M. Higuchi

Publication List Details

Period

1988 - 2008

Number

73

Co-Authors

Arbitrary Choice of Basic Variables in Density Functional Theory. II. Illustrative Applications (2003)

Higuchi, K., Higuchi, M.

Our recent theory (Ref. 1) enables us to choose arbitrary quantities as the basic variables of the density functional theory. In this paper we apply it to several cases. In the case where the...

Arbitrary Choice of Basic Variables in Density Functional Theory. I. Formalism (2003)

Higuchi, M., Higuchi, K.

The Hohenberg-Kohn theorem of the density functional theory is extended by modifying the Levy constrained-search formulation. The new theorem allows us to choose arbitrary physical quantities as the...

Electronic structure and the Fermi surface of UTGa_{5} (T=Fe, Co, Rh) (2002)

Maehira, T., Higuchi, M., Hasegawa, A.

The relativistic energy-band calculations have been carried out for UFeGa_{5}, UCoGa_{5} and URhGa_{5} under the assumption that 5f-electrons are itinerant. A hybridization between the U 5f state and...

Why is the bandwidth of sodium observed to be narrower in photoemission experiments? (1999)

Yasuhara, H., Yoshinaga, S., Higuchi, M.

The experimentally predicted narrowing in the bandwidth of sodium is interpreted in terms of the non-local self-energy effect on quasi-particle energies of the electron liquid. The calculated...

Q/R site editing in kainate receptor GluR5 and GluR6 pre-mRNAs requires distant intronic sequences.

Herb, A, Higuchi, M, Sprengel, R, Seeburg, P H

RNA editing by adenosine deamination in brain-expressed pre-mRNAs for glutamate receptor (GluR) subunits alters gene-specified codons for functionally critical positions, such as the channel's Q/R...

Hemophilia A due to mutations that create new N-glycosylation sites.

Aly, A M, Higuchi, M, Kasper, C K, Kazazian, H H, Antonarakis, S E, Hoyer, L W

In studying the molecular defects responsible for cross-reacting material-positive hemophilia A, we have identified two patients in whom the nonfunctional factor VIII-like protein has abnormal,...

Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene.

Higuchi, M, Kazazian, H H, Kasch, L, Warren, T C, McGinniss, M J, Phillips, J A, ...

Hemophilia A is an X chromosome-linked disorder resulting from deficiency of factor VIII, an important protein in blood coagulation. A large number of disease-producing mutations have been reported...

Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis.

Higuchi, M, Antonarakis, S E, Kasch, L, Oldenburg, J, Economou-Petersen, E, Olek, K, ...

To date it has been difficult to characterize completely a genetic disorder, such as hemophilia A, in which the involved gene is large and unrelated affected individuals have different mutations,...

Cloning of cDNAs encoding mammalian double-stranded RNA-specific adenosine deaminase.

O'Connell, M A, Krause, S, Higuchi, M, Hsuan, J J, Totty, N F, Jenny, A, ...

Double-stranded RNA (dsRNA)-specific adenosine deaminase converts adenosine to inosine in dsRNA. The protein has been purified from calf thymus, and here we describe the cloning of cDNAs encoding...

Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine).

Arai, M, Inaba, H, Higuchi, M, Antonarakis, S E, Kazazian, H H, Fujimaki, M, ...

An immunoadsorbent method has been developed for the direct analysis of normal and variant plasma factor VIII. Using this method, the molecular defect responsible for mild hemophilia A has been...

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.

Tuddenham, E G, Schwaab, R, Seehafer, J, Millar, D S, Gitschier, J, Higuchi, M, ...

A large number of different mutations in the factor VIII (F8) gene have been identified as a cause of haemophilia A. This compilation lists known single base-pair substitutions, deletions and...

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.

Tuddenham, E G, Schwaab, R, Seehafer, J, Millar, D S, Gitschier, J, Higuchi, M, ...

A large number of different mutations in the factor VIII (F8) gene have been identified as a cause of haemophilia A. This compilation lists known single base-pair substitutions, deletions and...

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene.

Tuddenham, E G, Cooper, D N, Gitschier, J, Higuchi, M, Hoyer, L W, Yoshioka, A, ...

Mutations at the factor VIII gene locus causing Haemophilia A have now been identified in many patients from many ethnic groups. Earlier studies used biased methods which detected repetitive...

Bacteriophage deoxyribonucleic acid-induced mutation of Streptococcus mutans.

Higuchi, M, Rhee, G H, Araya, S, Higuchi, M

A cariogenic strain, Streptococcus mutans PK 1, has been demonstrated to have prophage by observation of phage particles with an electron microscope and by induction with mitomycin C. The phage...

Transfection of Streptococcus sanguis by phage deoxyribonucleic acid isolated from Streptococcus mutans.

