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Impact analysis of human factors on power system operation reliability

Journal of modern power systems and clean energy, 2018, Vol.6 (1), p.27-39

2018

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Pyrazole inhibitors of coactivator associated arginine methyltransferase 1 (CARM1)

Bioorganic & medicinal chemistry, 2008-08, Vol.18 (15), p.4438-4441

2008

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Benzo[ d]imidazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)—Hit to Lead studies

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (17), p.5063-5066

2009

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Optimization of pyrazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)

Bioorganic & medicinal chemistry letters, 2009-06, Vol.19 (11), p.2924-2927

2009

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An electrophoretic mobility shift assay for the identification and kinetic analysis of acetyl transferase inhibitors

Analytical biochemistry, 2010-07, Vol.402 (1), p.65-68

2010

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Blockchain based optimal decision making of dispatchable units in smart grids considering the high uncertainty effects

Sustainable cities and society, 2022-01, Vol.76, p.103418, Article 103418

2022

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Translocation of the Glucose Transporter (GLUT4) to the Cell Surface in Permeabilized 3T3-L1 Adipocytes: Effects of ATP, Insulin, and GTPγS and Localization of GLUT4 to Clathrin Lattices

The Journal of cell biology, 1992-06, Vol.117 (6), p.1181-1196

1992

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Molecular Cloning and Tissue Distribution of PHAS-I, an Intracellular Target for Insulin and Growth Factors

Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3730-3734

1994

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Synthesis and SAR of novel imidazoquinoxaline-Based Lck inhibitors: improvement of cell potency

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (21), p.3153-3156

2002

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GLUT-4 NH2 terminus contains a phenylalanine-based targeting motif that regulates intracellular sequestration

The Journal of cell biology, 1993-06, Vol.121 (6), p.1221-1232

1993

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Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56Lck inhibitors

Bioorganic & medicinal chemistry letters, 2004-12, Vol.14 (24), p.6061-6066

2004

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Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56Lck

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (22), p.4007-4010

2003

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Development and design of dispatcher training simulation evaluation system based on IDAC

2015 IEEE PES Asia-Pacific Power and Energy Engineering Conference (APPEEC), 2015, p.1-5

2015

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Molecular design, synthesis, and structure-activity relationships leading to the potent and selective p56lck inhibitor BMS-243117

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (13), p.2145-2149

2003

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Analysis of power system operation reliability incorporating human errors

2014 17th International Conference on Electrical Machines and Systems (ICEMS), 2014, p.1052-1056

2014

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Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56(lck) inhibitors

Bioorganic & medicinal chemistry letters, 2003-08, Vol.13 (15), p.2587-2590

2003

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The dividing model of islands considering interrupted customers

2012 Power Engineering and Automation Conference, 2012, p.1-5

2012

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Discovery and initial SAR of imidazoquinoxalines as inhibitors of the Src-family kinase p56Lck

Bioorganic & medicinal chemistry letters, 2002-05, Vol.12 (10), p.1361-1364

2002

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Molecular design, synthesis, and structure-Activity relationships leading to the potent and selective p56(lck) inhibitor BMS-243117

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (13), p.2145-2149

2003

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Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56(Lck)

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (22), p.4007-4010

2003

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Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56(Lck) inhibitors

Bioorganic & medicinal chemistry letters, 2004-12, Vol.14 (24), p.6061-6066

2004

Volltextzugriff (PDF)

Discovery and initial SAR of imidazoquinoxalines as inhibitors of the Src-family kinase p56(Lck)

Bioorganic & medicinal chemistry letters, 2002-05, Vol.12 (10), p.1361-1364

2002

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Impact analysis of human factors on power system operation reliability

Pyrazole inhibitors of coactivator associated arginine methyltransferase 1 (CARM1)

Benzo[ d]imidazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)—Hit to Lead studies

Optimization of pyrazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)

An electrophoretic mobility shift assay for the identification and kinetic analysis of acetyl transferase inhibitors

Blockchain based optimal decision making of dispatchable units in smart grids considering the high uncertainty effects

Translocation of the Glucose Transporter (GLUT4) to the Cell Surface in Permeabilized 3T3-L1 Adipocytes: Effects of ATP, Insulin, and GTPγS and Localization of GLUT4 to Clathrin Lattices

Discovery of N-(2-Chloro-6-methyl- phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4- ylamino)thiazole-5-carboxamide (BMS-354825), a Dual Src/Abl Kinase Inhibitor with Potent Antitumor Activity in Preclinical Assays

Molecular Cloning and Tissue Distribution of PHAS-I, an Intracellular Target for Insulin and Growth Factors

Synthesis and SAR of novel imidazoquinoxaline-Based Lck inhibitors: improvement of cell potency

GLUT-4 NH2 terminus contains a phenylalanine-based targeting motif that regulates intracellular sequestration

Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56Lck inhibitors

Imidazoquinoxaline Src-Family Kinase p56Lck Inhibitors: SAR, QSAR, and the Discovery of (S)-N-(2-Chloro-6-methylphenyl)-2-(3-methyl-1-piperazinyl)imidazo- [1,5-a]pyrido[3,2-e]pyrazin-6-amine (BMS-279700) as a Potent and Orally Active Inhibitor with Excellent in Vivo Antiinflammatory Activity

Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56Lck

Development and design of dispatcher training simulation evaluation system based on IDAC

Molecular design, synthesis, and structure-activity relationships leading to the potent and selective p56lck inhibitor BMS-243117

Analysis of power system operation reliability incorporating human errors

Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56(lck) inhibitors

The dividing model of islands considering interrupted customers

Discovery and initial SAR of imidazoquinoxalines as inhibitors of the Src-family kinase p56Lck

Molecular design, synthesis, and structure-Activity relationships leading to the potent and selective p56(lck) inhibitor BMS-243117

Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56(Lck)

Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56(Lck) inhibitors

Discovery and initial SAR of imidazoquinoxalines as inhibitors of the Src-family kinase p56(Lck)

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