Y Fujiki|K Okumoto - JoVE Visualize

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The Journal of Biological Chemistry|June 6, 2000

Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10pK Okumoto, I Abe, Y Fujiki

Cell Biochemistry and Biophysics|May 2, 2001

Peroxisome biogenesis and molecular defects in peroxisome assembly disordersY Fujiki, K Okumoto, H Otera, et al.

FEBS Letters|August 26, 1998

Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11I Abe, K Okumoto, S Tamura, et al.

Molecular Biology of the Cell|June 10, 2000

The peroxin pex3p initiates membrane assembly in peroxisome biogenesisK Ghaedi, S Tamura, K Okumoto, et al.

Human Molecular Genetics|August 13, 1998

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group BK Okumoto, R Itoh, N Shimozawa, et al.

Experimental Cell Research|May 1, 1999

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent proteinK Ghaedi, A Kawai, K Okumoto, et al.

Biochemical and Biophysical Research Communications|January 13, 1997

Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptorT Tsukamoto, A Bogaki, K Okumoto, et al.

European Journal of Cell Biology|August 1, 1997

Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammalsK Tateishi, K Okumoto, N Shimozawa, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group IS Tamura, K Okumoto, R Toyama, et al.

Experimental Cell Research|May 25, 1997

Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group IIIK Okumoto, A Bogaki, K Tateishi, et al.

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The Journal of Biological Chemistry|June 6, 2000

Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10pK Okumoto, I Abe, Y Fujiki

Cell Biochemistry and Biophysics|May 2, 2001

Peroxisome biogenesis and molecular defects in peroxisome assembly disordersY Fujiki, K Okumoto, H Otera, et al.

FEBS Letters|August 26, 1998

Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11I Abe, K Okumoto, S Tamura, et al.

Molecular Biology of the Cell|June 10, 2000

The peroxin pex3p initiates membrane assembly in peroxisome biogenesisK Ghaedi, S Tamura, K Okumoto, et al.

Human Molecular Genetics|August 13, 1998

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group BK Okumoto, R Itoh, N Shimozawa, et al.

Experimental Cell Research|May 1, 1999

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent proteinK Ghaedi, A Kawai, K Okumoto, et al.

Biochemical and Biophysical Research Communications|January 13, 1997

Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptorT Tsukamoto, A Bogaki, K Okumoto, et al.

European Journal of Cell Biology|August 1, 1997

Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammalsK Tateishi, K Okumoto, N Shimozawa, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group IS Tamura, K Okumoto, R Toyama, et al.

Experimental Cell Research|May 25, 1997

Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group IIIK Okumoto, A Bogaki, K Tateishi, et al.

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