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Yukio Fujiki

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Co-Publications
Name
36
Shimozawa, Nobuyuki
35
Suzuki, Yasuyuki
30
Kondo, Naomi
24
Osumi, Takashi
20
Tamura, Shigehiko
18
Okumoto, Kanji
17
Tsukamoto, Toshiro
16
Orii, Tadao
12
Ghaedi, Kamran
12
Wanders, Ronald
11
Zhang, Zhongyi
10
Imamura, A
8
Otera, Hidenori
7
Mukai, Satoru
7
Matsumoto, Naomi

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Publications

TOP 3
Miyata Non; Hosoi Ken-ichiro; Mukai Satoru; Fujiki Yukio
In vitro import of peroxisome-targeting signal type 2 (PTS2) receptor Pex7p into peroxisomes.
Su Jian-Rong; Takeda Kazuki; Tamura Shigehiko; Fujiki Yukio; Miki Kunio
Crystal structure of the conserved N-terminal domain of the peroxisomal matrix protein import receptor, Pex14p.
Matsuzaki Takashi; Fujiki Yukio
The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway.

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All Publications

2009: Miyata Non; Hosoi Ken-ichiro; Mukai Satoru; Fujiki Yukio
In vitro import of peroxisome-targeting signal type 2 (PTS2) receptor Pex7p into peroxisomes.
Biochimica et biophysica acta 2009;1793(5):860-70.
2009: Su Jian-Rong; Takeda Kazuki; Tamura Shigehiko; Fujiki Yukio; Miki Kunio
Crystal structure of the conserved N-terminal domain of the peroxisomal matrix protein import receptor, Pex14p.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(2):417-21.
2008: Matsuzaki Takashi; Fujiki Yukio
The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway.
The Journal of cell biology 2008;183(7):1275-86.
2008: Hara-Kuge Sayuri; Fujiki Yukio
The peroxin Pex14p is involved in LC3-dependent degradation of mammalian peroxisomes.
Experimental cell research 2008;314(19):3531-41.
2008: Honsho Masanori; Yagita Yuichi; Kinoshita Naohiko; Fujiki Yukio
Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments.
Biochimica et biophysica acta 2008;1783(10):1857-65.
2008: Ghaedi Kamran; Fujiki Yukio
Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent.
Cell biochemistry and function 2008;26(6):684-91.
2008: Sato Yasuhiko; Shibata Hiroyuki; Nakano Hiroaki; Matsuzono Yuji; Kashiwayama Yoshinori; Kobayashi Yuji; Fujiki Yukio; Imanaka Tsuneo; Kato Hiroaki
Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction.
The Journal of biological chemistry 2008;283(10):6136-44.
2008: Fujiki Yukio; Miyata Non; Matsumoto Naomi; Tamura Shigehiko
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.
Biochemical Society transactions 2008;36(Pt 1):109-13.
2007: Kobayashi Shinta; Tanaka Atsushi; Fujiki Yukio
Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis.
Experimental cell research 2007;313(8):1675-86.
2006: Fujiki Yukio; Matsuzono Yuji; Matsuzaki Takashi; Fransen Marc
Import of peroxisomal membrane proteins: the interplay of Pex3p- and Pex19p-mediated interactions.
Biochimica et biophysica acta 2006;1763(12):1639-46.
2006: Fujiki Yukio; Okumoto Kanji; Kinoshita Naohiko; Ghaedi Kamran
Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants.
Biochimica et biophysica acta 2006;1763(12):1374-81.
2006: Mukai Satoru; Fujiki Yukio
Molecular mechanisms of import of peroxisome-targeting signal type 2 (PTS2) proteins by PTS2 receptor Pex7p and PTS1 receptor Pex5pL.
The Journal of biological chemistry 2006;281(49):37311-20.
2006: Matsuzono Yuji; Matsuzaki Takashi; Fujiki Yukio
Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation.
Journal of cell science 2006;119(Pt 17):3539-50.
2006: Tamura Shigehiko; Yasutake Shinobu; Matsumoto Naomi; Fujiki Yukio
Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p.
The Journal of biological chemistry 2006;281(38):27693-704.
2006: Fan Wei; Fujiki Yukio
A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif.
Biochemical and biophysical research communications 2006;345(4):1434-9.
2006: Tanaka Atsushi; Kobayashi Shinta; Fujiki Yukio
Peroxisome division is impaired in a CHO cell mutant with an inactivating point-mutation in dynamin-like protein 1 gene.
Experimental cell research 2006;312(9):1671-84.
