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Synthesis and properties of 2′- O,4′- C-Ethylene-Bridged nucleic acids (ENA) as effective antisense oligonucleotides

Bioorganic & medicinal chemistry, 2003-05, Vol.11 (10), p.2211-2226

2003

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2′- O,4′- C-ethylene-bridged nucleic acids (ENA): highly nuclease-resistant and thermodynamically stable oligonucleotides for antisense drug

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (1), p.73-76

2002

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Development and Evaluation of an E-picture Book System Using Multi-directional Scrolling and Illustrations with Visual Guidance

HCI International 2017 – Posters' Extended Abstracts, p.561-568

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Biologically Stable 2-5A Analogues containing 3′-O,4′-C-bridged Adenosine as Potent RNase L Agonists

ChemMedChem, 2007-12, Vol.2 (12), p.1703-1707

2007

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Recent Development on the Studies of Nucleic Acid Antitumor Antimetabolites

Journal of Synthetic Organic Chemistry, Japan, 1991/11/01, Vol.49(11), pp.989-1001

KANEKO, Masakatsu

1991

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Interactive visual narrative "cloudy lady": gaze navigation method and a prototype application

SIGGRAPH Asia 2018 Posters, 2018, p.1-2

2018

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Synthesis and antimycobacterial activity of capuramycin analogues. Part 1: substitution of the azepan-2-one moiety of capuramycin

Bioorganic & medicinal chemistry letters, 2003-09, Vol.13 (17), p.2829-2832

2003

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Biologically Active Oligodeoxyribonucleotides. 5. 5‘-End-Substituted d(TGGGAG) Possesses Anti-Human Immunodeficiency Virus Type 1 Activity by Forming a G-Quadruplex Structure

Journal of medicinal chemistry, 1998-09, Vol.41 (19), p.3655-3663

1998

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Synthesis and antimycobacterial activity of capuramycin analogues. Part 2: acylated derivatives of capuramycin-related compounds

Bioorganic & medicinal chemistry letters, 2003-09, Vol.13 (17), p.2833-2836

2003

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Molecular Recognition of Adenophostin, a Very Potent Ca2+ Inducer, at the d-myo-Inositol 1,4,5-Trisphosphate Receptor

Biochemistry (Easton), 1999-07, Vol.38 (29), p.9234-9241

1999

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IP3 Receptor-Ligand. 1: Synthesis of Adenophostin A

Tetrahedron letters, 1995-07, Vol.36 (28), p.5037-5040

Hotoda, H

1995

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2'-0,4'-C-ethylene-bridged nucleic acids (ENA): Highly nuclease-resistant and thermodynamically stable oligonucleotides for antisense drug

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (1), p.73-76

2002

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Biologically active oligodeoxyribonucleotides--IX. Synthesis and anti-HIV-1 activity of hexadeoxyribonucleotides, TGGGAG, bearing 3'- and 5'-end-modification

Bioorganic & medicinal chemistry, 1997-12, Vol.5 (12), p.2235-2243

1997

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Stephane Mallarme a l'epoque de Divagdtions : Acheminement vers le Livre

Etudes de langue et litterature francaises, 1983, Vol.42, pp.23-44

KANEKO, Masakatsu

1983

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Studies on Griseolic Acid Derivatives. VII. Synthesis and Phosphodiesterase Inhibitory Activity of the C4'-C5' Hydrogenated Products of Griseolic Acid and Their Base-Exchanged Derivatives

Chemical and Pharmaceutical Bulletin, 1988/10/25, Vol.36(10), pp.3760-3769

1988

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Studies on Griseolic Acid Derivatives. V. Synthesis and Phosphodiesterase Inhibitory Activity of Substituted Derivatives of the Hydroxy Group at the 2'-or 7'-Position in Griseolic Acid

Chemical and Pharmaceutical Bulletin, 1987/11/25, Vol.35(11), pp.4442-4453

1987

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Studies on griseolic aicd derivatives. VI. Synthesis and phosphodiesterase-inhibitory activity of 6- and N1-substituted derivatives of griseolic acid

Chemical & pharmaceutical bulletin, 1988, Vol.36 (4), p.1309-1320

1988

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Molecular Recognition of Adenophostin, a Very Potent Ca 2+ Inducer, at the d - myo -Inositol 1,4,5-Trisphosphate Receptor

Biochemistry (Easton), 1999-07, Vol.38 (29), p.9234-9241

1999

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Biologically active oligodeoxyribonucleotides. Part 12:1 N2-Methylation of 2′-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity

Bioorganic & medicinal chemistry letters, 2000-10, Vol.10 (19), p.2213-2216

2000

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Biologically active oligodeoxyribonucleotides. Part 11: The least phosphate-modification of quadruplex-forming hexadeoxyribonucleotide TGGGAG, bearing 3′- and 5′-end-modification, with anti-HIV-1 activity

