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Single nucleotide polymorphisms in fibroblast growth factor 23 gene, FGF23, are associated with prostate cancer risk

BJU international, 2014-08, Vol.114 (2), p.303-310

2014

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Expression of the Discoidin Domain Receptor Family Depended on Glucose and Their High Expression in Arterial Tissues in the Rat Model of Type 2 Diabetes

Biological and Pharmaceutical Bulletin, 2024/07/13, Vol.47(7), pp.1288-1295

2024

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Adiponectin induces growth arrest and apoptosis of MDA-MB-231 breast cancer cell

Archives of Pharmacal Research, 2005, 28(11), , pp.1263-1269

2005

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Anti-angiogenic activity of thienopyridine derivative LCB03-0110 by targeting VEGFR-2 and JAK/STAT3 Signalling

Experimental dermatology, 2015-07, Vol.24 (7), p.503-509

2015

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Topical application of ALK5 inhibitor A-83-01 reduces burn wound contraction in rats by suppressing myofibroblast population

Bioscience, biotechnology, and biochemistry, 2014-11, Vol.78 (11), p.1805-1812

2014

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Low Stability and a Conserved N-Glycosylation Site Are Associated with Regulation of the Discoidin Domain Receptor Family by Glucose via Post-Translational N-Glycosylation

Bioscience, biotechnology, and biochemistry, 2013, Vol.77 (9), p.1907-1916

2013

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Tyrosine 740 Phosphorylation of Discoidin Domain Receptor 2 by Src Stimulates Intramolecular Autophosphorylation and Shc Signaling Complex Formation

The Journal of biological chemistry, 2005-11, Vol.280 (47), p.39058-39066

2005

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Actinomycin D Identified as an Inhibitor of Discoidin Domain Receptor 2 Interaction with Collagen through an Insect Cell Based Screening of a Drug Compound Library

Biological and Pharmaceutical Bulletin, 2009/01/01, Vol.32(1), pp.136-141

2009

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Quercetin Shows the Pharmacological Activity to Simultaneously Downregulate the Inflammatory and Fibrotic Responses to Tissue Injury in Association with its Ability to Target Multi-Kinases

Pharmacology, 2018-01, Vol.102 (3-4), p.142-153

2018

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Ras-mediated phosphorylation of a conserved threonine residue enhances the transactivation activities of c-Ets1 and c-Ets2

Molecular and Cellular Biology, 1996-02, Vol.16 (2), p.538-547

1996

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LCB 03-0110, a novel pan-discoidin domain receptor/c-Src family tyrosine kinase inhibitor, suppresses scar formation by inhibiting fibroblast and macrophage activation

The Journal of pharmacology and experimental therapeutics, 2012-03, Vol.340 (3), p.510-519

2012

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Defective Ca(2+) binding in a conserved binding site causes incomplete N-glycan processing and endoplasmic reticulum trapping of discoidin domain receptors

Bioscience, biotechnology, and biochemistry, 2015, Vol.79 (4), p.574-580

2015

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Defective Ca2+ binding in a conserved binding site causes incomplete N-glycan processing and endoplasmic reticulum trapping of discoidin domain receptors

Bioscience, biotechnology, and biochemistry, 2015-04, Vol.79 (4), p.574-580

2015

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Synthesis and biological evaluations of pyrazolo[3,4- d]pyrimidines as cyclin-dependent kinase 2 inhibitors

European journal of medicinal chemistry, 2003-05, Vol.38 (5), p.525-532

2003

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Topical Administration of Manuka Oil Prevents UV-B Irradiation-Induced Cutaneous Photoaging in Mice

Evidence-based complementary and alternative medicine, 2013-01, Vol.2013 (2013), p.1-10

2013

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N′-(phenyl-pyridin-2-yl-methylene)-hydrazine carbodithioic acid methyl ester enhances radiation-induced cell death by targeting Bcl-2 against human lung carcinoma cells

Molecular cancer therapeutics, 2004-04, Vol.3 (4), p.403-407

2004

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Synthesis and Biological Evaluation of Bis(methoxy methyl)-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolines as EGFR Tyrosine Kinase Inhibitors

Archiv der Pharmazie (Weinheim), 2005-10, Vol.338 (10), p.502-505

2005

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Rapid phosphorylation of Ets-2 accompanies mitogen-activated protein kinase activation and the induction of heparin-binding epidermal growth factor gene expression by oncogenic Raf-1

Molecular and Cellular Biology, 1997-05, Vol.17 (5), p.2401-2412

1997

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1,4-Dioxane-fused 4-anilinoquinazoline as inhibitors of epidermal growth factor receptor kinase

