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Epidemiology of herpes zoster and its relationship to varicella in Japan: A 10-year survey of 48,388 herpes zoster cases in Miyazaki prefecture

Journal of medical virology, 2009-12, Vol.81 (12), p.2053-2058

2009

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Reactions in liquid ammonia. 3. Complete aminoethylation of thiol groups in peptides and proteins by ethylenimmine in liquid ammonia

The Journal of biological chemistry, 1972-09, Vol.247 (17), p.5646-5647

1972

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Stoichiometry of the interaction of human plasma alpha 1-proteinase inhibitor with subtilisin BPN

Journal of biochemistry (Tokyo), 1989-01, Vol.105 (1), p.66-71

1989

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Studies of Peptide Antibiotics. XX. Synthesis of Tyrocidine B

Bulletin of the Chemical Society of Japan, 1970, Vol.43 (7), p.2199-2204

1970

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Trypsin reactive site of the Vicia angustifolia proteinase inhibitor [broad beans]

Journal of biochemistry (Tokyo), 1978-06, Vol.83 (6), p.1749-1756

1978

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Stoichiometry of the interaction of human plasma alpha sub(1)-proteinase inhibitor with subtilisin BPN

Journal of biochemistry (Tokyo), 1989-01, Vol.105 (1), p.66-71

1989

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Synthesis of tyrocidine B

Experientia, 1970-06, Vol.26 (6), p.587-588

1970

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Studies of Peptide Antibiotics. XV. The Synthesis of cyclo-(L-Valyl-L-ornithyl-L-leueyl-D-phenylalanyl-L-prolyl-glycyl-glycyl)

Bulletin of the Chemical Society of Japan, 1970, Vol.43 (3), p.914-917

1970

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Stoichiometry of the Interaction of Human Plasma α1 -Proteinase Inhibitor with Subtilisin BPN

Journal of biochemistry (Tokyo), 1989-01, Vol.105 (1), p.66-71

1989

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ChemInform Abstract: CATALYTIC HYDROGENOLYSIS IN LIQUID AMMONIA, STABILITY AND CLEAVAGE OF SOME PROTECTING GROUPS USED IN PEPTIDE SYNTHESIS

Chemischer Informationsdienst, 1974-12, Vol.5 (52)

1974

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Fluorescence labeling of a single sulfhydryl group in human plasma alpha 1-proteinase inhibitor and characterization of the labeled inhibitor

Journal of biochemistry (Tokyo), 1986-09, Vol.100 (3), p.563-570

1986

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Fluorescence labeling of a single sulfhydryl group in human plasma alpha sub(1)-proteinase inhibitor and characterization of the labeled inhibitor

Journal of biochemistry (Tokyo), 1986-01, Vol.100 (3), p.563-570

1986

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Removal of the N alpha-benzyloxycarbonyl group from cysteine-containing peptides by catalytic hydrogenolysis in liquid ammonia, exemplified by a synthesis of oxytocin

Journal of the American Chemical Society, 1974-07, Vol.96 (15), p.4978-4981

1974

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Fluorescence Labeling of a Single Sulfhydryl Group in Human Plasma α1-Proteinase Inhibitor and Characterization of the Labeled Inhibitor

Journal of biochemistry (Tokyo), 1986, Vol.100 (3), p.563-570

1986

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Spontaneous deamidation of a protein antibiotic, neocarzinostatin, at weakly acidic pH. Conversion to a homologous inactive preneocarzinostatin due to change of asparagine 83 to aspartic acid 83 accompanied by conformational and biological alterations

Journal of biochemistry (Tokyo), 1977-01, Vol.81 (1), p.25

1977

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Primary Structure of Neocarzinostatin, an Antitumor Protein

Science (American Association for the Advancement of Science), 1972-11, Vol.178 (4063), p.875-876

1972

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High sensitive method for determination of esterase activity of alpha -chymotrypsin and alpha -chymotrypsin-like enzymes using micro high-performance liquid chromatography

Journal of Chromatography A, 1983-01, Vol.267 (1), p.199-208

1983

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Proteinase inhibitor from Vicia angustifolia L. var. segetalis Koch. Isolation, characterization, and chemical modification

Journal of biochemistry (Tokyo), 1978-06, Vol.83 (6), p.1737-1748

1978

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ChemInform Abstract: SYNTH. DES TYROCIDINS B

