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

Autor Tamura, Shigehiko, Matsumoto, Naomi, Takeba, Ryota, Fujiki, Yukio
Vydáno 2014

The Peroxin Pex3p Initiates Membrane Assembly in Peroxisome Biogenesis

Autor Ghaedi, Kamran, Tamura, Shigehiko, Okumoto, Kanji, Matsuzono, Yuji, Fujiki, Yukio
Vydáno 2000

Peroxisome biogenesis in mammalian cells

Autor Fujiki, Yukio, Okumoto, Kanji, Mukai, Satoru, Honsho, Masanori, Tamura, Shigehiko
Vydáno 2014

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

Autor Su, Jian-Rong, Takeda, Kazuki, Tamura, Shigehiko, Fujiki, Yukio, Miki, Kunio
Vydáno 2009

Mitotic phosphorylation of Pex14p regulates peroxisomal import machinery

Autor Yamashita, Koichiro, Tamura, Shigehiko, Honsho, Masanori, Yada, Hiroto, Yagita, Yuichi, Kosako, Hidetaka, Fujiki, Yukio
Vydáno v J Cell Biol (2020)

Peroxisome Deficiency Impairs BDNF Signaling and Memory

Autor Abe, Yuichi, Nishimura, Yoshiki, Nakamura, Kaori, Tamura, Shigehiko, Honsho, Masanori, Udo, Hiroshi, Yamashita, Toshihide, Fujiki, Yukio
Vydáno v Front Cell Dev Biol (2020)

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

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

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

Autor Tanaka, Akemi J., Okumoto, Kanji, Tamura, Shigehiko, Abe, Yuichi, Hirsch, Yoel, Deng, Liyong, Ekstein, Joseph, Chung, Wendy K., Fujiki, Yukio
Vydáno v Cold Spring Harb Mol Case Stud (2019)

Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation

Autor Matsumoto, Naomi, Tamura, Shigehiko, Furuki, Satomi, Miyata, Non, Moser, Ann, Shimozawa, Nobuyuki, Moser, Hugo W., Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Vydáno 2003

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

Autor Matsuzono, Yuji, Kinoshita, Naohiko, Tamura, Shigehiko, Shimozawa, Nobuyuki, Hamasaki, Maho, Ghaedi, Kamran, Wanders, Ronald J. A., Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Vydáno 1999

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

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