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

Por Okumoto, Kanji, Kametani, Yukari, Fujiki, Yukio
Publicado em 2011

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

Por Okumoto, Kanji, Noda, Hiromi, Fujiki, Yukio
Publicado em 2014

The Peroxin Pex3p Initiates Membrane Assembly in Peroxisome Biogenesis

Por Ghaedi, Kamran, Tamura, Shigehiko, Okumoto, Kanji, Matsuzono, Yuji, Fujiki, Yukio
Publicado em 2000

Peroxisome biogenesis in mammalian cells

Por Fujiki, Yukio, Okumoto, Kanji, Mukai, Satoru, Honsho, Masanori, Tamura, Shigehiko
Publicado em 2014

BAK regulates catalase release from peroxisomes

Por Fujiki, Yukio, Miyata, Non, Mukai, Satoru, Okumoto, Kanji, Cheng, Emily H.
Publicado no Mol Cell Oncol (2017)

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

Por Okumoto, Kanji, Ono, Tatsuaki, Toyama, Ryusuke, Shimomura, Ayako, Nagata, Aiko, Fujiki, Yukio
Publicado no J Cell Biol (2018)

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

Por Abe, Shoko, Nagai, Tomoaki, Masukawa, Moe, Okumoto, Kanji, Homma, Yuta, Fujiki, Yukio, Mizuno, Kensaku
Publicado no J Biol Chem (2017)

The VDAC2–BAK axis regulates peroxisomal membrane permeability

Por Hosoi, Ken-ichiro, Miyata, Non, Mukai, Satoru, Furuki, Satomi, Okumoto, Kanji, Cheng, Emily H., Fujiki, Yukio
Publicado no J Cell Biol (2017)

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

Por Tamura, Shigehiko, Okumoto, Kanji, Toyama, Ryusuke, Shimozawa, Nobuyuki, Tsukamoto, Toshiro, Suzuki, Yasuyuki, Osumi, Takashi, Kondo, Naomi, Fujiki, Yukio
Publicado em 1998

Peroxisome Targeting Signal Type 1 (PTS1) Receptor Is Involved in Import of Both PTS1 and PTS2: Studies with PEX5-Defective CHO Cell Mutants

Por Otera, Hidenori, Okumoto, Kanji, Tateishi, Keita, Ikoma, Yuka, Matsuda, Eiko, Nishimura, Maki, Tsukamoto, Toshiro, Osumi, Takashi, Ohashi, Kazumasa, Higuchi, Osamu, Fujiki, Yukio
Publicado em 1998

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

Por Okumoto, Kanji, Shimozawa, Nobuyuki, Kawai, Atsusi, Tamura, Shigehiko, Tsukamoto, Toshiro, Osumi, Takashi, Moser, Hugo, Wanders, Ronald J. A., Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Publicado em 1998