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An Efficient Proteomics Method to Identify the Cellular Targets of Protein Kinase Inhibitors

Proceedings of the National Academy of Sciences - PNAS, 2003-12, Vol.100 (26), p.15434-15439

2003

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Sulfonate Derivatives of Naphtho[2,3-b]thiophen-4(9H)-one and 9(10H)-Anthracenone as Highly Active Antimicrotubule Agents. Synthesis, Antiproliferative Activity, and Inhibition of Tubulin Polymerization

Journal of medicinal chemistry, 2007-11, Vol.50 (24), p.6059-6066

2007

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The Tyrosine Kinase Inhibitor STI571 Induces Cellular Clearance of PrPSc in Prion-infected Cells

The Journal of biological chemistry, 2004-10, Vol.279 (40), p.41918-41927

2004

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Chemical Proteomic Analysis Reveals Alternative Modes of Action for Pyrido[2,3-d]pyrimidine Kinase Inhibitors

Molecular & cellular proteomics, 2004-12, Vol.3 (12), p.1181-1193

2004

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Cell-type specific phosphorylation of threonines T654 and T669 by PKD defines the signal capacity of the EGF receptor

The EMBO journal, 1999-10, Vol.18 (20), p.5567-5576

1999

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Translational potential of the ghrelin receptor agonist macimorelin for seizure suppression in pharmacoresistant epilepsy

European journal of neurology, 2021-09, Vol.28 (9), p.3100-3112

2021

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Trust for Vehicular Applications

Eighth International Symposium on Autonomous Decentralized Systems (ISADS'07), 2007, p.295-304

Gerlach, M.

2007

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Privacy in VANETs using Changing Pseudonyms - Ideal and Real

2007 IEEE 65th Vehicular Technology Conference - VTC2007-Spring, 2007, p.2521-2525

2007

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Whispering gallery modes in photoluminescence and Raman spectra of a spherical microcavity with CdTe quantum dots: anti-Stokes emission and interference effects

Nanoscale research letters, 2006-07, Vol.1 (1), p.68-73

2006

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Abstract 3711: Erk inhibition as a therapeutic option for the treatment of Raf- and Mek- inhibitor resistant tumors

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.3711-3711

2014

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N-Benzoylated Phenoxazines and Phenothiazines: Synthesis, Antiproliferative Activity, and Inhibition of Tubulin Polymerization

Journal of medicinal chemistry, 2011-06, Vol.54 (12), p.4247-4263

2011

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Nanojets and directional emission in symmetric photonic molecules

Optics express, 2007-12, Vol.15 (25), p.17343-17350

2007

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A Convenient Synthesis of Novel 2,8-Disubstituted Pyrido[3,4-b]pyrazines Possessing Biological Activity

Synthesis (Stuttgart), 2012-01, Vol.44 (1), p.69-82

2012

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Preparation of Novel 2,3,8-Trisubstituted Pyrido[3,4-b]pyrazines and Pyrido[2,3-b]pyrazines

Synthesis (Stuttgart), 2011-03, Vol.2011 (5), p.794-806

2011

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Discovery of (7-aryl-1,5-naphthyridin-2-yl)ureas as dual inhibitors of ERK2 and Aurora B kinases with antiproliferative activity against cancer cells

Bioorganic & medicinal chemistry letters, 2014-08, Vol.24 (16), p.3748-3752

2014

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Trustworthy ad hoc communications for intelligent transportation systems - trusted network on wheels

Gerlach, Matthias

2010

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Efficient synthesis of novel disubstituted pyrido[3,4-b]pyrazines for the design of protein kinase inhibitorsElectronic supplementary information (ESI) available: Experimental procedures, previous results of complete pharmacological study of compounds 20a-p. See DOI: 10.1039/c5md00424a

2016-02

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Abstract 871: Dual inhibition of PI3K and Erk1/2 shows synergy and efficacy in human tumor cells, either by using drug combinations or novel dual PI3K/Erk inhibitors

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.871-871

2012

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Both SH2 Domains Are Involved in Interaction of SHP-1 with the Epidermal Growth Factor Receptor but Cannot Confer Receptor-directed Activity to SHP-1/SHP-2 Chimera

The Journal of biological chemistry, 1997-02, Vol.272 (9), p.5966-5973

1997

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Efficient synthesis of novel disubstituted pyrido[3,4-b]pyrazines for the design of protein kinase inhibitors

MedChemComm, 2016-01, Vol.7 (2), p.224-229

2016

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Radiation-pressure-induced mode splitting in a spherical microcavity with an elastic shell

