Y. Okada

发表

Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain

A. Yasui, H. Okayama, Kiyoji Tanaka, 1990, Nature.

High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene

T. Ishikawa, Y. Nakatsu, H. Nakane, 1995, Nature.

Characterization of a splicing mutation in group A xeroderma pigmentosum.

K. Tanaka, N. Miura, I. Satokata, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Molecular basis of group A xeroderma pigmentosum: A missense mutation and two deletions located in a zinc finger consensus sequence of the XPAC gene

Kiyoji Tanaka, I. Satokata, Y. Okada, 1992, Human Genetics.

Allelic heterogeneity in Group A xeroderma pigmentosum

K. Tanaka, N. Tachi, Y. Okada, 1992, Acta neurologica Scandinavica.

Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum.

T. Uchida, I. Satokata, Y. Okada, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Restoration of ultraviolet-induced unscheduled DNA synthesis of xeroderma pigmentosum cells by the concomitant treatment with bacteriophage T4 endonuclease V and HVJ (Sendai virus).

K. Tanaka, Y. Okada, M. Sekiguchi, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Unscheduled DNA synthesis induced by 4-nitroquinoline-1-oxide in xeroderma pigmentosum cells and their complementing heterodikaryons

H. Takebe, Kiyoji Tanaka, Y. Okada, 1980, Somatic cell genetics.

Genetic complementation groups in Cockayne syndrome

M. Ikenaga, Kiyoji Tanaka, Y. Okada, 1981, Somatic cell genetics.

The XPA protein is a zinc metalloprotein with an ability to recognize various kinds of DNA damage.

K. Tanaka, E. Ohtsuka, I. Kuraoka, 1994, Mutation research.

Identification and characterization of xpac protein, the gene product of the human XPAC (xeroderma pigmentosum group A complementing) gene.

K. Tanaka, N. Miura, I. Satokata, 1991, The Journal of biological chemistry.

Amino acids and peptides. X. Synthesis of two dotriacontapeptides corresponding to C-terminal sequence 30–61 (fragment α) of human liver metallothionein II and their heavy metal binding properties

Keiichi Tanaka, Y. Okada, K. Min, 1984 .

Fate of cadmium bound to phytochelatin in rats.

Y. Okada, K. Min, S. Onosaka, 1993, Research communications in chemical pathology and pharmacology.

High concentration of pancreatic metallothionein in normal mice.

Y. Okada, K. Min, S. Iguchi, 1988, Toxicology.

Roles of nuclear and cytoplasmic environments in the retarded DNA synthesis in Werner syndrome cells.

Y. Okada, Y. Kumahara, T. Nakazawa, 1980, Experimental cell research.

Specific action of T4 endonuclease V on damaged DNA in xeroderma pigmentosum cells in vivo.

K. Tanaka, H. Hayakawa, Y. Okada, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Establishment of Cockayne syndrome fibroblast cell line belonging to complementation group B by SV40 transformation

T. Uchida, Kiyoji Tanaka, Y. Okada, 1985, Japanese Journal of Human Genetics.

Increase in DNA synthesis in Werner's syndrome cells by hybridization with normal human diploid and HeLa cells.

Y. Okada, Y. Kumahara, T. Nakazawa, 1979, Experimental cell research.

Elevated spontaneous mutation rate in SV40-transformed werner syndrome fibroblast cell lines

J. Nakura, T. Uchida, Kiyoji Tanaka, 1985, Somatic cell and molecular genetics.

Tissue distribution of cadmium and nephropathy after administration of cadmium in several chemical forms.

Y. Okada, K. Min, S. Onosaka, 1986, Toxicology and applied pharmacology.

Portion-selective uptake of 109Cd-labelled alpha-fragment and hexapeptide of metallothionein in renal proximal tubules.

Y. Okada, K. Tanaka, K. Suzuki, 1986, Nihon eiseigaku zasshi. Japanese journal of hygiene.

A human enzyme that liberates uracil from DNA.

H. Hayakawa, Y. Okada, K. Tanaka, 1976, Biochemical and biophysical research communications.

Expression and Functional Analyses of the Dxpa Gene, the Drosophila Homolog of the Human Excision Repair Gene XPA(*)

T. Tanimura, K. Sugasawa, F. Hanaoka, 1995, The Journal of Biological Chemistry.

Three nonsense mutations responsible for group A xeroderma pigmentosum.

K. Tanaka, N. Miura, I. Satokata, 1992, Mutation research.

Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosum.

K. Tanaka, I. Satokata, Y. Okada, 1992, Mutation research.

Genomic characterization of the human DNA excision repair-controlling gene XPAC.

K. Tanaka, I. Satokata, Y. Okada, 1993, Gene.

Molecular cloning of human XPAC gene homologs from chicken, Xenopus laevis and Drosophila melanogaster.

K Tanaka, K. Tanaka, K. Kohno, 1991, Biochemical and biophysical research communications.

Protective role of renal metallothionein against Cd nephropathy in rats.

Y. Okada, K. Min, S. Onosaka, 1987, Toxicology and applied pharmacology.