Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis.

le Tsukamoto, T, Shimozawa, N, Fujiki, Y
Foilsithe 1994

Multiple genes, including a member of the AAA family, are essential for degradation of unassembled subunit 2 of cytochrome c oxidase in yeast mitochondria.

le Nakai, T, Yasuhara, T, Fujiki, Y, Ohashi, A
Foilsithe 1995

Molecular cloning and deduced amino acid sequence of nonspecific lipid transfer protein (sterol carrier protein 2) of rat liver: a higher molecular mass (60 kDa) protein contains t...

le Mori, T, Tsukamoto, T, Mori, H, Tashiro, Y, Fujiki, Y
Foilsithe 1991

Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus.

le Miyazawa, S, Osumi, T, Hashimoto, T, Ohno, K, Miura, S, Fujiki, Y
Foilsithe 1989

Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes.

le Fujiki, Y, Rachubinski, R A, Lazarow, P B
Foilsithe 1984

Cloning of cDNA coding for peroxisomal acyl-CoA oxidase from the yeast Candida tropicalis pK233.

le Rachubinski, R A, Fujiki, Y, Lazarow, P B
Foilsithe 1985

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

le Shimozawa, N, Tsukamoto, T, Suzuki, Y, Orii, T, Fujiki, Y
Foilsithe 1992

Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1.

le Harano, T, Nose, S, Uezu, R, Shimizu, N, Fujiki, Y
Foilsithe 2001

Anti-Aquaporin-4 Antibody-Positive Neuromyelitis Optica Presenting with Syndrome of Inappropriate Antidiuretic Hormone Secretion as an Initial Manifestation

le Nakajima, H., Fujiki, Y., Ito, T., Kitaoka, H., Takahashi, T.
Foilsithe 2011

Molecular cloning and sequence of the complementary DNA encoding human mitochondrial acetoacetyl-coenzyme A thiolase and study of the variant enzymes in cultured fibroblasts from p...

le Fukao, T, Yamaguchi, S, Kano, M, Orii, T, Fujiki, Y, Osumi, T, Hashimoto, T
Foilsithe 1990

Risk factors for sensitisation to methyltetrahydrophthalic anhydride.

le Yokota, K, Johyama, Y, Yamaguchi, K, Fujiki, Y, Takeshita, T, Morimoto, K
Foilsithe 1997

Heating RNA before cell-free translation is essential for the efficient and reproducible synthesis of several peroxisomal proteins.

le Mortensen, R M, Rachubinski, R A, Fujiki, Y, Lazarow, P B
Foilsithe 1984

Synthesis of 3-ketoacyl-CoA thiolase of rat liver peroxisomes on free polyribosomes as a larger precursor. Induction of thiolase mRNA activity by clofibrate.

le Fujiki, Y, Rachubinski, R A, Mortensen, R M, Lazarow, P B
Foilsithe 1985

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

le Honsho, M, Tamura, S, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
Foilsithe 1998

Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).

le Lazarow, P B, Fujiki, Y, Small, G M, Watkins, P, Moser, H
Foilsithe 1986

Two-dimensional arrangement of a functional protein by cysteine-gold interaction: enzyme activity and characterization of a protein monolayer on a gold substrate.

le Sasaki, Y C, Yasuda, K, Suzuki, Y, Ishibashi, T, Satoh, I, Fujiki, Y, Ishiwata, S
Foilsithe 1997

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

le Tamura, S, Matsumoto, N, Imamura, A, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
Foilsithe 2001

Evaluation of the Accuracy of a Triaxial Accelerometer Embedded into a Cell Phone Platform for Measuring Physical Activity

le Manohar, C U, McCrady, S K, Fujiki, Y, Pavlidis, I T, Levine, J A
Foilsithe 2011

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.

le Imamura, A, Tsukamoto, T, Shimozawa, N, Suzuki, Y, Zhang, Z, Imanaka, T, Fujiki, Y, Orii, T, Kondo, N, Osumi, T
Foilsithe 1998

Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders

le Shimozawa, N., Imamura, A., Zhang, Z., Suzuki, Y., Orii, T., Tsukamoto, T., Osumi, T., Fujiki, Y., Wanders, R., Besley, G., Kondo, N.
Foilsithe 1999