal of cell biology.

Mislocalization and inhibition of acetyl-CoA carboxylase 1 by a synthetic small molecule.

Ziwei Gu, S. Wakil, L. Abu-Elheiga, 2012, The Biochemical journal.

Isolation of cDNA clones coding for peroxisomal proteins of Candida tropicalis: identification and sequence of a clone for catalase.

R. Rachubinski, Y. Fujiki, P. Lazarow, 1987, Biochimica et biophysica acta.

Biogenesis of Nonspecific Lipid Transfer Protein and Sterol Carrier Protein x

Y. Fujiki, T. Mori, H. Otera, 2001, The Journal of Biological Chemistry.

Alterations in ether lipid metabolism and the consequences for the mouse lipidome.

G. Golderer, E. Werner, G. Werner-Felmayer, 2023, Biochimica et biophysica acta. Molecular and cell biology of lipids.

A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder

Wendy K. Chung, W. Chung, Liyong Deng, 2018, Cold Spring Harbor molecular case studies.

Analysis of Plasmalogen Synthesis in Cultured Cells.

Y. Fujiki, M. Honsho, 2017, Methods in molecular biology.

Cloning of cDNA coding for peroxisomal acyl-CoA oxidase from the yeast Candida tropicalis pK233.

R. Rachubinski, Y. Fujiki, P. Lazarow, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Heating RNA before cell-free translation is essential for the efficient and reproducible synthesis of several peroxisomal proteins.

R. Rachubinski, Y. Fujiki, P. Lazarow, 1984, The Biochemical journal.

BIOGENESIS OF PEROXISOMAL PROTEINS IN VIVO AND IN VITRO *

Y. Fujiki, P. Lazarow, M. Robbi, 1982, Annals of the New York Academy of Sciences.

Molecular basis of local energy generation during mitochondrial and peroxisomal division

T. Kuroiwa, H. Kuroiwa, K. Okumoto, 2020, PLANT MORPHOLOGY.

Dynamics of the nucleoside diphosphate kinase protein DYNAMO2 correlates with the changes in the global GTP level during the cell cycle of Cyanidioschyzon merolae

T. Kuroiwa, H. Kuroiwa, K. Okumoto, 2019, Proceedings of the Japan Academy. Series B, Physical and biological sciences.

Onsite GTP fuelling via DYNAMO1 drives division of mitochondria and peroxisomes

T. Kuroiwa, H. Kuroiwa, K. Okumoto, 2018, Nature Communications.

Defining the dynamin-based ring organizing center on the peroxisome-dividing machinery isolated from Cyanidioschyzon merolae

T. Kuroiwa, H. Kuroiwa, K. Okumoto, 2017, Journal of Cell Science.

Effect of spermidine on N-formylmethionyl-tRNA binding to 30S ribosomal subunits and on N-formylmethionyl-tRNA dependent polypeptide synthesis.

Y. Fujiki, Y. Watanabe, K. Igarashi, 1978, Biochemical and biophysical research communications.

Ligand‐dependent nucleo‐cytoplasmic shuttling of peroxisome proliferator‐activated receptors, PPARα and PPARγ

Y. Fujiki, Tomoe Umemoto, 2012, Genes to cells : devoted to molecular & cellular mechanisms.

PHOSPHATIDYLSERINE SYNTHASE1 is required for microspore development in Arabidopsis thaliana.

Youngsook Lee, Y. Fujiki, M. Nishijima, 2011, The Plant journal : for cell and molecular biology.

Photoassimilation, Assimilate Translocation and Plasmodesmal Biogenesis in the Source Leaves of Arabidopsis thaliana Grown Under an Increased Atmospheric CO2 Concentration

N. Nagata, Y. Fujiki, I. Nishida, 2014, Plant & cell physiology.

Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor‐2) gene in patients with peroxisome biogenesis disorders

H. Moser, R. Wanders, G. Besley, 1999, Human mutation.

Crystal structure of the conserved N-terminal domain of the peroxisomal matrix protein import receptor, Pex14p

Jianrui Su, K. Miki, S. Tamura, 2008, Proceedings of the National Academy of Sciences.

Novel families of vacuolar amino acid transporters

Y. Fujiki, Y. Ohsumi, Y. Kakinuma, 2008, IUBMB life.

Activation of the promoters of Arabidopsis genes for the branched-chain alpha-keto acid dehydrogenase complex in transgenic tobacco BY-2 cells under sugar starvation.

Masaki Ito, Y. Fujiki, I. Nishida, 2002, Plant & cell physiology.

Nuclear transport of peroxisome-proliferator activated receptor α.

Y. Fujiki, F. Iwamoto, K. Motojima, 2011, Journal of biochemistry.

Multiple signaling pathways in gene expression during sugar starvation. Pharmacological analysis of din gene expression in suspension-cultured cells of Arabidopsis.

Y. Fujiki, I. Nishida, M. Ito, 2000, Plant physiology.

Epigenetic floral homeotic mutation in pD991-AP3-derived T-DNA-tagged lines for CTP:Phosphorylcholine cytidylyltransferase (CCT) Genes: The homeotic mutation of the cct1-1 allele is enhanced by the cct2 allele and alleviated by CCT1 overexpression

Y. Fujiki, Yasuyo Yamaoka, I. Nishida, 2015, Journal of Plant Biology.

Induction, identification, and cell-free translation of mRNAs coding for peroxisomal proteins in Candida tropicalis.

R. Rachubinski, Y. Fujiki, P. Lazarow, 1986, The Journal of biological chemistry.

Genetic defects in peroxisome morphogenesis (Pex11β, DLP1 , and NME3 ) affect DHA ‐phospholipid metabolism

H. Waterham, H. Mandel, R. Wanders, 2022, Journal of Inherited Metabolic Disease.

Enzymatic Properties of Rice Bran Lipase

Y. Fujiki, M. Sugano, M. Funatsu, 1973 .

Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.

R. Wanders, A. Imamura, Y. Suzuki, 2000, Biochemical and biophysical research communications.

A novel mutation, R125X in peroxisome assembly factor‐1 responsible for zellweger syndrome

T. Tsukamoto, N. Shimozawa, Yasuyuki Suzuki, 1998, Human mutation.

A New Paradigm in Catalase Research.

M. Bassik, Y. Fujiki, 2021, Trends in cell biology.

Correction by Gene Expression of Biochemical Abnormalities in Fibroblasts from Zellweger Patients

T. Tsukamoto, T. Hashimoto, K. Kamijo, 1996, Pediatric Research.

Biogenesis of Peroxisomes in Rat Liver and Candida Tropicalis

H. Shio, R. Rachubinski, Y. Fujiki, 1987 .

Genetic defects in peroxisome morphogenesis (Pex11β, dynamin‐like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid‐phospholipid metabolism

H. Waterham, H. Mandel, R. Wanders, 2022, Journal of inherited metabolic disease.

Asymmetric Distribution of Plasmalogens and Their Roles—A Mini Review

Y. Fujiki, M. Honsho, 2023, Membranes.