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Diagnosis of Potato Mop-Top Virus in Soil Using Bait Plant Bioassay and RT-PCR-microplate Hybridization

American journal of potato research, 2010-04, Vol.87 (2), p.218-225

2010

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Characterization of a SARS-CoV-2 EG.5.1 clinical isolate in vitro and in vivo

Cell reports (Cambridge), 2023-12, Vol.42 (12), p.113580-113580, Article 113580

2023

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Drinkable Preparation of Theracurmin Exhibits High Absorption Efficiency—A Single-Dose, Double-Blind, 4-Way Crossover Study

Biological and Pharmaceutical Bulletin, 2013/11/01, Vol.36(11), pp.1708-1714

2013

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Effectiveness of BA.1- and BA.4/BA. 5-Containing Bivalent COVID-19 mRNA Vaccines Against Symptomatic SARS-CoV-2 Infection During the BA.5-Dominant Period in Japan

Open forum infectious diseases, 2023-06, Vol.10 (6), p.ofad240-ofad240

2023

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C-terminal Fragment of Presenilin Is the Molecular Target of a Dipeptidic γ-Secretase-specific Inhibitor DAPT (N-[N-(3,5-Difluorophenacetyl)-L-alanyl]-S-phenylglycine t-Butyl Ester)

The Journal of biological chemistry, 2006-05, Vol.281 (21), p.14670-14676

2006

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Preparation of a polyclonal antibody that recognizes a unique galactoseβ1-4fucose disaccharide epitope

Carbohydrate research, 2015-08, Vol.412, p.50-55

2015

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Divergent Synthesis of Multifunctional Molecular Probes To Elucidate the Enzyme Specificity of Dipeptidic γ-Secretase Inhibitors

ACS chemical biology, 2007-06, Vol.2 (6), p.0-0

2007

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Synthetic studies on antascomicin A: construction of the C18–C34 fragment

Tetrahedron, 2004-06, Vol.60 (25), p.5341-5352

2004

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Highly efficient synthesis of medium-sized lactams via intramolecular Staudinger–aza-Wittig reaction of ω-azido pentafluorophenyl ester: synthesis and biological evaluation of LY411575 analogues

Tetrahedron letters, 2004-03, Vol.45 (11), p.2323-2326

2004

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Synthesis of biotinylated photoaffinity probes based on arylsulfonamide γ-secretase inhibitors

Bioorganic & medicinal chemistry letters, 2006-08, Vol.16 (16), p.4184-4189

2006

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Synthetic studies on 3-arylquinazolin-4-ones: intramolecular nucleophilic aromatic substitution reaction of 2-carboxamido-3-arylquinazolin-4-ones and its application to the synthesis of secondary aryl amines

Tetrahedron, 2005-04, Vol.61 (17), p.4297-4312

2005

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The effect of environmental temperature on distribution of unit chains of rice amylopectin

Die Stärke, 2000, Vol.52 (1), p.8-12

2000

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Novel γ-secretase inhibitors discovered by library screening of in-house synthetic natural product intermediates

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (14), p.3813-3816

2006

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Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and its Application to the Synthesis of Secondary Aryl Amines

Synlett, 2004-11, Vol.2004 (14), p.2497-2500

2004

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C-terminal Fragment of Presenilin Is the Molecular Target of a Dipeptidic Î³-Secretase-specific Inhibitor DAPT (N-[N-(3,5-Difluorophenacetyl)-L-alanyl]-S-phenylglycine t-Butyl Ester)

The Journal of biological chemistry, 2006-05, Vol.281 (21), p.14670

2006

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P4-322 Presenilin-1 is a molecular target of a dipeptidic γ-secretase inhibitor, DAPT

Neurobiology of aging, 2004-07, Vol.25, p.S566-S567

2004

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O1-02-07: Different actions of dipeptidic compounds on presenilins define the enzyme specificity of γ-secretase inhibitor

Alzheimer's & dementia, 2006-07, Vol.2 (3), p.S12-S12

2006

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Synthetic Studies on Antascomicin A: Construction of the C18-C34 Fragment (I)

ChemInform, 2004-10, Vol.35 (40), p.no-no

2004

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Synthetic Studies on 3-Arylquinazolin-4-ones: Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and Its Application to the Synthesis of Secondary Aryl Amines

ChemInform, 2005-08, Vol.36 (33), p.no-no

2005

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Synthetic Studies on 3-Arylquinazolin-4-ones: Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and Its Application to the Synthesis of Secondary Aryl Amines

