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Mondor's Disease: A Review of the Literature

Internal Medicine, 2018/09/15, Vol.57(18), pp.2607-2612

2018

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Emphysematous Cystitis: A Review of the Literature

Internal Medicine, 2014, Vol.53(2), pp.79-82

2014

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Third-Dose BNT162b2 Vaccination Elicits Markedly High-Level SARS-CoV-2-Neutralizing Antibodies in Vaccinees Who Responded Poorly to a Second Dose in Japan

The Journal of infectious diseases, 2022-11, Vol.226 (11), p.2038-2039

2022

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Correlates of neutralizing/SARS-CoV-2-S1-binding antibody response with adverse effects and immune kinetics in BNT162b2-vaccinated individuals

Scientific reports, 2021-11, Vol.11 (1), p.22848-10, Article 22848

2021

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A Conformational Escape Reaction of HIV-1 against an Allosteric Integrase Inhibitor

Journal of virology, 2020-09, Vol.94 (19)

2020

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Neutralization against Omicron sublineages (BA.2/BA.5/BQ.1.1/XBB/XBB.1.5) in bivalent BNT162b2-vaccinated HCWs with or without risk factors, or following BT infection with Omicron

Scientific reports, 2023-10, Vol.13 (1), p.17404-17404, Article 17404

2023

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Novel p97/VCP inhibitor induces endoplasmic reticulum stress and apoptosis in both bortezomib‐sensitive and ‐resistant multiple myeloma cells

Cancer science, 2019-10, Vol.110 (10), p.3275-3287

2019

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Neutralization activity of sera/IgG preparations from fully BNT162b2 vaccinated individuals against SARS-CoV-2 Alpha, Beta, Gamma, Delta, and Kappa variants

Scientific reports, 2022-08, Vol.12 (1), p.13524-13524, Article 13524

2022

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Human retroviral antisense mRNAs are retained in the nuclei of infected cells for viral persistence

Proceedings of the National Academy of Sciences - PNAS, 2021-04, Vol.118 (17), p.1

2021

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Structure-Based Design of Highly Potent HIV‑1 Protease Inhibitors Containing New Tricyclic Ring P2-Ligands: Design, Synthesis, Biological, and X‑ray Structural Studies

Journal of medicinal chemistry, 2020-05, Vol.63 (9), p.4867-4879

2020

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Evaluation of darunavir-derived HIV-1 protease inhibitors incorporating P2′ amide-derivatives: Synthesis, biological evaluation and structural studies

Bioorganic & medicinal chemistry letters, 2023-03, Vol.83 (C), p.129168-129168, Article 129168

2023

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Amino-acid inserts of HIV-1 capsid (CA) induce CA degradation and abrogate viral infectivity: Insights for the dynamics and mechanisms of HIV-1 CA decomposition

Scientific reports, 2019-07, Vol.9 (1), p.9806-17, Article 9806

2019

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An Autopsy Case of Streptococcus dysgalactiae subsp. equisimilis Infectious Endocarditis Accompanied by Streptococcal Toxic Shock Syndrome

Internal medicine (Tokyo, 1992), 2024-08, Vol.63 (15), p.2209-2214, Article 2526-23

2024

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Development of anti-HBV agents targeting HBV capsid proteins

RSC medicinal chemistry, 2023-10, Vol.14 (1), p.1973-198

2023

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Effectual Diagnostic Approach: A New Strategy to Achieve Diagnostic Excellence in High Diagnostic Uncertainty

International journal of general medicine, 2022-01, Vol.15, p.8327-8332

2022

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Filifactor alocis brain abscess identified by 16S ribosomal RNA gene sequencing: A case report

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2020-02, Vol.26 (2), p.305-307

2020

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Novel Central Nervous System (CNS)-Targeting Protease Inhibitors for Drug-Resistant HIV Infection and HIV-Associated CNS Complications

Antimicrobial agents and chemotherapy, 2019-07, Vol.63 (7)

2019

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4′‐modified nucleoside analogs: Potent inhibitors active against entecavir‐resistant hepatitis B virus

Hepatology (Baltimore, Md.), 2015-10, Vol.62 (4), p.1024-1036

2015

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In Vitro Selection of Highly Darunavir-Resistant and Replication-Competent HIV-1 Variants by Using a Mixture of Clinical HIV-1 Isolates Resistant to Multiple Conventional Protease Inhibitors

Journal of Virology, 2010-11, Vol.84 (22), p.11961-11969

2010

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Design, Synthesis and X‐Ray Structural Studies of Potent HIV‐1 Protease Inhibitors Containing C‐4 Substituted Tricyclic Hexahydro‐Furofuran Derivatives as P2 Ligands

ChemMedChem, 2022-05, Vol.17 (9), p.e202200058-n/a

2022

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Design and Synthesis of Potent HIV-1 Protease Inhibitors Incorporating Hexahydrofuropyranol-Derived High Affinity P2 Ligands: Structure−Activity Studies and Biological Evaluation