2006: Itoh Ryota; Fujiki Yukio
Functional domains and dynamic assembly of the peroxin Pex14p, the entry site of matrix proteins.
The Journal of biological chemistry 2006;281(15):10196-205.
2006: Matsuzono Yuji; Fujiki Yukio
In vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19p.
The Journal of biological chemistry 2006;281(1):36-42.
2006: Furuki Satomi; Tamura Shigehiko; Matsumoto Naomi; Miyata Non; Moser Ann; Moser Hugo W; Fujiki Yukio
Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex.
The Journal of biological chemistry 2006;281(3):1317-23.
2005: Miyata Non; Fujiki Yukio
Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export.
Molecular and cellular biology 2005;25(24):10822-32.
2003: Matsumoto Naomi; Tamura Shigehiko; Furuki Satomi; Miyata Non; Moser Ann; Shimozawa Nobuyuki; Moser Hugo W; Suzuki Yasuyuki; Kondo Naomi; Fujiki Yukio
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
American journal of human genetics 2003;73(2):233-46.
2003: Fujiki Yukio
[Peroxisome biogenesis and human disorders]
Seikagaku. The Journal of Japanese Biochemical Society 2003;75(6):459-64.
2003: Matsumoto Naomi; Tamura Shigehiko; Fujiki Yukio
The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes.
Nature cell biology 2003;5(5):454-60.
2003: Tanaka Atsushi; Okumoto Kanji; Fujiki Yukio
cDNA cloning and characterization of the third isoform of human peroxin Pex11p.
Biochemical and biophysical research communications 2003;300(4):819-23.
2002: Honsho Masanori; Hiroshige Takanobu; Fujiki Yukio
The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.
The Journal of biological chemistry 2002;277(46):44513-24.
2002: Akiyama Noriko; Ghaedi Kamran; Fujiki Yukio
A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import.
Biochemical and biophysical research communications 2002;293(5):1523-9.
2002: Yanago Eiko; Hiromasa Takahide; Matsumura Tsuyoshi; Kinoshita Naohiko; Fujiki Yukio
Isolation of Chinese hamster ovary cell pex mutants: two PEX7-defective mutants.
Biochemical and biophysical research communications 2002;293(1):225-30.
2002: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Suzuki Yasuyuki; Fujiki Yukio; Wanders Ronald J A; Kondo Naomi
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.
Biochemical and biophysical research communications 2002;292(1):109-12.
2002: Otera Hidenori; Setoguchi Kiyoko; Hamasaki Maho; Kumashiro Toshitaka; Shimizu Nobuhiro; Fujiki Yukio
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.
Molecular and cellular biology 2002;22(6):1639-55.
2002: Mukai Satoru; Ghaedi Kamran; Fujiki Yukio
Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells.
The Journal of biological chemistry 2002;277(11):9548-61.
2001: Suzuki Y; Shimozawa N; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Kondo N
Genetic and molecular bases of peroxisome biogenesis disorders.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(5):372-6.
2001: Tamura S; Matsumoto N; Imamura A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
The Biochemical journal 2001;357(Pt 2):417-26.
2001: Harano T; Nose S; Uezu R; Shimizu N; Fujiki Y
Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1.
The Biochemical journal 2001;357(Pt 1):157-65.
2001: Honsho M; Fujiki Y
Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34.
The Journal of biological chemistry 2001;276(12):9375-82.
2001: Otera H; Nishimura M; Setoguchi K; Mori T; Fujiki Y
Biogenesis of nonspecific lipid transfer protein and sterol carrier protein x: studies using peroxisome assembly-defective pex cell mutants.
The Journal of biological chemistry 2001;276(4):2858-64.
2001: Matsumoto N; Tamura S; Moser A; Moser H W; Braverman N; Suzuki Y; Shimozawa N; Kondo N; Fujiki Y
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.
Journal of human genetics 2001;46(5):273-7.
2000: Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Wanders R J; Kondo N
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.
Pediatric research 2000;48(4):541-5.
2000: Ghaedi K; Honsho M; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
American journal of human genetics 2000;67(4):976-81.
2000: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Ghaedi K; Fujiki Y; Kondo N
Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.
Human molecular genetics 2000;9(13):1995-9.
2000: Okumoto K; Abe I; Fujiki Y
Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p.
The Journal of biological chemistry 2000;275(33):25700-10.
2000: Matsumura T; Otera H; Fujiki Y
Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. Study with a novel Pex5-impaired Chinese hamster ovary cell mutant.
The Journal of biological chemistry 2000;275(28):21715-21.
2000: Otera H; Harano T; Honsho M; Ghaedi K; Mukai S; Tanaka A; Kawai A; Shimizu N; Fujiki Y
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.