Optics express, 2007-03, Vol.15 (6), p.3597-3606

2007

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Abstract 5476: LHRH receptor targeting as mechanism of anti-tumor activity for cytotoxic conjugates of Disorazol Z with the LHRH receptor agonistic peptide D-Lys6-LHRH

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.5476-5476

2013

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Abstract 3563: A highly selective Erk1/2 Inhibitor with in-vivo anti tumor potency

Cancer research (Chicago, Ill.), 2011-04, Vol.71 (8_Supplement), p.3563-3563

2011

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Discovery of 7-Aryl-Substituted (1,5-Naphthyridin-4-yl)ureas as Aurora Kinase Inhibitors

ChemMedChem, 2014-01, Vol.9 (1), p.217-232

2014

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Phenylimino-10H-anthracen-9-ones as novel antimicrotubule agents—synthesis, antiproliferative activity and inhibition of tubulin polymerization

Bioorganic & medicinal chemistry, 2011-07, Vol.19 (14), p.4183-4191

2011

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An Efficient Proteomics Method to Identify the Cellular Targets of Protein Kinase Inhibitors

Sulfonate Derivatives of Naphtho[2,3-b]thiophen-4(9H)-one and 9(10H)-Anthracenone as Highly Active Antimicrotubule Agents. Synthesis, Antiproliferative Activity, and Inhibition of Tubulin Polymerization

The Tyrosine Kinase Inhibitor STI571 Induces Cellular Clearance of PrPSc in Prion-infected Cells

Chemical Proteomic Analysis Reveals Alternative Modes of Action for Pyrido[2,3-d]pyrimidine Kinase Inhibitors

Cell-type specific phosphorylation of threonines T654 and T669 by PKD defines the signal capacity of the EGF receptor

Translational potential of the ghrelin receptor agonist macimorelin for seizure suppression in pharmacoresistant epilepsy

Trust for Vehicular Applications

Privacy in VANETs using Changing Pseudonyms - Ideal and Real

Whispering gallery modes in photoluminescence and Raman spectra of a spherical microcavity with CdTe quantum dots: anti-Stokes emission and interference effects

Abstract 3711: Erk inhibition as a therapeutic option for the treatment of Raf- and Mek- inhibitor resistant tumors

N-Benzoylated Phenoxazines and Phenothiazines: Synthesis, Antiproliferative Activity, and Inhibition of Tubulin Polymerization

Nanojets and directional emission in symmetric photonic molecules

A Convenient Synthesis of Novel 2,8-Disubstituted Pyrido[3,4-b]pyrazines Possessing Biological Activity

Preparation of Novel 2,3,8-Trisubstituted Pyrido[3,4-b]pyrazines and Pyrido[2,3-b]pyrazines

Discovery of (7-aryl-1,5-naphthyridin-2-yl)ureas as dual inhibitors of ERK2 and Aurora B kinases with antiproliferative activity against cancer cells

Trustworthy ad hoc communications for intelligent transportation systems - trusted network on wheels

Efficient synthesis of novel disubstituted pyrido[3,4-b]pyrazines for the design of protein kinase inhibitorsElectronic supplementary information (ESI) available: Experimental procedures, previous results of complete pharmacological study of compounds 20a-p. See DOI: 10.1039/c5md00424a

Abstract 871: Dual inhibition of PI3K and Erk1/2 shows synergy and efficacy in human tumor cells, either by using drug combinations or novel dual PI3K/Erk inhibitors

Both SH2 Domains Are Involved in Interaction of SHP-1 with the Epidermal Growth Factor Receptor but Cannot Confer Receptor-directed Activity to SHP-1/SHP-2 Chimera

Efficient synthesis of novel disubstituted pyrido[3,4-b]pyrazines for the design of protein kinase inhibitors

Radiation-pressure-induced mode splitting in a spherical microcavity with an elastic shell

Abstract 5476: LHRH receptor targeting as mechanism of anti-tumor activity for cytotoxic conjugates of Disorazol Z with the LHRH receptor agonistic peptide D-Lys6-LHRH

Abstract 3563: A highly selective Erk1/2 Inhibitor with in-vivo anti tumor potency

Discovery of 7-Aryl-Substituted (1,5-Naphthyridin-4-yl)ureas as Aurora Kinase Inhibitors

Phenylimino-10H-anthracen-9-ones as novel antimicrotubule agents—synthesis, antiproliferative activity and inhibition of tubulin polymerization

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