S. Meyer

发表

Comparison of LanthaScreen Eu kinase binding assay and surface plasmon resonance method in elucidating the binding kinetics of focal adhesion kinase inhibitors.

Jennifer L. Mason, C. Spais, T. Angeles, 2012, Assay and drug development technologies.

Mutational studies of conserved residues in the dimer interface of nerve growth factor

K. Neet, S. Meyer, M. Guo, 1996, Protein science : a publication of the Protein Society.

A new class of potent vascular endothelial growth factor receptor tyrosine kinase inhibitors: structure-activity relationships for a series of 9-alkoxymethyl-12-(3-hydroxypropyl)indeno[2,1-a]pyrrolo[3,4-c]carbazole-5-ones and the identification of CEP-5214 and its dimethylglycine ester prodrug clini

B. Ruggeri, J. Mallamo, D. Gingrich, 2003, Journal of medicinal chemistry.

Comparison of two homogeneous cell-based kinase assays for JAK2 V617F: SureFire pSTAT5 and GeneBLAzer fluorescence resonance energy transfer assays.

Jennifer L. Mason, J. Qian, T. Angeles, 2012, Assay and drug development technologies.

Anaplastic lymphoma kinase activity is essential for the proliferation and survival of anaplastic large-cell lymphoma cells.

B. Ruggeri, T. Underiner, B. Dorsey, 2006, Blood.

Time-resolved fluorescence resonance energy transfer as a versatile tool in the development of homogeneous cellular kinase assays.

Jennifer L. Mason, C. Spais, T. Angeles, 2012, Assay and drug development technologies.

Biologically active monomeric and heterodimeric recombinant human calpain I produced using the baculovirus expression system.

D. Bozyczko‐Coyne, R. W. Scott, C. Spais, 1996, The Biochemical journal.

Production and Characterization of Recombinant Mouse Brain‐Derived Neurotrophic Factor and Rat Neurotrophin‐3 Expressed in Insect Cells

R. W. Scott, J. Hirsch, R. Scott, 1994, Journal of neurochemistry.

Improvement of inhibitor identification for heat shock protein 90α by utilizing a red-shifted fluorescence polarization probe.

T. Underiner, J. Qian, T. Angeles, 2012, Assay and drug development technologies.

Immunolocalization of caspase proteolysis in situ: evidence for widespread caspase-mediated apoptosis of neurons and glia in the postnatal rat brain

D. Bozyczko‐Coyne, R. Bhat, S. Meyer, 1999, Neuroscience.

A selective, orally bioavailable 1,2,4-triazolo[1,5-a]pyridine-based inhibitor of Janus kinase 2 for use in anticancer therapy: discovery of CEP-33779.

Jennifer L. Mason, Pawel Dobrzanski, Bruce D. Dorsey, 2012, Journal of medicinal chemistry.

Inosine-uridine nucleoside hydrolase from Crithidia fasciculata. Genetic characterization, crystallization, and identification of histidine 241 as a catalytic site residue.

V. Schramm, J. Sacchettini, M. Degano, 1996, Biochemistry.

Subsite requirements for peptide aldehyde inhibitors of human calpain I

Eric C. Griffith, D. Bozyczko‐Coyne, M. Ator, 1997 .

ALK mutants in the kinase domain exhibit altered kinase activity and differential sensitivity to small molecule ALK inhibitors.

A. Ghose, B. Ruggeri, J. T. Durkin, 2009, Biochemistry.

Mixed-lineage kinase 1 and mixed-lineage kinase 3 subtype-selective dihydronaphthyl[3,4-a]pyrrolo[3,4-c]carbazole-5-ones: optimization, mixed-lineage kinase 1 crystallography, and oral in vivo activity in 1-methyl-4-phenyltetrahydropyridine models.

D. Bozyczko‐Coyne, A. Fedorov, E. Fedorov, 2008, Journal of Medicinal Chemistry.

Phosphoregulation of mixed-lineage kinase 1 activity by multiple phosphorylation in the activation loop.

Karla K Kopec, C. Spais, J. T. Durkin, 2004, Biochemistry.

CEP-1347 (KT7515), a Semisynthetic Inhibitor of the Mixed Lineage Kinase Family*

L. Greene, A. Maroney, Zhiheng Xu, 2001, The Journal of Biological Chemistry.

Characterization of AMD, the AMP deaminase gene in yeast. Production of amd strain, cloning, nucleotide sequence, and properties of the protein.

V. Schramm, S. Meyer, K. Kvalnes-Krick, 1989, Biochemistry.

8-THP-DHI analogs as potent Type I dual TIE-2/VEGF-R2 receptor tyrosine kinase inhibitors.

A. Fedorov, E. Fedorov, S. Almo, 2010, Bioorganic & medicinal chemistry letters.

Quantitative non‐radioactive in situ hybridization of preproenkephalin mRNA with digoxigenin‐labeled cRNA probes

M. E. Lewis, J. Roberts-Lewis, S. Meyer, 1991, The Anatomical record.

Successful Identification of Glycine Transporter Inhibitors Using an Adaptation of a Functional Cell-Based Assay

Karla K Kopec, E. Duzic, C. Spais, 2009, Journal of biomolecular screening.

K‐252a and Staurosporine Promote Choline Acetyltransferase Activity in Rat Spinal Cord Cultures

N. Neff, M. Glicksman, S. Meyer, 1993, Journal of neurochemistry.

Aequorin functional assay for characterization of G-protein-coupled receptors: implementation with cryopreserved transiently transfected cells.

E. Duzic, V. Dupriez, M. Ator, 2010, Analytical biochemistry.

Structure and regulation of the AMP nucleosidase gene (amn) from Escherichia coli.

V. Schramm, S. Meyer, K. Kvalnes-Krick, 1989, Biochemistry.

Amino-terminal isoforms of the human glycine transporter GlyT1 exhibit similar pharmacology

Karla K Kopec, C. Spais, J. T. Durkin, 2011, Brain Research.

Modification of CellSensor irf1-bla TF-1 and irf1-bla HEL assays for direct comparison of wild-type JAK2 and JAK2 V617F inhibition.

Jennifer L. Mason, K. Wells-Knecht, T. Angeles, 2011, Assay and drug development technologies.

A sensitive, continuously recording fluorogenic assay for calpain.

D. Bozyczko‐Coyne, R. Siman, M. Ator, 1998, Biochemical and Biophysical Research Communications - BBRC.