Bioorganic & medicinal chemistry, 1998-12, Vol.6 (12), p.2469-2475

1998

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Studies on Griseolic Acid Derivatives. IV. Synthesis and Phosphodiesterase Inhibitory Activity of Acylated Derivatives of Griseolic Acid

Chemical and Pharmaceutical Bulletin, 1987/03/25, Vol.35(3), pp.1036-1043

1987

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Novel Intramolecular Radical Ar-C Glycosylation-Lactonization Reaction in the Transformation of Capuramycin

Heterocycles, 2000, Vol.52 (1), p.133

2000

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Biologically active oligodeoxyribonucleotides. Part 12: 1N2-Methylation of 2′-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity

Bioorganic & medicinal chemistry letters, 2000, Vol.10 (19), p.2213-2216

2000

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Biologically active oligodeoxyribonucleotides. Part 12: N2-methylation of 2'-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity

Bioorganic & medicinal chemistry letters, 2000-10, Vol.10 (19), p.2213-2216

2000

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The Crystal and Molecular Strucure of Arabinofuranosyladenine Hydrochloride

Bulletin of the Chemical Society of Japan, 1974-11, Vol.47 (11), p.2758-2763

1974

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Synthesis and properties of 2′- O,4′- C-Ethylene-Bridged nucleic acids (ENA) as effective antisense oligonucleotides

2′- O,4′- C-ethylene-bridged nucleic acids (ENA): highly nuclease-resistant and thermodynamically stable oligonucleotides for antisense drug

Development and Evaluation of an E-picture Book System Using Multi-directional Scrolling and Illustrations with Visual Guidance

Biologically Stable 2-5A Analogues containing 3′-O,4′-C-bridged Adenosine as Potent RNase L Agonists

Recent Development on the Studies of Nucleic Acid Antitumor Antimetabolites

Interactive visual narrative "cloudy lady": gaze navigation method and a prototype application

Synthesis and antimycobacterial activity of capuramycin analogues. Part 1: substitution of the azepan-2-one moiety of capuramycin

Biologically Active Oligodeoxyribonucleotides. 5. 5‘-End-Substituted d(TGGGAG) Possesses Anti-Human Immunodeficiency Virus Type 1 Activity by Forming a G-Quadruplex Structure

Synthesis and antimycobacterial activity of capuramycin analogues. Part 2: acylated derivatives of capuramycin-related compounds

Molecular Recognition of Adenophostin, a Very Potent Ca2+ Inducer, at the d-myo-Inositol 1,4,5-Trisphosphate Receptor

IP3 Receptor-Ligand. 1: Synthesis of Adenophostin A

2'-0,4'-C-ethylene-bridged nucleic acids (ENA): Highly nuclease-resistant and thermodynamically stable oligonucleotides for antisense drug

Biologically active oligodeoxyribonucleotides--IX. Synthesis and anti-HIV-1 activity of hexadeoxyribonucleotides, TGGGAG, bearing 3'- and 5'-end-modification

Stephane Mallarme a l'epoque de Divagdtions : Acheminement vers le Livre

Studies on Griseolic Acid Derivatives. VII. Synthesis and Phosphodiesterase Inhibitory Activity of the C4'-C5' Hydrogenated Products of Griseolic Acid and Their Base-Exchanged Derivatives

Studies on Griseolic Acid Derivatives. V. Synthesis and Phosphodiesterase Inhibitory Activity of Substituted Derivatives of the Hydroxy Group at the 2'-or 7'-Position in Griseolic Acid

Studies on griseolic aicd derivatives. VI. Synthesis and phosphodiesterase-inhibitory activity of 6- and N1-substituted derivatives of griseolic acid

Molecular Recognition of Adenophostin, a Very Potent Ca 2+ Inducer, at the d - myo -Inositol 1,4,5-Trisphosphate Receptor

Biologically active oligodeoxyribonucleotides. Part 12:1 N2-Methylation of 2′-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity

Biologically active oligodeoxyribonucleotides. Part 11: The least phosphate-modification of quadruplex-forming hexadeoxyribonucleotide TGGGAG, bearing 3′- and 5′-end-modification, with anti-HIV-1 activity

Studies on Griseolic Acid Derivatives. IV. Synthesis and Phosphodiesterase Inhibitory Activity of Acylated Derivatives of Griseolic Acid

Novel Intramolecular Radical Ar-C Glycosylation-Lactonization Reaction in the Transformation of Capuramycin

Biologically active oligodeoxyribonucleotides. Part 12: 1N2-Methylation of 2′-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity

Biologically active oligodeoxyribonucleotides. Part 12: N2-methylation of 2'-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity

The Crystal and Molecular Strucure of Arabinofuranosyladenine Hydrochloride

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