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

por Tsukamoto, T, Shimozawa, N, Fujiki, Y
Publicado em 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.

por Nakai, T, Yasuhara, T, Fujiki, Y, Ohashi, A
Publicado em 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...

por Mori, T, Tsukamoto, T, Mori, H, Tashiro, Y, Fujiki, Y
Publicado em 1991

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

por Miyazawa, S, Osumi, T, Hashimoto, T, Ohno, K, Miura, S, Fujiki, Y
Publicado em 1989

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

por Fujiki, Y, Rachubinski, R A, Lazarow, P B
Publicado em 1984

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

por Rachubinski, R A, Fujiki, Y, Lazarow, P B
Publicado em 1985

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

por Shimozawa, N, Tsukamoto, T, Suzuki, Y, Orii, T, Fujiki, Y
Publicado em 1992

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

por Harano, T, Nose, S, Uezu, R, Shimizu, N, Fujiki, Y
Publicado em 2001

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

por Nakajima, H., Fujiki, Y., Ito, T., Kitaoka, H., Takahashi, T.
Publicado em 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...

por Fukao, T, Yamaguchi, S, Kano, M, Orii, T, Fujiki, Y, Osumi, T, Hashimoto, T
Publicado em 1990

Risk factors for sensitisation to methyltetrahydrophthalic anhydride.

por Yokota, K, Johyama, Y, Yamaguchi, K, Fujiki, Y, Takeshita, T, Morimoto, K
Publicado em 1997

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

por Mortensen, R M, Rachubinski, R A, Fujiki, Y, Lazarow, P B
Publicado em 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.

por Fujiki, Y, Rachubinski, R A, Mortensen, R M, Lazarow, P B
Publicado em 1985

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

por Honsho, M, Tamura, S, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
Publicado em 1998

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

por Lazarow, P B, Fujiki, Y, Small, G M, Watkins, P, Moser, H
Publicado em 1986

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

por Sasaki, Y C, Yasuda, K, Suzuki, Y, Ishibashi, T, Satoh, I, Fujiki, Y, Ishiwata, S
Publicado em 1997

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

por Tamura, S, Matsumoto, N, Imamura, A, Shimozawa, N, Suzuki, Y, Kondo, N, Fujiki, Y
Publicado em 2001

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

por Manohar, C U, McCrady, S K, Fujiki, Y, Pavlidis, I T, Levine, J A
Publicado em 2011

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

por Imamura, A, Tsukamoto, T, Shimozawa, N, Suzuki, Y, Zhang, Z, Imanaka, T, Fujiki, Y, Orii, T, Kondo, N, Osumi, T
Publicado em 1998

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

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