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Shigehiko Tamura

Showing results (11-20 of 23) with videos related to

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Biochimica Et Biophysica Acta|November 15, 2011
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 biogenesisYukio Fujiki, Chika Nashiro, Non Miyata, et al.
Traffic (Copenhagen, Denmark)|March 3, 2011
Recruiting mechanism of the AAA peroxins, Pex1p and Pex6p, to Pex26p on the peroxisomal membraneChika Nashiro, Astuko Kashiwagi, Takashi Matsuzaki, et al.
Frontiers in Physiology|September 2, 2014
Peroxisome biogenesis in mammalian cellsYukio Fujiki, Kanji Okumoto, Satoru Mukai, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2009
Crystal structure of the conserved N-terminal domain of the peroxisomal matrix protein import receptor, Pex14pJian-Rong Su, Kazuki Takeda, Shigehiko Tamura, et al.
Biochemical and Biophysical Research Communications|March 3, 2010
Monomer-dimer transition of the conserved N-terminal domain of the mammalian peroxisomal matrix protein import receptor, Pex14pJian-Rong Su, Kazuki Takeda, Shigehiko Tamura, et al.
The Journal of Cell Biology|August 28, 2020
Mitotic phosphorylation of Pex14p regulates peroxisomal import machineryKoichiro Yamashita, Shigehiko Tamura, Masanori Honsho, et al.
The Journal of Biological Chemistry|November 1, 2005
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 complexSatomi Furuki, Shigehiko Tamura, Naomi Matsumoto, et al.
Frontiers in Cell and Developmental Biology|November 9, 2020
Peroxisome Deficiency Impairs BDNF Signaling and MemoryYuichi Abe, Yoshiki Nishimura, Kaori Nakamura, et al.
Cold Spring Harbor Molecular Case Studies|November 18, 2018
A newly identified mutation in the <i>PEX26</i> gene is associated with a milder form of Zellweger spectrum disorderAkemi J Tanaka, Kanji Okumoto, Shigehiko Tamura, et al.
Journal of Developmental Biology|June 25, 2025
Ribosome Incorporation Transdifferentiates Chick Primary Cells and Induces Their Proliferation by Secreting Growth FactorsShota Inoue, Arif Istiaq, Anamika Datta, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Biochimica Et Biophysica Acta|November 15, 2011
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 biogenesisYukio Fujiki, Chika Nashiro, Non Miyata, et al.
Traffic (Copenhagen, Denmark)|March 3, 2011
Recruiting mechanism of the AAA peroxins, Pex1p and Pex6p, to Pex26p on the peroxisomal membraneChika Nashiro, Astuko Kashiwagi, Takashi Matsuzaki, et al.
Frontiers in Physiology|September 2, 2014
Peroxisome biogenesis in mammalian cellsYukio Fujiki, Kanji Okumoto, Satoru Mukai, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 6, 2009
Crystal structure of the conserved N-terminal domain of the peroxisomal matrix protein import receptor, Pex14pJian-Rong Su, Kazuki Takeda, Shigehiko Tamura, et al.
Biochemical and Biophysical Research Communications|March 3, 2010
Monomer-dimer transition of the conserved N-terminal domain of the mammalian peroxisomal matrix protein import receptor, Pex14pJian-Rong Su, Kazuki Takeda, Shigehiko Tamura, et al.
The Journal of Cell Biology|August 28, 2020
Mitotic phosphorylation of Pex14p regulates peroxisomal import machineryKoichiro Yamashita, Shigehiko Tamura, Masanori Honsho, et al.
The Journal of Biological Chemistry|November 1, 2005
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 complexSatomi Furuki, Shigehiko Tamura, Naomi Matsumoto, et al.
Frontiers in Cell and Developmental Biology|November 9, 2020
Peroxisome Deficiency Impairs BDNF Signaling and MemoryYuichi Abe, Yoshiki Nishimura, Kaori Nakamura, et al.
Cold Spring Harbor Molecular Case Studies|November 18, 2018
A newly identified mutation in the <i>PEX26</i> gene is associated with a milder form of Zellweger spectrum disorderAkemi J Tanaka, Kanji Okumoto, Shigehiko Tamura, et al.
Journal of Developmental Biology|June 25, 2025
Ribosome Incorporation Transdifferentiates Chick Primary Cells and Induces Their Proliferation by Secreting Growth FactorsShota Inoue, Arif Istiaq, Anamika Datta, et al.
Pageof 3