The Journal of biological chemistry 2000;275(28):21703-14.
2000: Fujiki Y
Peroxisome biogenesis and peroxisome biogenesis disorders.
FEBS letters 2000;476(1-2):42-6.
2000: Ghaedi K; Tamura S; Okumoto K; Matsuzono Y; Fujiki Y
The peroxin pex3p initiates membrane assembly in peroxisome biogenesis.
Molecular biology of the cell 2000;11(6):2085-102.
2000: Fujiki Y; Okumoto K
[Peroxisome biogenesis and human disorders]
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 2000;45(5):691-9.
2000: Shimozawa N; Zhang Z; Imamura A; Suzuki Y; Fujiki Y; Tsukamoto T; Osumi T; Aubourg P; Wanders R J; Kondo N
Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.
Biochemical and biophysical research communications 2000;268(1):31-5.
2000: Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Kondo N
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.
Brain & development 2000;22(1):8-12.
2000: Fujiki Y; Okumoto K; Otera H; Tamura S
Peroxisome biogenesis and molecular defects in peroxisome assembly disorders.
Cell biochemistry and biophysics 2000;32 Spring():155-64.
1999: Shimozawa N; Imamura A; Zhang Z; Suzuki Y; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Wanders R J; Besley G; Kondo N
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.
Journal of medical genetics 1999;36(10):779-81.
1999: Toyama R; Mukai S; Itagaki A; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Wanders R J; Fujiki Y
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.
Human molecular genetics 1999;8(9):1673-81.
1999: Shimozawa N; Zhang Z; Suzuki Y; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Barth P G; Wanders R J; Kondo N
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.
Biochemical and biophysical research communications 1999;262(2):504-8.
1999: Harano T; Shimizu N; Otera H; Fujiki Y
Transmembrane topology of the peroxin, Pex2p, an essential component for the peroxisome assembly.
Journal of biochemistry 1999;125(6):1168-74.
1999: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Toyama R; Mukai S; Fujiki Y; Tsukamoto T; Osumi T; Orii T; Wanders R J; Kondo N
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
Human molecular genetics 1999;8(6):1077-83.
1999: Ghaedi K; Kawai A; Okumoto K; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.
Experimental cell research 1999;248(2):489-97.
1999: Ghaedi K; Itagaki A; Toyama R; Tamura S; Matsumura T; Kawai A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
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.
Experimental cell research 1999;248(2):482-8.
1999: Shimizu N; Itoh R; Hirono Y; Otera H; Ghaedi K; Tateishi K; Tamura S; Okumoto K; Harano T; Mukai S; Fujiki Y
The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis.
The Journal of biological chemistry 1999;274(18):12593-604.
1999: Matsuzono Y; Kinoshita N; Tamura S; Shimozawa N; Hamasaki M; Ghaedi K; Wanders R J; Suzuki Y; Kondo N; Fujiki Y
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(5):2116-21.
1999: Zhang Z; Suzuki Y; Shimozawa N; Fukuda S; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Wanders R J; Barth P G; Moser H W; Paton B C; Besley G T; Kondo N
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.
Human mutation 1999;13(6):487-96.
1998: Honsho M; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
American journal of human genetics 1998;63(6):1622-30.
1998: Imamura A; Tamura S; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Orii T; Kondo N; Osumi T; Fujiki Y
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.
Human molecular genetics 1998;7(13):2089-94.
1998: Abe I; Fujiki Y
cDNA cloning and characterization of a constitutively expressed isoform of the human peroxin Pex11p.
Biochemical and biophysical research communications 1998;252(2):529-33.
1998: Kinoshita N; Ghaedi K; Shimozawa N; Wanders R J; Matsuzono Y; Imanaka T; Okumoto K; Suzuki Y; Kondo N; Fujiki Y
Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.
The Journal of biological chemistry 1998;273(37):24122-30.
1998: Okumoto K; Itoh R; Shimozawa N; Suzuki Y; Tamura S; Kondo N; Fujiki Y
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
Human molecular genetics 1998;7(9):1399-405.
1998: Abe I; Okumoto K; Tamura S; Fujiki Y
Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11.
FEBS letters 1998;431(3):468-72.
1998: Okumoto K; Shimozawa N; Kawai A; Tamura S; Tsukamoto T; Osumi T; Moser H; Wanders R J; Suzuki Y; Kondo N; Fujiki Y
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.
Molecular and cellular biology 1998;18(7):4324-36.
1998: Tamura S; Shimozawa N; Suzuki Y; Tsukamoto T; Osumi T; Fujiki Y
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p.
