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Novel innovative computer-based test (Inno-CBT) item types for national licensing examinations for health care professionals

BMC medical education, 2023-08, Vol.23 (1), p.560-560, Article 560

2023

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A Fully Integrated 0.13-μm CMOS 40-Gb/s Serial Link Transceiver

IEEE journal of solid-state circuits, 2009-05, Vol.44 (5), p.1510-1521

2009

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A novel FGFR1 inhibitor CYY292 suppresses tumor progression, invasion, and metastasis of glioblastoma by inhibiting the Akt/GSK3β/snail signaling axis

Genes & diseases, 2024-01, Vol.11 (1), p.479-494

2024

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Design and Synthesis of l‑1′-Homologated Adenosine Derivatives as Potential Anti-inflammatory Agents

ACS omega, 2023-10, Vol.8 (39), p.36361-36369

2023

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Corrigendum to “A novel FGFR1 inhibitor CYY292 suppresses tumor progression, invasion, and metastasis of glioblastoma by inhibiting the Akt/GSK3β/snail signaling axis” [Genes & Diseases 11 (2024) 479–494]

Genes & diseases, 2024-05, Vol.11 (3), p.101168-101168, Article 101168

2024

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Stereoselective Synthesis of d‑5-Homo-4-selenoribose as a Versatile Intermediate for 4′-Selenonucleosides

Organic letters, 2015-09, Vol.17 (18), p.4636-4639

2015

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Correlation study between A3 adenosine receptor binding affinity and anti-renal interstitial fibrosis activity of truncated adenosine derivatives

Archives of Pharmacal Research, 2019, 42(9), , pp.773-779

2019

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Structure-Activity Relationships of Acyclic Selenopurine Nucleosides as Antiviral Agents

Molecules (Basel, Switzerland), 2017-07, Vol.22 (7), p.1167

2017

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LJ-1888, a selective antagonist for the A 3 adenosine receptor, ameliorates the development of atherosclerosis and hypercholesterolemia in apolipoprotein E knock-out mice

BMB reports, 2018-10, Vol.51 (10), p.520-525

2018

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Synthesis and Anti-HIV Activity of 5′-Homo-2′,3′-dideoxy-2′,3′-didehydro-4′-selenonucleosides (5′-Homo-4′-Se-d4 Ns)

Asian journal of organic chemistry, 2016-06, Vol.5 (6), p.735-741

2016

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Structural basis for activation of fungal sterol receptor Upc2 and azole resistance

Nature chemical biology, 2022-11, Vol.18 (11), p.1253-1262

2022

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Synthesis of Enantiomerically Pure Pyrimidine Ribonucleosides Locked in the South Conformation

Organic letters, 2022-12, Vol.24 (50), p.9281-9284

2022

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A Single-Pair Serial Link for Mobile Displays With Clock Edge Modulation Scheme

IEEE journal of solid-state circuits, 2007-09, Vol.42 (9), p.2012-2020

2007

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Selenoacyclovir and Selenoganciclovir: Discovery of a New Template for Antiviral Agents

Journal of medicinal chemistry, 2015-11, Vol.58 (21), p.8734-8738

2015

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Structural Modification and Biological Evaluation of 2,8-Disubstituted Adenine and Its Nucleosides as A2A Adenosine Receptor Antagonists: Exploring the Roles of Ribose at Adenosine Receptors

Journal of medicinal chemistry, 2024-06, Vol.67 (12), p.10490-10507

2024

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Structural Modification and Biological Evaluation of 2,8-Disubstituted Adenine and Its Nucleosides as A 2A Adenosine Receptor Antagonists: Exploring the Roles of Ribose at Adenosine Receptors

Journal of medicinal chemistry, 2024-06, Vol.67 (12), p.10490-10507

2024

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Asymmetric Total Synthesis of (+)‐Bermudenynol, a C 15 Laurencia Metabolite with a Vinyl Chloride Containing Oxocene Skeleton, through Intramolecular Amide Enolate Alkylation

Angewandte Chemie International Edition, 2014-01, Vol.53 (1), p.272-276

2014

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Discovery and Structure–Activity Relationships of Novel Template, Truncated 1′-Homologated Adenosine Derivatives as Pure Dual PPARγ/δ Modulators

Journal of medicinal chemistry, 2020-12, Vol.63 (24), p.16012-16027

2020

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Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity

Journal of medicinal chemistry, 2023-09, Vol.66 (17), p.12249-12265

2023

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A digital-to-analog converter based on differential-quad switching

IEEE journal of solid-state circuits, 2002-10, Vol.37 (10), p.1335-1338

2002

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GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A 2A Adenosine Receptor

Journal of medicinal chemistry, 2022-09, Vol.65 (17), p.11648-11657

2022

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Design, Synthesis, and Anti-RNA Virus Activity of 6′-Fluorinated-Aristeromycin Analogues

Journal of medicinal chemistry, 2019-07, Vol.62 (13), p.6346-6362

2019

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Correction to "Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A 2A /A 3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity"

Journal of medicinal chemistry, 2024-02, Vol.67 (3), p.2236-2236

2024

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Correction to “Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity”

Journal of medicinal chemistry, 2024-02, Vol.67 (3), p.2236-2236

2024

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Structure–Activity Relationships of Truncated 1′-Homologated Carbaadenosine Derivatives as New PPARγ/δ Ligands: A Study on Sugar Puckering Affecting Binding to PPARs

Journal of medicinal chemistry, 2023-04, Vol.66 (7), p.4961-4978

2023

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Novel innovative computer-based test (Inno-CBT) item types for national licensing examinations for health care professionals

A Fully Integrated 0.13-μm CMOS 40-Gb/s Serial Link Transceiver

A novel FGFR1 inhibitor CYY292 suppresses tumor progression, invasion, and metastasis of glioblastoma by inhibiting the Akt/GSK3β/snail signaling axis

Design and Synthesis of l‑1′-Homologated Adenosine Derivatives as Potential Anti-inflammatory Agents

Corrigendum to “A novel FGFR1 inhibitor CYY292 suppresses tumor progression, invasion, and metastasis of glioblastoma by inhibiting the Akt/GSK3β/snail signaling axis” [Genes & Diseases 11 (2024) 479–494]

Stereoselective Synthesis of d‑5-Homo-4-selenoribose as a Versatile Intermediate for 4′-Selenonucleosides

Correlation study between A3 adenosine receptor binding affinity and anti-renal interstitial fibrosis activity of truncated adenosine derivatives

Structure-Activity Relationships of Acyclic Selenopurine Nucleosides as Antiviral Agents

LJ-1888, a selective antagonist for the A 3 adenosine receptor, ameliorates the development of atherosclerosis and hypercholesterolemia in apolipoprotein E knock-out mice

Synthesis and Anti-HIV Activity of 5′-Homo-2′,3′-dideoxy-2′,3′-didehydro-4′-selenonucleosides (5′-Homo-4′-Se-d4 Ns)

Structural basis for activation of fungal sterol receptor Upc2 and azole resistance

Synthesis of Enantiomerically Pure Pyrimidine Ribonucleosides Locked in the South Conformation

A Single-Pair Serial Link for Mobile Displays With Clock Edge Modulation Scheme

Selenoacyclovir and Selenoganciclovir: Discovery of a New Template for Antiviral Agents

Structural Modification and Biological Evaluation of 2,8-Disubstituted Adenine and Its Nucleosides as A2A Adenosine Receptor Antagonists: Exploring the Roles of Ribose at Adenosine Receptors

Structural Modification and Biological Evaluation of 2,8-Disubstituted Adenine and Its Nucleosides as A 2A Adenosine Receptor Antagonists: Exploring the Roles of Ribose at Adenosine Receptors

Asymmetric Total Synthesis of (+)‐Bermudenynol, a C 15 Laurencia Metabolite with a Vinyl Chloride Containing Oxocene Skeleton, through Intramolecular Amide Enolate Alkylation

Discovery and Structure–Activity Relationships of Novel Template, Truncated 1′-Homologated Adenosine Derivatives as Pure Dual PPARγ/δ Modulators

Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity

A digital-to-analog converter based on differential-quad switching

GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A 2A Adenosine Receptor

Design, Synthesis, and Anti-RNA Virus Activity of 6′-Fluorinated-Aristeromycin Analogues

Correction to "Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A 2A /A 3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity"

Correction to “Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity”

Structure–Activity Relationships of Truncated 1′-Homologated Carbaadenosine Derivatives as New PPARγ/δ Ligands: A Study on Sugar Puckering Affecting Binding to PPARs

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