Higuchi, M, Rhee, G H, Araya, S, Higuchi, M

Streptococcus sanguis ATCC 10556 cells were infected with free phage DNA of S, mutans strain PK 1. Two transformants were isolated which made colonies with large mucoid forms on mitis-salivarius...

Activation of CPP32-like protease in tumor necrosis factor-induced apoptosis is dependent on mitochondrial function.

Higuchi, M, Aggarwal, B B, Yeh, E T

Mitochondria have been implicated in apoptosis, however, the precise mechanisms whereby mitochondria exert their effect are not clear. To gain further insights, we generated a panel of cells from...

Q/R site editing in kainate receptor GluR5 and GluR6 pre-mRNAs requires distant intronic sequences.

Herb, A, Higuchi, M, Sprengel, R, Seeburg, P H

RNA editing by adenosine deamination in brain-expressed pre-mRNAs for glutamate receptor (GluR) subunits alters gene-specified codons for functionally critical positions, such as the channel's Q/R...

Hemophilia A due to mutations that create new N-glycosylation sites.

Aly, A M, Higuchi, M, Kasper, C K, Kazazian, H H, Antonarakis, S E, Hoyer, L W

In studying the molecular defects responsible for cross-reacting material-positive hemophilia A, we have identified two patients in whom the nonfunctional factor VIII-like protein has abnormal,...

Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene.

Higuchi, M, Kazazian, H H, Kasch, L, Warren, T C, McGinniss, M J, Phillips, J A, ...

Hemophilia A is an X chromosome-linked disorder resulting from deficiency of factor VIII, an important protein in blood coagulation. A large number of disease-producing mutations have been reported...

Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis.

Higuchi, M, Antonarakis, S E, Kasch, L, Oldenburg, J, Economou-Petersen, E, Olek, K, ...

To date it has been difficult to characterize completely a genetic disorder, such as hemophilia A, in which the involved gene is large and unrelated affected individuals have different mutations,...

Cloning of cDNAs encoding mammalian double-stranded RNA-specific adenosine deaminase.

O'Connell, M A, Krause, S, Higuchi, M, Hsuan, J J, Totty, N F, Jenny, A, ...

Double-stranded RNA (dsRNA)-specific adenosine deaminase converts adenosine to inosine in dsRNA. The protein has been purified from calf thymus, and here we describe the cloning of cDNAs encoding...

Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine).

Arai, M, Inaba, H, Higuchi, M, Antonarakis, S E, Kazazian, H H, Fujimaki, M, ...

An immunoadsorbent method has been developed for the direct analysis of normal and variant plasma factor VIII. Using this method, the molecular defect responsible for mild hemophilia A has been...

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.

Tuddenham, E G, Schwaab, R, Seehafer, J, Millar, D S, Gitschier, J, Higuchi, M, ...

A large number of different mutations in the factor VIII (F8) gene have been identified as a cause of haemophilia A. This compilation lists known single base-pair substitutions, deletions and...

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.

Tuddenham, E G, Schwaab, R, Seehafer, J, Millar, D S, Gitschier, J, Higuchi, M, ...

A large number of different mutations in the factor VIII (F8) gene have been identified as a cause of haemophilia A. This compilation lists known single base-pair substitutions, deletions and...

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene.

Tuddenham, E G, Cooper, D N, Gitschier, J, Higuchi, M, Hoyer, L W, Yoshioka, A, ...

Mutations at the factor VIII gene locus causing Haemophilia A have now been identified in many patients from many ethnic groups. Earlier studies used biased methods which detected repetitive...

Bacteriophage deoxyribonucleic acid-induced mutation of Streptococcus mutans.

Higuchi, M, Rhee, G H, Araya, S, Higuchi, M

A cariogenic strain, Streptococcus mutans PK 1, has been demonstrated to have prophage by observation of phage particles with an electron microscope and by induction with mitomycin C. The phage...

Transfection of Streptococcus sanguis by phage deoxyribonucleic acid isolated from Streptococcus mutans.

Higuchi, M, Rhee, G H, Araya, S, Higuchi, M

Streptococcus sanguis ATCC 10556 cells were infected with free phage DNA of S, mutans strain PK 1. Two transformants were isolated which made colonies with large mucoid forms on mitis-salivarius...

Activation of CPP32-like protease in tumor necrosis factor-induced apoptosis is dependent on mitochondrial function.

Higuchi, M, Aggarwal, B B, Yeh, E T

Mitochondria have been implicated in apoptosis, however, the precise mechanisms whereby mitochondria exert their effect are not clear. To gain further insights, we generated a panel of cells from...

Partial correction of a severe molecular defect in hemophilia A, because of errors during expression of the factor VIII gene.

Young, M, Inaba, H, Hoyer, L W, Higuchi, M, Kazazian, H H, Antonarakis, S E

Although the molecular defect in patients in a Japanese family with mild to moderately severe hemophilia A was a deletion of a single nucleotide T within an A8TA2 sequence of exon 14 of the factor...