-Ayami Matsushima Researcher Activity Profile

Research Author Detailed Information 

Ayami Matsushima Publication Rate By Year

Ayami Matsushima has published 1 paper(s) in 1967, 4 paper(s) in 1969, 1 paper(s) in 1970, 2 paper(s) in 1972, 1 paper(s) in 1973, 2 paper(s) in 1974, 1 paper(s) in 1982, 1 paper(s) in 1987, 2 paper(s) in 1997, 2 paper(s) in 2000, 1 paper(s) in 2002, 7 paper(s) in 2007, 6 paper(s) in 2008, for a total of 31 research publications in total.

Ayami A Matsushima Author Information

LAST NAME: matsushima

FIRST NAME: Ayami

INITIALS: a

AFFILIATION:

Papers

Ayami Matsushima's Publication Record

1. Double-labelled in situ hybridization reveals the lack of co-localization of mRNAs for the circadian neuropeptide PDF and FMRFamide in brains of the flies Musca domestica and Drosophila melanogaster. Year Published: 2007
Laboratory of Structure-Function Biochemistry, Department of Chemistry, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
2. Edge-to-face CH/pi interaction between ligand Phe-phenyl and receptor aromatic group in the thrombin receptor activation. Year Published: 2000
Laboratory of Structure-Function Biochemistry, Department of Chemistry, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
3. cDNA cloning and nuclear localization of the circadian neuropeptide designated as pigment-dispersing factor PDF in the cricket Gryllus bimaculatus. Year Published: 2002
Laboratory of Structure-Function Biochemistry, Department of Chemistry, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
4. States of amino acid residues in proteins. XII. Amino groups with different reactivities toward naphthoquinone sulfonic acid. Year Published: 1967
5. States of amino acid residues in proteins. XVI. Naphthoquinones with two sulfonic groups as a reagent for discrimation of amino groups in proteins. Year Published: 1969
6. Comparative studies on the states of amino acid residues in porcine and bovine trypsins. Year Published: 1969
7. States of amino acid residues in proteins. XVII. Tyrosine, histidine and tryptophan residues in bovine trypsin in the presence and absence of benzamidine. Year Published: 1969
8. Tyrosine, histidineand tryptophan residues in TPCK-modifiechymotrypsin. Year Published: 1969
9. Molecular weight and amino acid composition of equine thrombin. Year Published: 1970
10. Spectral changes of porcine trypsin induced by divalent cations. Year Published: 1972
11. Thrombin-catalyzed conversion of fibrinogen to fibrin. Year Published: 1972
12. States of imino groups in pepsin measured by the reactivity with tertiary-butylhypochlorite. Year Published: 1973
13. States on imino groups in collagen as measured with a modifying reagent, tert-butyl hypochlorite. Year Published: 1974
14. Reactivity of peptide imino groups in proteins with tert-butyl hypochlorite in relation to secondary structure. Year Published: 1974
15. Physicochemical properties and states of sulfhydryl groups of uricase from Candida utilis. Year Published: 1982
16. Region of cytochrome c interacting with yeast cytochrome b2: determination with singly modified carboxydinitrophenyl cytochromes c. Year Published: 1987
17. Double-labelled in situ hybridization reveals the lack of co-localization of mRNAs for the circadian neuropeptide PDF and FMRFamide in brains of the flies Musca domestica and Drosophila melanogaster. Year Published: 2007
Laboratory of Structure-Function Biochemistry, Department of Chemistry, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
18. Structural evidence for endocrine disruptor bisphenol a binding to human nuclear receptor ERR gamma. Year Published: 2007
Laboratory of Structure-Function Biochemistry, Department of Chemistry, Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
19. Receptor binding characteristics of the endocrine disruptor bisphenol A for the human nuclear estrogen-related receptor gamma. Chief and corroborative hydrogen bonds of the bisphenol A phenol-hydroxyl group with Arg316 and Glu275 residues. Year Published: 2007
Laboratory of Structure-Function Biochemistry, Department of Chemistry, The Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka, Japan.
20. Direct Evidence Revealing Structural Elements Essential for the High Binding Ability of Bisphenol A to Human Estrogen-Related Receptor-gamma. Year Published: 2008
Laboratory of Structure-Function Biochemistry, Department of Chemistry, The Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka, Japan.
21. Direct Evidence Revealing Structural Elements Essential for the High Binding Ability of Bisphenol A to Human Estrogen-Related Receptor-gamma. Year Published: 2008
Laboratory of Structure-Function Biochemistry, Department of Chemistry, The Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka, Japan.
22. Structural evidence for endocrine disruptor bisphenol A binding to human nuclear receptor ERR gamma. Year Published: 2007
Laboratory of Structure-Function Biochemistry, Department of Chemistry, Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
23. Receptor binding characteristics of the endocrine disruptor bisphenol A for the human nuclear estrogen-related receptor gamma. Chief and corroborative hydrogen bonds of the bisphenol A phenol-hydroxyl group with Arg316 and Glu275 residues. Year Published: 2007
Laboratory of Structure-Function Biochemistry, Department of Chemistry, The Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka, Japan.
24. An enone reductase from Nicotiana tabacum: cDNA cloning, expression in Escherichia coli, and reduction of enones with the recombinant proteins. Year Published: 2008
Natural Science Center for Basic Research and Development, Radioisotope Center, Hiroshima University, 1-4-2 Kagamiyama, Higashi-Hiroshima 739-8526, Japan.
25. Direct evidence revealing structural elements essential for the high binding ability of bisphenol A to human estrogen-related receptor-gamma. Year Published: 2008
Laboratory of Structure-Function Biochemistry, Department of Chemistry, The Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka, Japan.
26. Immune tolerance induced by polyethylene glycol-conjugate of protein antigen: clonal deletion of antigen-specific Th-cells in the thymus. Year Published: 2000
Department of Biomedical Engineering, Toin University of Yokohama, Japan.
27. Polyethylene glycol-modified pokeweed mitogen (PWM) as a potential non-immunogenic stimulator of lymphokine-activated killer cells. Year Published: 1997
Toin Human Science and Technology Center, Department of Materials Science and Technology, Toin University of Yokohama, Japan.
28. Tolerogenic capacity of poly(ethylene glycol) (PEG)--modified ovalbumins in relation to their immunoreactivity towards anti-ovalbumin antibody. Year Published: 1997
Toin Human Science and Technology Center, Department of Materials Science and Technology, Toin University of Yokohama, Japan.
29. Direct evidence revealing structural elements essential for the high binding ability of bisphenol A to human estrogen-related receptor-gamma. Year Published: 2008
Laboratory of Structure-Function Biochemistry, Department of Chemistry, The Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka, Japan.
30. Designed modification of partial agonist of ORL1 nociceptin receptor for conversion into highly potent antagonist. Year Published: 2008
Laboratory of Structure-Function Biochemistry, Department of Chemistry, Research-Education Centre of Risk Science, Faculty of Sciences, Kyushu University, Fukuoka 812-8581, Japan.
31. Receptor binding characteristics of the endocrine disruptor bisphenol A for the human nuclear estrogen-related receptor gamma. Chief and corroborative hydrogen bonds of the bisphenol A phenol-hydroxyl group with Arg316 and Glu275 residues. Year Published: 2007
Laboratory of Structure-Function Biochemistry, Department of Chemistry, The Research-Education Centre of Risk Science, Faculty and Graduate School of Sciences, Kyushu University, Fukuoka, Japan.