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

著者: Tsukamoto, T, Shimozawa, N, Fujiki, Y
出版事項 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.

著者: Nakai, T, Yasuhara, T, Fujiki, Y, Ohashi, A
出版事項 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...

著者: Mori, T, Tsukamoto, T, Mori, H, Tashiro, Y, Fujiki, Y
出版事項 1991

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

著者: Miyazawa, S, Osumi, T, Hashimoto, T, Ohno, K, Miura, S, Fujiki, Y
出版事項 1989

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

著者: Fujiki, Y, Rachubinski, R A, Lazarow, P B
出版事項 1984

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

著者: Rachubinski, R A, Fujiki, Y, Lazarow, P B
出版事項 1985

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

著者: Shimozawa, N, Tsukamoto, T, Suzuki, Y, Orii, T, Fujiki, Y
出版事項 1992

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

著者: Harano, T, Nose, S, Uezu, R, Shimizu, N, Fujiki, Y
出版事項 2001

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

著者: Nakajima, H., Fujiki, Y., Ito, T., Kitaoka, H., Takahashi, T.
出版事項 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...

著者: Fukao, T, Yamaguchi, S, Kano, M, Orii, T, Fujiki, Y, Osumi, T, Hashimoto, T
出版事項 1990

Risk factors for sensitisation to methyltetrahydrophthalic anhydride.

著者: Yokota, K, Johyama, Y, Yamaguchi, K, Fujiki, Y, Takeshita, T, Morimoto, K
出版事項 1997

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

著者: Mortensen, R M, Rachubinski, R A, Fujiki, Y, Lazarow, P B
出版事項 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.

著者: Fujiki, Y, Rachubinski, R A, Mortensen, R M, Lazarow, P B
出版事項 1985

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

著者: Honsho, M, Tamura, S, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
出版事項 1998

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

著者: Lazarow, P B, Fujiki, Y, Small, G M, Watkins, P, Moser, H
出版事項 1986

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

著者: Sasaki, Y C, Yasuda, K, Suzuki, Y, Ishibashi, T, Satoh, I, Fujiki, Y, Ishiwata, S
出版事項 1997

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

著者: Tamura, S, Matsumoto, N, Imamura, A, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
出版事項 2001

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

著者: Manohar, C U, McCrady, S K, Fujiki, Y, Pavlidis, I T, Levine, J A
出版事項 2011

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

著者: Imamura, A, Tsukamoto, T, Shimozawa, N, Suzuki, Y, Zhang, Z, Imanaka, T, Fujiki, Y, Orii, T, Kondo, N, Osumi, T
出版事項 1998

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

著者: Shimozawa, N., Imamura, A., Zhang, Z., Suzuki, Y., Orii, T., Tsukamoto, T., Osumi, T., Fujiki, Y., Wanders, R., Besley, G., Kondo, N.
出版事項 1999