Journal of medicinal chemistry, 2011-01, Vol.54 (2), p.622-634

2011

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GRL-09510, a Unique P2-Crown-Tetrahydrofuranylurethane -Containing HIV-1 Protease Inhibitor, Maintains Its Favorable Antiviral Activity against Highly-Drug-Resistant HIV-1 Variants in vitro

Scientific reports, 2017-09, Vol.7 (1), p.12235-12, Article 12235

2017

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Design, synthesis, X-ray studies, and biological evaluation of novel macrocyclic HIV-1 protease inhibitors involving the P1′-P2′ ligands

Bioorganic & medicinal chemistry letters, 2017-11, Vol.27 (21), p.4925-4931

2017

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Design of novel HIV-1 protease inhibitors incorporating isophthalamide-derived P2-P3 ligands: Synthesis, biological evaluation and X-ray structural studies of inhibitor-HIV-1 protease complex

Bioorganic & medicinal chemistry, 2017-10, Vol.25 (19), p.5114-5127

2017

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Structure-based design, synthesis, X-ray studies, and biological evaluation of novel HIV-1 protease inhibitors containing isophthalamide-derived P2-ligands

Bioorganic & medicinal chemistry letters, 2015-11, Vol.25 (21), p.4903-4909

2015

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Mondor's Disease: A Review of the Literature

Emphysematous Cystitis: A Review of the Literature

Third-Dose BNT162b2 Vaccination Elicits Markedly High-Level SARS-CoV-2-Neutralizing Antibodies in Vaccinees Who Responded Poorly to a Second Dose in Japan

Correlates of neutralizing/SARS-CoV-2-S1-binding antibody response with adverse effects and immune kinetics in BNT162b2-vaccinated individuals

A Conformational Escape Reaction of HIV-1 against an Allosteric Integrase Inhibitor

Neutralization against Omicron sublineages (BA.2/BA.5/BQ.1.1/XBB/XBB.1.5) in bivalent BNT162b2-vaccinated HCWs with or without risk factors, or following BT infection with Omicron

Novel p97/VCP inhibitor induces endoplasmic reticulum stress and apoptosis in both bortezomib‐sensitive and ‐resistant multiple myeloma cells

Neutralization activity of sera/IgG preparations from fully BNT162b2 vaccinated individuals against SARS-CoV-2 Alpha, Beta, Gamma, Delta, and Kappa variants

Human retroviral antisense mRNAs are retained in the nuclei of infected cells for viral persistence

Structure-Based Design of Highly Potent HIV‑1 Protease Inhibitors Containing New Tricyclic Ring P2-Ligands: Design, Synthesis, Biological, and X‑ray Structural Studies

Evaluation of darunavir-derived HIV-1 protease inhibitors incorporating P2′ amide-derivatives: Synthesis, biological evaluation and structural studies

Amino-acid inserts of HIV-1 capsid (CA) induce CA degradation and abrogate viral infectivity: Insights for the dynamics and mechanisms of HIV-1 CA decomposition

An Autopsy Case of Streptococcus dysgalactiae subsp. equisimilis Infectious Endocarditis Accompanied by Streptococcal Toxic Shock Syndrome

Development of anti-HBV agents targeting HBV capsid proteins

Effectual Diagnostic Approach: A New Strategy to Achieve Diagnostic Excellence in High Diagnostic Uncertainty

Filifactor alocis brain abscess identified by 16S ribosomal RNA gene sequencing: A case report

Novel Central Nervous System (CNS)-Targeting Protease Inhibitors for Drug-Resistant HIV Infection and HIV-Associated CNS Complications

4′‐modified nucleoside analogs: Potent inhibitors active against entecavir‐resistant hepatitis B virus

In Vitro Selection of Highly Darunavir-Resistant and Replication-Competent HIV-1 Variants by Using a Mixture of Clinical HIV-1 Isolates Resistant to Multiple Conventional Protease Inhibitors

Design, Synthesis and X‐Ray Structural Studies of Potent HIV‐1 Protease Inhibitors Containing C‐4 Substituted Tricyclic Hexahydro‐Furofuran Derivatives as P2 Ligands

Design and Synthesis of Potent HIV-1 Protease Inhibitors Incorporating Hexahydrofuropyranol-Derived High Affinity P2 Ligands: Structure−Activity Studies and Biological Evaluation

GRL-09510, a Unique P2-Crown-Tetrahydrofuranylurethane -Containing HIV-1 Protease Inhibitor, Maintains Its Favorable Antiviral Activity against Highly-Drug-Resistant HIV-1 Variants in vitro

Design, synthesis, X-ray studies, and biological evaluation of novel macrocyclic HIV-1 protease inhibitors involving the P1′-P2′ ligands

Design of novel HIV-1 protease inhibitors incorporating isophthalamide-derived P2-P3 ligands: Synthesis, biological evaluation and X-ray structural studies of inhibitor-HIV-1 protease complex

Structure-based design, synthesis, X-ray studies, and biological evaluation of novel HIV-1 protease inhibitors containing isophthalamide-derived P2-ligands

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