Yukio Fujiki

发表

Prenatal diagnosis of Zellweger syndrome using DNA analysis

T. Tsukamoto, N. Shimozawa, Yasuyuki Suzuki, 1993, Prenatal diagnosis.

A human gene responsible for Zellweger syndrome that affects peroxisome assembly.

T. Tsukamoto, Y. Suzuki, N. Shimozawa, 1992, Science.

A unified nomenclature for peroxisome biogenesis factors

H. Moser, D. Valle, H. Tabak, 1996, The Journal of cell biology.

Molecular defects in genetic diseases of peroxisomes.

Y. Fujiki, Yukio Fujiki, 1997, Biochimica et biophysica acta.

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

Y Fujiki, A. Imamura, Y. Suzuki, 2001, The Biochemical journal.

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

Y. Fujiki, T. Harano, S. Nose, 2001, The Biochemical journal.

The peroxin pex3p initiates membrane assembly in peroxisome biogenesis.

K. Ghaedi, K. Okumoto, S. Tamura, 2000, Molecular biology of the cell.

A unified nomenclature for peroxisome biogenesis factors

H. Tabak, J. Cregg, T. Tsukamoto, 1996, The Journal of cell biology.

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

R. Wanders, R. Wanders, K. Ghaedi, 1999, Proceedings of the National Academy of Sciences of the United States of America.

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

Y. Suzuki, N. Shimozawa, S. Tamura, 1998, American journal of human genetics.

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.

Y. Suzuki, N. Shimozawa, K. Okumoto, 1998, Human molecular genetics.

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

K. Ghaedi, Y. Suzuki, N. Shimozawa, 2000, American journal of human genetics.

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

T. Tsukamoto, N. Shimozawa, Y. Fujiki, 1994, Molecular and cellular biology.

Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.

K. Ghaedi, A. Imamura, Y. Suzuki, 2000, Human molecular genetics.

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p.

T. Tsukamoto, Y. Suzuki, N. Shimozawa, 1998, Biochemical and biophysical research communications.