S. Tamura

发表

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

T. Tsukamoto, N. Shimozawa, K. Okumoto, 1998, Molecular and Cellular Biology.

Molecular Basis for Peroxisome Biogenesis Disorders

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

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.

K. Okumoto, S. Tamura, Y. Fujiki, 2012, Biochimica et biophysica acta.

Peroxisome biogenesis and molecular defects in peroxisome assembly disorders

K. Okumoto, S. Tamura, Y. Fujiki, 2007, Cell Biochemistry and Biophysics.

Peroxisome Deficiency Impairs BDNF Signaling and Memory

T. Yamashita, S. Tamura, Y. Fujiki, 2020, Frontiers in Cell and Developmental Biology.

Peroxisome Biogenesis Disorders.

K. Okumoto, S. Tamura, Y. Fujiki, 2020, Advances in experimental medicine and biology.

Peroxisome: Metabolic Functions and Biogenesis.

K. Okumoto, S. Tamura, Y. Fujiki, 2020, Advances in experimental medicine and biology.

Mitotic phosphorylation of Pex14p regulates peroxisomal import machinery

H. Kosako, S. Tamura, Y. Fujiki, 2020, The Journal of cell biology.

Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis.

S. Tamura, Y. Fujiki, Non Miyata, 2008, Biochemical Society transactions.

Monomer-dimer transition of the conserved N-terminal domain of the mammalian peroxisomal matrix protein import receptor, Pex14p.

Jianrui Su, K. Miki, S. Tamura, 2010, Biochemical and biophysical research communications.

Dynamic and Functional Assembly of the AAA Peroxins, Pex1p and Pex6p, and Their Membrane Receptor Pex26p*

S. Tamura, Y. Fujiki, N. Matsumoto, 2006, Journal of Biological Chemistry.

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

S. Tamura, Y. Fujiki, N. Matsumoto, 2014, The Journal of Biological Chemistry.

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p.

T. Tsukamoto, Y. Suzuki, N. Shimozawa, 1998, Biochemical and biophysical research communications.

Blue Native PAGE: Applications to Study Peroxisome Biogenesis.

K. Okumoto, S. Tamura, Y. Fujiki, 2017, Methods in molecular biology.

Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.

R. Wanders, Y. Suzuki, N. Shimozawa, 1999, Human molecular genetics.

The Peroxin Pex14p

K. Ghaedi, K. Okumoto, S. Tamura, 1999, The Journal of Biological Chemistry.

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

R. Wanders, R. Wanders, K. Ghaedi, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Y. Suzuki, N. Shimozawa, S. Tamura, 1998, American journal of human genetics.

The peroxin pex3p initiates membrane assembly in peroxisome biogenesis.

K. Ghaedi, K. Okumoto, S. Tamura, 2000, Molecular biology of the cell.

Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.

H. Moser, A. Moser, N. Shimozawa, 2003, American journal of human genetics.

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 1999, Experimental cell research.

Recruiting Mechanism of the AAA Peroxins, Pex1p and Pex6p, to Pex26p on the Peroxisomal Membrane

S. Tamura, Y. Fujiki, T. Matsuzaki, 2011, Traffic.

Peroxisome Biogenesis Disorders.

K. Okumoto, S. Tamura, Y. Fujiki, 2006, Advances in experimental medicine and 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.

Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 1999, Experimental cell research.

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.

T. Tsukamoto, A. Imamura, Y. Suzuki, 1998, Human molecular genetics.

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.

Y. Suzuki, N. Shimozawa, K. Okumoto, 1998, Human molecular genetics.

Clofibrate‐inducible, 28‐kDa peroxisomal integral membrane protein is encoded by PEX11

K. Okumoto, S. Tamura, Y. Fujiki, 1998, FEBS letters.

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

T. Tsukamoto, Y. Suzuki, N. Shimozawa, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Peroxisome biogenesis in mammalian cells

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

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

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

A Mouse Model System to Study Peroxisomal Roles in Neurodegeneration of Peroxisome Biogenesis Disorders.

S. Tamura, Y. Fujiki, M. Honsho, 2020, Advances in experimental medicine and biology.

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6

H. Moser, A. Moser, N. Braverman, 2001, Journal of Human Genetics.

Recent insights into peroxisome biogenesis and associated diseases

W. Chung, T. Kuroiwa, T. Yamashita, 2020, Journal of Cell Science.

Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.

Y Fujiki, A. Imamura, Y. Suzuki, 2001, The Biochemical journal.

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.

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

Jianrui Su, K. Miki, S. Tamura, 2008, Proceedings of the National Academy of Sciences.