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Suffruticosol A elevates osteoblast differentiation targeting BMP2‐Smad/1/5/8‐RUNX2 in pre‐osteoblasts

BioFactors (Oxford), 2023-01, Vol.49 (1), p.127-139

2023

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PRDX6 promotes lung tumor progression via its GPx and iPLA2 activities

Free radical biology & medicine, 2014-04, Vol.69, p.367-376

2014

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PRDX6 promotes tumor development via the JAK2/STAT3 pathway in a urethane-induced lung tumor model

Free radical biology & medicine, 2015-03, Vol.80, p.136-144

2015

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G721-0282 inhibits cell growth and induces apoptosis in human osteosarcoma through down-regulation of the STAT3 pathway

International journal of biological sciences, 2020-01, Vol.16 (2), p.330-341

2020

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Peroxiredoxin 6 Inhibits Osteogenic Differentiation and Bone Formation Through Human Dental Pulp Stem Cells and Induces Delayed Bone Development

Antioxidants & redox signaling, 2019-06, Vol.30 (17), p.1969-1982

2019

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Lung tumor growth-promoting function of peroxiredoxin 6

Free radical biology & medicine, 2013-08, Vol.61, p.453-463

2013

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(E)-2,4-Bis(p-hydroxyphenyl)-2-butenal inhibits tumor growth via suppression of NF-κB and induction of death receptor 6

Apoptosis (London), 2014, Vol.19 (1), p.165-178

2014

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Tsg101 Is Essential for Cell Growth, Proliferation, and Cell Survival of Embryonic and Adult Tissues

Molecular and Cellular Biology, 2003-01, Vol.23 (1), p.150-162

2003

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Ox-LDL suppresses PMA-induced MMP-9 expression and activity through CD36-mediated activation of PPAR-γ

Experimental & molecular medicine, 2004-12, Vol.36 (6), p.534-544

2004

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Distinct molecular evolution of influenza H3N2 strains in the 2016/17 season and its implications for vaccine effectiveness

Molecular phylogenetics and evolution, 2019-02, Vol.131, p.29-34

2019

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Design, synthesis, and biological evaluation of novel iso- d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives

Bioorganic & medicinal chemistry, 2007-01, Vol.15 (1), p.227-234

2007

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Asymmetric Synthesis and Biological Activity of l-Bicyclocarba-d4T

Nucleosides, nucleotides & nucleic acids, 2007-01, Vol.26 (10-12), p.1653-1657

2007

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Design, Enantiopure Synthesis, and Biological Evaluation of Novel ISO-D-2′,3′-Dideoxy-3′-Fluorothianucleoside Derivatives as a bioisostere of Lamivudine

Nucleosides, nucleotides & nucleic acids, 2007-01, Vol.26 (8-9), p.911-915

2007

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Synthesis of Enantiopure Pseudo-l-Vinylcyclopropyl Nucleosides Bearing Quaternary Carbon as Potential Anti-Herpesvirus Agent

Nucleosides, nucleotides & nucleic acids, 2007-01, Vol.26 (8-9), p.975-978

2007

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Asymmetric Synthesis of Novel Pseudo-d-Vinylcyclopropyl Nucleosides Bearing Quaternary Carbon as Potential Anti-Herpesvirus Agent

Nucleosides, nucleotides & nucleic acids, 2007-01, Vol.26 (8-9), p.1001-1004

2007

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Asymmetric Synthesis of Apio Fluoroneplanocin a Analogs as Potential AdoHcy Hydrolase Inhibitor

Nucleosides, nucleotides & nucleic acids, 2007-01, Vol.26 (8-9), p.943-947

2007

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Suffruticosol A elevates osteoblast differentiation targeting BMP2‐Smad/1/5/8‐RUNX2 in pre‐osteoblasts

PRDX6 promotes lung tumor progression via its GPx and iPLA2 activities

PRDX6 promotes tumor development via the JAK2/STAT3 pathway in a urethane-induced lung tumor model

G721-0282 inhibits cell growth and induces apoptosis in human osteosarcoma through down-regulation of the STAT3 pathway

Peroxiredoxin 6 Inhibits Osteogenic Differentiation and Bone Formation Through Human Dental Pulp Stem Cells and Induces Delayed Bone Development

Lung tumor growth-promoting function of peroxiredoxin 6

(E)-2,4-Bis(p-hydroxyphenyl)-2-butenal inhibits tumor growth via suppression of NF-κB and induction of death receptor 6

Tsg101 Is Essential for Cell Growth, Proliferation, and Cell Survival of Embryonic and Adult Tissues

Ox-LDL suppresses PMA-induced MMP-9 expression and activity through CD36-mediated activation of PPAR-γ

Distinct molecular evolution of influenza H3N2 strains in the 2016/17 season and its implications for vaccine effectiveness

Design, synthesis, and biological evaluation of novel iso- d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives

Asymmetric Synthesis and Biological Activity of l-Bicyclocarba-d4T

Design, Enantiopure Synthesis, and Biological Evaluation of Novel ISO-D-2′,3′-Dideoxy-3′-Fluorothianucleoside Derivatives as a bioisostere of Lamivudine

Synthesis of Enantiopure Pseudo-l-Vinylcyclopropyl Nucleosides Bearing Quaternary Carbon as Potential Anti-Herpesvirus Agent

Asymmetric Synthesis of Novel Pseudo-d-Vinylcyclopropyl Nucleosides Bearing Quaternary Carbon as Potential Anti-Herpesvirus Agent

Asymmetric Synthesis of Apio Fluoroneplanocin a Analogs as Potential AdoHcy Hydrolase Inhibitor

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