Shigehiko Tamura

The pathogenic peroxin Pex26p recruits the Pex1p–Pex6p AAA ATPase complexes to peroxisomes

S. Tamura, Y. Fujiki, Naomi Matsumoto, 2003, Nature Cell Biology.

Mutations in the Peroxin Pex26p Responsible for Peroxisome Biogenesis Disorders of Complementation Group 8 Impair Its Stability, Peroxisomal Localization, and Interaction with the Pex1p·Pex6p Complex*

Ann Moser, H. Moser, A. Moser, 2006, Journal of Biological Chemistry.

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

Wendy K. Chung, W. Chung, Liyong Deng, 2018, Cold Spring Harbor molecular case studies.

Peroxisome biogenesis in mammalian cells

K. Okumoto, S. Tamura, Y. Fujiki, 2014, Front. Physiol..