Biochemical and biophysical research communications 1998;245(3):883-6.
1998: Tamura S; Okumoto K; Toyama R; Shimozawa N; Tsukamoto T; Suzuki Y; Osumi T; Kondo N; Fujiki Y
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(8):4350-5.
1998: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Tsukamoto T; Osumi T; Tateishi K; Okumoto K; Fujiki Y; Orii T; Barth P G; Wanders R J; Kondo N
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.
Biochemical and biophysical research communications 1998;243(2):368-71.
1998: Otera H; Okumoto K; Tateishi K; Ikoma Y; Matsuda E; Nishimura M; Tsukamoto T; Osumi T; Ohashi K; Higuchi O; Fujiki Y
Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.
Molecular and cellular biology 1998;18(1):388-99.
1998: Shimozawa N; Suzuki Y; Tomatsu S; Nakamura H; Kono T; Takada H; Tsukamoto T; Fujiki Y; Orii T; Kondo N
A novel mutation, R125X in peroxisome assembly factor-1 responsible for Zellweger syndrome.
Human mutation 1998;Suppl 1():S134-6.
1997: Fujiki Y
Molecular defects in genetic diseases of peroxisomes.
Biochimica et biophysica acta 1997;1361(3):235-50.
1997: Tateishi K; Okumoto K; Shimozawa N; Tsukamoto T; Osumi T; Suzuki Y; Kondo N; Okano I; Fujiki Y
Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.
European journal of cell biology 1997;73(4):352-9.
1997: Okumoto K; Bogaki A; Tateishi K; Tsukamoto T; Osumi T; Shimozawa N; Suzuki Y; Orii T; Fujiki Y
Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.
Experimental cell research 1997;233(1):11-20.
1997: Tsukamoto T; Bogaki A; Okumoto K; Tateishi K; Fujiki Y; Shimozawa N; Suzuki Y; Kondo N; Osumi T
Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor.
Biochemical and biophysical research communications 1997;230(2):402-6.
1996: Fujiki Y
Approaches to studies on peroxisome biogenesis and human peroxisome-deficient disorders.
Annals of the New York Academy of Sciences 1996;804():491-501.
1996: Fukuda S; Shimozawa N; Suzuki Y; Zhang Z; Tomatsu S; Tsukamoto T; Hashiguchi N; Osumi T; Masuno M; Imaizumi K; Kuroki Y; Fujiki Y; Orii T; Kondo N
Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.
American journal of human genetics 1996;59(6):1210-20.
1996: Shimozawa N; Suzuki Y; Tomatsu S; Tsukamoto T; Osumi T; Fujiki Y; Kamijo K; Hashimoto T; Kondo N; Orii T
Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
Pediatric research 1996;39(5):812-5.
1995: Tsukamoto T; Miura S; Nakai T; Yokota S; Shimozawa N; Suzuki Y; Orii T; Fujiki Y; Sakai F; Bogaki A; Yasumo H; Osumi T
Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant.
Nature genetics 1995;11(4):395-401.
1995: Fujiki Y
[Biogenesis of peroxisomes and human peroxisomal disorders]
Seikagaku. The Journal of Japanese Biochemical Society 1995;67(3):204-23.
1994: Fujiki Y
[Human peroxisome-deficient disorders and pathogenic gene]
Rinsho shinkeigaku = Clinical neurology 1994;34(12):1219-21.
1994: Masuno M; Shimozawa N; Suzuki Y; Kondo N; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Imaizumi K; Kuroki Y
Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization.
Genomics 1994;20(1):141-2.
1994: Tsukamoto T; Hata S; Yokota S; Miura S; Fujiki Y; Hijikata M; Miyazawa S; Hashimoto T; Osumi T
Characterization of the signal peptide at the amino terminus of the rat peroxisomal 3-ketoacyl-CoA thiolase precursor.
The Journal of biological chemistry 1994;269(8):6001-10.
1992: Yajima S; Suzuki Y; Shimozawa N; Yamaguchi S; Orii T; Fujiki Y; Osumi T; Hashimoto T; Moser H W
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.
Human genetics 1992;88(5):491-9.
1992: Shimozawa N; Tsukamoto T; Suzuki Y; Orii T; Shirayoshi Y; Mori T; Fujiki Y
A human gene responsible for Zellweger syndrome that affects peroxisome assembly.
Science (New York, N.Y.) 1992;255(5048):1132-4.
1991: Osumi T; Tsukamoto T; Hata S; Yokota S; Miura S; Fujiki Y; Hijikata M; Miyazawa S; Hashimoto T
Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.
Biochemical and biophysical research communications 1991;181(3):947-54.

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