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

od Tsukamoto, T, Shimozawa, N, Fujiki, Y
Izdano 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.

od Nakai, T, Yasuhara, T, Fujiki, Y, Ohashi, A
Izdano 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...

od Mori, T, Tsukamoto, T, Mori, H, Tashiro, Y, Fujiki, Y
Izdano 1991

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

od Miyazawa, S, Osumi, T, Hashimoto, T, Ohno, K, Miura, S, Fujiki, Y
Izdano 1989

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

od Fujiki, Y, Rachubinski, R A, Lazarow, P B
Izdano 1984

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

od Rachubinski, R A, Fujiki, Y, Lazarow, P B
Izdano 1985

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

od Shimozawa, N, Tsukamoto, T, Suzuki, Y, Orii, T, Fujiki, Y
Izdano 1992

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

od Harano, T, Nose, S, Uezu, R, Shimizu, N, Fujiki, Y
Izdano 2001

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

od Nakajima, H., Fujiki, Y., Ito, T., Kitaoka, H., Takahashi, T.
Izdano 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...

od Fukao, T, Yamaguchi, S, Kano, M, Orii, T, Fujiki, Y, Osumi, T, Hashimoto, T
Izdano 1990

Risk factors for sensitisation to methyltetrahydrophthalic anhydride.

od Yokota, K, Johyama, Y, Yamaguchi, K, Fujiki, Y, Takeshita, T, Morimoto, K
Izdano 1997

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

od Mortensen, R M, Rachubinski, R A, Fujiki, Y, Lazarow, P B
Izdano 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.

od Fujiki, Y, Rachubinski, R A, Mortensen, R M, Lazarow, P B
Izdano 1985

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

od Honsho, M, Tamura, S, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
Izdano 1998

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

od Lazarow, P B, Fujiki, Y, Small, G M, Watkins, P, Moser, H
Izdano 1986

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

od Sasaki, Y C, Yasuda, K, Suzuki, Y, Ishibashi, T, Satoh, I, Fujiki, Y, Ishiwata, S
Izdano 1997

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

od Tamura, S, Matsumoto, N, Imamura, A, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
Izdano 2001

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

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

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

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

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

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