Chemischer informationsdienst. Organische Chemie, 1970-09, Vol.1 (38)

1970

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ChemInform Abstract: SYNTH. VON TYROCIDIN C

Chemischer informationsdienst. Organische Chemie, 1970-07, Vol.1 (29)

1970

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Synthesis of tyrocidine B1

Experientia, 1970-06, Vol.26 (6), p.587-588

1970

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Trypsin reactivity site of the Vicia angustifolia proteinase inhibitor

Journal of biochemistry (Tokyo), 1978-06, Vol.83 (6), p.1749-1756

1978

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Synthesis of analogs of K-582A, an antibiotic heptapeptide

International Journal of Peptide and Protein Research, 1985-06, Vol.25 (6), p.640-647

1985

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Spontaneous deamidation of a protein antibiotic, neocarzinostatin, at weakly acidic pH: Conversion to a homologous inactive preneocarzinostatin due to change of asparagine 83 to aspartic acid 83 accompanied by conformational and biologic alterations

Journal of biochemistry (Tokyo), 1977-01, Vol.81 (1)

1977

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An improved synthesis of gramicidin S via solid-phase. Synthesis and cyclization by the azide method

Journal of the American Chemical Society, 1971-10, Vol.93 (20), p.5251-5254

1971

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Epidemiology of herpes zoster and its relationship to varicella in Japan: A 10-year survey of 48,388 herpes zoster cases in Miyazaki prefecture

Reactions in liquid ammonia. 3. Complete aminoethylation of thiol groups in peptides and proteins by ethylenimmine in liquid ammonia

Stoichiometry of the interaction of human plasma alpha 1-proteinase inhibitor with subtilisin BPN

Studies of Peptide Antibiotics. XX. Synthesis of Tyrocidine B

Trypsin reactive site of the Vicia angustifolia proteinase inhibitor [broad beans]

Stoichiometry of the interaction of human plasma alpha sub(1)-proteinase inhibitor with subtilisin BPN

Synthesis of tyrocidine B

Studies of Peptide Antibiotics. XV. The Synthesis of cyclo-(L-Valyl-L-ornithyl-L-leueyl-D-phenylalanyl-L-prolyl-glycyl-glycyl)

Stoichiometry of the Interaction of Human Plasma α1 -Proteinase Inhibitor with Subtilisin BPN

ChemInform Abstract: CATALYTIC HYDROGENOLYSIS IN LIQUID AMMONIA, STABILITY AND CLEAVAGE OF SOME PROTECTING GROUPS USED IN PEPTIDE SYNTHESIS

Fluorescence labeling of a single sulfhydryl group in human plasma alpha 1-proteinase inhibitor and characterization of the labeled inhibitor

Fluorescence labeling of a single sulfhydryl group in human plasma alpha sub(1)-proteinase inhibitor and characterization of the labeled inhibitor

Removal of the N alpha-benzyloxycarbonyl group from cysteine-containing peptides by catalytic hydrogenolysis in liquid ammonia, exemplified by a synthesis of oxytocin

Fluorescence Labeling of a Single Sulfhydryl Group in Human Plasma α1-Proteinase Inhibitor and Characterization of the Labeled Inhibitor

Spontaneous deamidation of a protein antibiotic, neocarzinostatin, at weakly acidic pH. Conversion to a homologous inactive preneocarzinostatin due to change of asparagine 83 to aspartic acid 83 accompanied by conformational and biological alterations

Primary Structure of Neocarzinostatin, an Antitumor Protein

High sensitive method for determination of esterase activity of alpha -chymotrypsin and alpha -chymotrypsin-like enzymes using micro high-performance liquid chromatography

Proteinase inhibitor from Vicia angustifolia L. var. segetalis Koch. Isolation, characterization, and chemical modification

ChemInform Abstract: SYNTH. DES TYROCIDINS B

ChemInform Abstract: SYNTH. VON TYROCIDIN C

Synthesis of tyrocidine B1

Trypsin reactivity site of the Vicia angustifolia proteinase inhibitor

Synthesis of analogs of K-582A, an antibiotic heptapeptide

Spontaneous deamidation of a protein antibiotic, neocarzinostatin, at weakly acidic pH: Conversion to a homologous inactive preneocarzinostatin due to change of asparagine 83 to aspartic acid 83 accompanied by conformational and biologic alterations

An improved synthesis of gramicidin S via solid-phase. Synthesis and cyclization by the azide method

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