Archiv der Pharmazie (Weinheim), 2001-12, Vol.334 (11), p.357-360

2001

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7-Substituted-[1, 4]dioxano[2, 3-g]quinazolines as Inhibitors of Epidermal Growth Factor Receptor Kinase

Archiv der Pharmazie (Weinheim), 2002-12, Vol.335 (10), p.487-494

2002

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Overexpression of Myc suppresses CCAAT transcription factor/nuclear factor 1-dependent promoters in vivo

Molecular and Cellular Biology, 1993-05, Vol.13 (5), p.3093-3102

1993

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Effects of Sr on the Characteristics of PZT Ceramics Prepared by Hydrothermal Process

한국세라믹학회지, 2008, 45(11), 318, pp.681-687

2008

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Effects of Sr on the Electrical Properties of PZT Ceramics Prepared by Self-propagating High-temperature Synthesis

한국세라믹학회지, 2008, 45(11), 318, pp.713-718

2008

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Synthesis and Biological Evaluation of Furo[2,3-d]pyrimidines as Akt1 Kinase Inhibitors

Bulletin of the Korean Chemical Society, 2007, 28(7), , pp.1114-1118

2007

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QM and Pharmacophore based 3D-QSAR of MK886 Analogues against mPGES-1

Bulletin of the Korean Chemical Society, 2008, 29(3), , pp.647-655

2008

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Single nucleotide polymorphisms in fibroblast growth factor 23 gene, FGF23, are associated with prostate cancer risk

Expression of the Discoidin Domain Receptor Family Depended on Glucose and Their High Expression in Arterial Tissues in the Rat Model of Type 2 Diabetes

Adiponectin induces growth arrest and apoptosis of MDA-MB-231 breast cancer cell

Anti-angiogenic activity of thienopyridine derivative LCB03-0110 by targeting VEGFR-2 and JAK/STAT3 Signalling

Topical application of ALK5 inhibitor A-83-01 reduces burn wound contraction in rats by suppressing myofibroblast population

Low Stability and a Conserved N-Glycosylation Site Are Associated with Regulation of the Discoidin Domain Receptor Family by Glucose via Post-Translational N-Glycosylation

Tyrosine 740 Phosphorylation of Discoidin Domain Receptor 2 by Src Stimulates Intramolecular Autophosphorylation and Shc Signaling Complex Formation

Actinomycin D Identified as an Inhibitor of Discoidin Domain Receptor 2 Interaction with Collagen through an Insect Cell Based Screening of a Drug Compound Library

Quercetin Shows the Pharmacological Activity to Simultaneously Downregulate the Inflammatory and Fibrotic Responses to Tissue Injury in Association with its Ability to Target Multi-Kinases

Ras-mediated phosphorylation of a conserved threonine residue enhances the transactivation activities of c-Ets1 and c-Ets2

LCB 03-0110, a novel pan-discoidin domain receptor/c-Src family tyrosine kinase inhibitor, suppresses scar formation by inhibiting fibroblast and macrophage activation

Defective Ca(2+) binding in a conserved binding site causes incomplete N-glycan processing and endoplasmic reticulum trapping of discoidin domain receptors

Defective Ca2+ binding in a conserved binding site causes incomplete N-glycan processing and endoplasmic reticulum trapping of discoidin domain receptors

Synthesis and biological evaluations of pyrazolo[3,4- d]pyrimidines as cyclin-dependent kinase 2 inhibitors

Topical Administration of Manuka Oil Prevents UV-B Irradiation-Induced Cutaneous Photoaging in Mice

N′-(phenyl-pyridin-2-yl-methylene)-hydrazine carbodithioic acid methyl ester enhances radiation-induced cell death by targeting Bcl-2 against human lung carcinoma cells

Synthesis and Biological Evaluation of Bis(methoxy methyl)-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolines as EGFR Tyrosine Kinase Inhibitors

Rapid phosphorylation of Ets-2 accompanies mitogen-activated protein kinase activation and the induction of heparin-binding epidermal growth factor gene expression by oncogenic Raf-1

1,4-Dioxane-fused 4-anilinoquinazoline as inhibitors of epidermal growth factor receptor kinase

7-Substituted-[1, 4]dioxano[2, 3-g]quinazolines as Inhibitors of Epidermal Growth Factor Receptor Kinase

Overexpression of Myc suppresses CCAAT transcription factor/nuclear factor 1-dependent promoters in vivo

Effects of Sr on the Characteristics of PZT Ceramics Prepared by Hydrothermal Process

Effects of Sr on the Electrical Properties of PZT Ceramics Prepared by Self-propagating High-temperature Synthesis

Synthesis and Biological Evaluation of Furo[2,3-d]pyrimidines as Akt1 Kinase Inhibitors

QM and Pharmacophore based 3D-QSAR of MK886 Analogues against mPGES-1

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