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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 biogenesis
Yukio 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 membrane
Chika Nashiro, Astuko Kashiwagi, Takashi Matsuzaki, et al.
Frontiers in Physiology
|
September 2, 2014
Peroxisome biogenesis in mammalian cells
Yukio 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, Pex14p
Jian-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, Pex14p
Jian-Rong Su, Kazuki Takeda, Shigehiko Tamura, et al.
The Journal of Cell Biology
|
August 28, 2020
Mitotic phosphorylation of Pex14p regulates peroxisomal import machinery
Koichiro 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 complex
Satomi Furuki, Shigehiko Tamura, Naomi Matsumoto, et al.
Frontiers in Cell and Developmental Biology
|
November 9, 2020
Peroxisome Deficiency Impairs BDNF Signaling and Memory
Yuichi 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 disorder
Akemi 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 Factors
Shota Inoue, Arif Istiaq, Anamika Datta, et al.
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Search research articles
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Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 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 biogenesis
Yukio 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 membrane
Chika Nashiro, Astuko Kashiwagi, Takashi Matsuzaki, et al.
Frontiers in Physiology
|
September 2, 2014
Peroxisome biogenesis in mammalian cells
Yukio 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, Pex14p
Jian-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, Pex14p
Jian-Rong Su, Kazuki Takeda, Shigehiko Tamura, et al.
The Journal of Cell Biology
|
August 28, 2020
Mitotic phosphorylation of Pex14p regulates peroxisomal import machinery
Koichiro 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 complex
Satomi Furuki, Shigehiko Tamura, Naomi Matsumoto, et al.
Frontiers in Cell and Developmental Biology
|
November 9, 2020
Peroxisome Deficiency Impairs BDNF Signaling and Memory
Yuichi 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 disorder
Akemi 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 Factors
Shota Inoue, Arif Istiaq, Anamika Datta, et al.
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