FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Kanji Okumoto

Research Profile

Anatomy

Living Beings

Chemicals & Drugs

Disorders

Physiology

Procedures

Genes & Molecular Sequences

Amino Acid Sequences

Concepts & Ideas

Co-author Network

Publications

TOP 3
Ryuichi Natsuyama; Kanji Okumoto; Yukio Fujiki
Pex5p stabilizes Pex14p: a study using a newly isolated pex5 CHO cell mutant, ZPEG101.
Kanji Okumoto; Yui Matsumoto; Sachi Misono; Non Miyata; Satoru Mukai; Yukio Fujiki
Cysteine ubiquitination of PTS1 receptor Pex5p regulates Pex5p recycling.
Yukio Fujiki; Kanji Okumoto; Naohiko Kinoshita; Kamran Ghaedi
Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Kanji Okumoto (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Ryuichi Natsuyama; Kanji Okumoto; Yukio Fujiki
Pex5p stabilizes Pex14p: a study using a newly isolated pex5 CHO cell mutant, ZPEG101.
The Biochemical journal 2013;449(1):195-207.
2011: Kanji Okumoto; Yui Matsumoto; Sachi Misono; Non Miyata; Satoru Mukai; Yukio Fujiki
Cysteine ubiquitination of PTS1 receptor Pex5p regulates Pex5p recycling.
Traffic (Copenhagen, Denmark) 2011;12(8):1067-83.
2006: Yukio Fujiki; Kanji Okumoto; Naohiko Kinoshita; Kamran Ghaedi
Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants.
Biochimica et biophysica acta 2006;1763(12):1374-81.
2003: Atsushi Tanaka; Kanji Okumoto; Yukio Fujiki
cDNA cloning and characterization of the third isoform of human peroxin Pex11p.
Biochemical and biophysical research communications 2003;300(4):819-23.
2000: Kanji Okumoto; I Abe; Yukio Fujiki
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: Kamran Ghaedi; Shigehiko Tamura; Kanji Okumoto; Yuji Matsuzono; Yukio Fujiki
The peroxin pex3p initiates membrane assembly in peroxisome biogenesis.
Molecular biology of the cell 2000;11(6):2085-102.
2000: Yukio Fujiki; Kanji Okumoto
[Peroxisome biogenesis and human disorders].
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 2000;45(5):691-9.
2000: Yukio Fujiki; Kanji Okumoto; HIDENORI OTERA; Shigehiko Tamura
Peroxisome biogenesis and molecular defects in peroxisome assembly disorders.
Cell biochemistry and biophysics 2000;32 Spring():155-64.
1999: Kamran Ghaedi; A Kawai; Kanji Okumoto; Shigehiko Tamura; Nobuyuki Shimozawa; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
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: Nobuhiro Shimizu; Ryota Itoh; Y Hirono; HIDENORI OTERA; Kamran Ghaedi; K Tateishi; Shigehiko Tamura; Kanji Okumoto; T Harano; Satoru Mukai; Yukio Fujiki
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.
1998: Naohiko Kinoshita; Kamran Ghaedi; Nobuyuki Shimozawa; Ronald J A Wanders; Yuji Matsuzono; T Imanaka; Kanji Okumoto; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
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: Kanji Okumoto; Ryota Itoh; Nobuyuki Shimozawa; Yasuyuki Suzuki; Shigehiko Tamura; Naomi Kondo; Yukio Fujiki
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
Human molecular genetics 1998;7(9):1399-405.
1998: I Abe; Kanji Okumoto; Shigehiko Tamura; Yukio Fujiki
Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11.
FEBS letters 1998;431(3):468-72.
1998: Kanji Okumoto; Nobuyuki Shimozawa; A Kawai; Shigehiko Tamura; Toshiro Tsukamoto; Takashi Osumi; H Moser; Ronald J A Wanders; Yasuyuki Suzuki; Naomi Kondo; Yukio Fujiki
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: Shigehiko Tamura; Kanji Okumoto; R Toyama; Nobuyuki Shimozawa; Toshiro Tsukamoto; Yasuyuki Suzuki; Takashi Osumi; Naomi Kondo; Yukio Fujiki
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: Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; A Imamura; Toshiro Tsukamoto; Takashi Osumi; K Tateishi; Kanji Okumoto; Yukio Fujiki; Tadao Orii; PG Barth; Ronald J A Wanders; Naomi Kondo
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: HIDENORI OTERA; Kanji Okumoto; K Tateishi; Y Ikoma; E Matsuda; M Nishimura; Toshiro Tsukamoto; Takashi Osumi; K Ohashi; O Higuchi; Yukio Fujiki
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.
1997: K Tateishi; Kanji Okumoto; Nobuyuki Shimozawa; Toshiro Tsukamoto; Takashi Osumi; Yasuyuki Suzuki; Naomi Kondo; I Okano; Yukio Fujiki
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: Kanji Okumoto; A Bogaki; K Tateishi; Toshiro Tsukamoto; Takashi Osumi; Nobuyuki Shimozawa; Yasuyuki Suzuki; Tadao Orii; Yukio Fujiki
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: Toshiro Tsukamoto; A Bogaki; Kanji Okumoto; K Tateishi; Yukio Fujiki; Nobuyuki Shimozawa; Y Suzuki; N Kondo; Takashi Osumi
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.