R. Kondo

Publication List Details

Period

1993 - 2006

Number

17

Co-Authors

Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs.

Horai, S, Hayasaka, K, Kondo, R, Tsugane, K, Takahata, N

We analyzed the complete mitochondrial DNA (mtDNA) sequences of three humans (African, European, and Japanese), three African apes (common and pygmy chimpanzees, and gorilla), and one orangutan in an...

Degradation of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans by the white rot fungus Phanerochaete sordida YK-624.

Takada, S, Nakamura, M, Matsueda, T, Kondo, R, Sakai, K

A method for the degradation of dioxins by white rot fungi was developed. Degradation of a mixture of 10 kinds of tetra- to octachlorodibenzo-p-dioxins (polychlorinated dibenzo-p-dioxins [PCDDs]) and...

Bleaching of Hardwood Kraft Pulp with Manganese Peroxidase from Phanerochaete sordida YK-624 without Addition of MnSO(inf4)

Harazono, K., Kondo, R., Sakai, K.

In vitro bleaching of an unbleached hardwood kraft pulp was performed with partially purified manganese peroxidase (MnP) from the fungus Phanerochaete sordida YK-624 without the addition of...

Incomplete Maternal Transmission of Mitochondrial DNA in Drosophila

Kondo, R., Satta, Y., Matsuura, E. T., Ishiwa, H., Takahata, N., Chigusa, S. I.

The possibility of incomplete maternal transmission of mitochondrial DNA (mtDNA) in Drosophila, previously suggested by the presence of heteroplasmy, was examined by intra- and interspecific...

Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy.

Kondo, R, Wakamatsu, N, Yoshino, H, Fukuhara, N, Miyatake, T, Tsuji, S

To analyze the genetic abnormality in a Japanese patient with adult-type metachromatic leukodystrophy (MLD), we first elucidated the genomic organization of the human arylsulfatase A (ASA) gene and...

Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs.

Horai, S, Hayasaka, K, Kondo, R, Tsugane, K, Takahata, N

We analyzed the complete mitochondrial DNA (mtDNA) sequences of three humans (African, European, and Japanese), three African apes (common and pygmy chimpanzees, and gorilla), and one orangutan in an...

Degradation of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans by the white rot fungus Phanerochaete sordida YK-624.

Takada, S, Nakamura, M, Matsueda, T, Kondo, R, Sakai, K

A method for the degradation of dioxins by white rot fungi was developed. Degradation of a mixture of 10 kinds of tetra- to octachlorodibenzo-p-dioxins (polychlorinated dibenzo-p-dioxins [PCDDs]) and...

Incomplete Maternal Transmission of Mitochondrial DNA in Drosophila

Kondo, R., Satta, Y., Matsuura, E. T., Ishiwa, H., Takahata, N., Chigusa, S. I.

The possibility of incomplete maternal transmission of mitochondrial DNA (mtDNA) in Drosophila, previously suggested by the presence of heteroplasmy, was examined by intra- and interspecific...

Bleaching of Hardwood Kraft Pulp with Manganese Peroxidase from Phanerochaete sordida YK-624 without Addition of MnSO(inf4)

Harazono, K., Kondo, R., Sakai, K.

In vitro bleaching of an unbleached hardwood kraft pulp was performed with partially purified manganese peroxidase (MnP) from the fungus Phanerochaete sordida YK-624 without the addition of...

Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy.

Kondo, R, Wakamatsu, N, Yoshino, H, Fukuhara, N, Miyatake, T, Tsuji, S

To analyze the genetic abnormality in a Japanese patient with adult-type metachromatic leukodystrophy (MLD), we first elucidated the genomic organization of the human arylsulfatase A (ASA) gene and...

Mutations producing premature termination of translation and an amino acid substitution in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis associated with parkinsonism

Wakamatsu, N., Hayashi, M., Kawai, H., Kondo, H., Gotoda, Y., Nishida, Y., ...

OBJECTIVES—Mutational analysis of the sterol 27-hydroxylase (CYP27) gene was performed on three patients from two Japanese families who had cerebrotendinous xanthomatosis (CTX) associated with...