ChemInform, 2005-08, Vol.36 (33), p.no-no

2005

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Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and Its Application to the Synthesis of Secondary Aryl Amines

ChemInform, 2005-04, Vol.36 (17), p.no-no

2005

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CLINICAL TRIAL OF SIMULTANEOUS INTRA-CAVITARY HYPERTHRMO-BRACHYTHERAPY FOR ESOPHAGEAL CANCER

The Journal of JASTRO, 2000/12/25, Vol.12(4), pp.371-377

2000

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Highly Efficient Synthesis of Medium-Sized Lactams via Intramolecular Staudinger-aza-Wittig Reaction of ω-Azido Pentafluorophenyl Ester: Synthesis and Biological Evaluation of LY411575 Analogues

ChemInform, 2004-06, Vol.35 (26), p.no-no

2004

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Diagnosis of Potato Mop-Top Virus in Soil Using Bait Plant Bioassay and RT-PCR-microplate Hybridization

Characterization of a SARS-CoV-2 EG.5.1 clinical isolate in vitro and in vivo

Drinkable Preparation of Theracurmin Exhibits High Absorption Efficiency—A Single-Dose, Double-Blind, 4-Way Crossover Study

Immune escape and waning immunity of COVID-19 monovalent mRNA vaccines against symptomatic infection with BA.1/BA.2 and BA.5 in Japan

Effectiveness of BA.1- and BA.4/BA. 5-Containing Bivalent COVID-19 mRNA Vaccines Against Symptomatic SARS-CoV-2 Infection During the BA.5-Dominant Period in Japan

C-terminal Fragment of Presenilin Is the Molecular Target of a Dipeptidic γ-Secretase-specific Inhibitor DAPT (N-[N-(3,5-Difluorophenacetyl)-L-alanyl]-S-phenylglycine t-Butyl Ester)

Preparation of a polyclonal antibody that recognizes a unique galactoseβ1-4fucose disaccharide epitope

Effectiveness of BA.1- and BA.4/BA.5-containing bivalent COVID-19 mRNA vaccines against symptomatic SARS-CoV-2 infection during the BA.5-dominant period in Japan

Divergent Synthesis of Multifunctional Molecular Probes To Elucidate the Enzyme Specificity of Dipeptidic γ-Secretase Inhibitors

Synthetic studies on antascomicin A: construction of the C18–C34 fragment

Highly efficient synthesis of medium-sized lactams via intramolecular Staudinger–aza-Wittig reaction of ω-azido pentafluorophenyl ester: synthesis and biological evaluation of LY411575 analogues

Synthesis of biotinylated photoaffinity probes based on arylsulfonamide γ-secretase inhibitors

Synthetic studies on 3-arylquinazolin-4-ones: intramolecular nucleophilic aromatic substitution reaction of 2-carboxamido-3-arylquinazolin-4-ones and its application to the synthesis of secondary aryl amines

The effect of environmental temperature on distribution of unit chains of rice amylopectin

Novel γ-secretase inhibitors discovered by library screening of in-house synthetic natural product intermediates

Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and its Application to the Synthesis of Secondary Aryl Amines

C-terminal Fragment of Presenilin Is the Molecular Target of a Dipeptidic Î³-Secretase-specific Inhibitor DAPT (N-[N-(3,5-Difluorophenacetyl)-L-alanyl]-S-phenylglycine t-Butyl Ester)

P4-322 Presenilin-1 is a molecular target of a dipeptidic γ-secretase inhibitor, DAPT

O1-02-07: Different actions of dipeptidic compounds on presenilins define the enzyme specificity of γ-secretase inhibitor

Synthetic Studies on Antascomicin A: Construction of the C18-C34 Fragment (I)

Synthetic Studies on 3-Arylquinazolin-4-ones: Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and Its Application to the Synthesis of Secondary Aryl Amines

Synthetic Studies on 3-Arylquinazolin-4-ones: Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and Its Application to the Synthesis of Secondary Aryl Amines

Intramolecular Nucleophilic Aromatic Substitution Reaction of 2-Carboxamido-3-arylquinazolin-4-ones and Its Application to the Synthesis of Secondary Aryl Amines

CLINICAL TRIAL OF SIMULTANEOUS INTRA-CAVITARY HYPERTHRMO-BRACHYTHERAPY FOR ESOPHAGEAL CANCER

Highly Efficient Synthesis of Medium-Sized Lactams via Intramolecular Staudinger-aza-Wittig Reaction of ω-Azido Pentafluorophenyl Ester: Synthesis and Biological Evaluation of LY411575 Analogues

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