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The Conformation of the Sarcin/Ricin Loop from 28S Ribosomal RNA

Proceedings of the National Academy of Sciences - PNAS, 1993-10, Vol.90 (20), p.9581-9585

1993

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RNA Tertiary Structure Mediation by Adenosine Platforms

Science (American Association for the Advancement of Science), 1996-09, Vol.273 (5282), p.1696-1699

1996

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Dependencies between Cracking Patterns and the Physico-Mechanical Properties of Microsilica Modified Cement Matrix

IOP conference series. Materials Science and Engineering, 2019-03, Vol.484 (1), p.12015

2019

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Isolation, Structure, and Biological Activities of Fellutamides C and D from an Undescribed Metulocladosporiella (Chaetothyriales) Using the Genome-Wide Candida albicans Fitness Test

Journal of natural products (Washington, D.C.), 2011-08, Vol.74 (8), p.1721-1730

2011

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RESEARCH NOTES: SUMMER HABITAT USE AND HOME-RANGE ANALYSIS OF THE ENDANGERED INDIANA BAT

The Journal of wildlife management, 2005-01, Vol.69 (1), p.430-436

2005

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The Sarcin/Ricin Loop, a Modular RNA

Journal of molecular biology, 1995-03, Vol.247 (1), p.81-98

1995

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SAR profiles of spirocyclic nicotinamide derived selective HDAC1/HDAC2 inhibitors (SHI-1:2)

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (23), p.6104-6109

2008

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The discovery of 6-amino nicotinamides as potent and selective histone deacetylase inhibitors

Bioorganic & medicinal chemistry letters, 2007-10, Vol.17 (19), p.5300-5309

2007

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Discovery of 1-Amino-5H-pyrido[4,3-b]indol-4-carboxamide Inhibitors of Janus Kinase 2 (JAK2) for the Treatment of Myeloproliferative Disorders

Journal of medicinal chemistry, 2011-10, Vol.54 (20), p.7334-7349

2011

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Exploring the pharmacokinetic properties of phosphorus-containing selective HDAC 1 and 2 inhibitors (SHI-1:2)

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (7), p.2053-2058

2009

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Exploration of the internal cavity of histone deacetylase (HDAC) with selective HDAC1/HDAC2 inhibitors (SHI-1:2)

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (3), p.973-978

2008

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Identification of an Active Site Ligand for a Group I Ribozyme Catalytic Metal Ion

Biochemistry (Easton), 2002-02, Vol.41 (8), p.2516-2525

2002

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High-throughput analysis of HGF-stimulated cell scattering

Journal of biomolecular screening, 2008-10, Vol.13 (9), p.847-854

2008

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Genetic and Pharmacological Inhibition of PDK1 in Cancer Cells: CHARACTERIZATION OF A SELECTIVE ALLOSTERIC KINASE INHIBITOR

The Journal of biological chemistry, 2011-02, Vol.286 (8), p.6433-6448

2011

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An RNA internal loop acts as a hinge to facilitate ribozyme folding and catalysis

RNA (Cambridge), 1997-08, Vol.3 (8), p.838-849

1997

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MK-2461, a Novel Multitargeted Kinase Inhibitor, Preferentially Inhibits the Activated c-Met Receptor

Cancer research (Chicago, Ill.), 2010-02, Vol.70 (4), p.1524-1533

2010

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The chemical basis of adenosine conservation throughout the Tetrahymena ribozyme

RNA (Cambridge), 1998-05, Vol.4 (5), p.498-519, Article S1355838298980086

1998

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High-Throughput Quality Control of DMSO Acoustic Dispensing Using Photometric Dye Methods

Journal of Laboratory Automation, 2013-08, Vol.18 (4), p.296-305

2013

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Thermodynamic Stability of the P4−P6 Domain RNA Tertiary Structure Measured by Temperature Gradient Gel Electrophoresis

Biochemistry (Easton), 1998-08, Vol.37 (32), p.11162-11170

1998

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Potent benzoazepinone γ-secretase modulators with improved bioavailability

Bioorganic & medicinal chemistry letters, 2015-09, Vol.25 (17), p.3495-3500

2015

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An Important Base Triple Anchors the Substrate Helix Recognition Surface within the Tetrahymena Ribozyme Active Site

Proceedings of the National Academy of Sciences - PNAS, 1999-09, Vol.96 (20), p.11183-11188

1999

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Microhardness of the slurries and cement mortars

AIP Conference Proceedings, 2018, Vol.2004 (1)

2018

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The Conformation of the Sarcin/Ricin Loop from 28S Ribosomal RNA

RNA Tertiary Structure Mediation by Adenosine Platforms

Dependencies between Cracking Patterns and the Physico-Mechanical Properties of Microsilica Modified Cement Matrix

Isolation, Structure, and Biological Activities of Fellutamides C and D from an Undescribed Metulocladosporiella (Chaetothyriales) Using the Genome-Wide Candida albicans Fitness Test

RESEARCH NOTES: SUMMER HABITAT USE AND HOME-RANGE ANALYSIS OF THE ENDANGERED INDIANA BAT

Efficacious intermittent dosing of a novel JAK2 inhibitor in mouse models of polycythemia vera

The Sarcin/Ricin Loop, a Modular RNA

SAR profiles of spirocyclic nicotinamide derived selective HDAC1/HDAC2 inhibitors (SHI-1:2)

The discovery of 6-amino nicotinamides as potent and selective histone deacetylase inhibitors

Discovery of 1-Amino-5H-pyrido[4,3-b]indol-4-carboxamide Inhibitors of Janus Kinase 2 (JAK2) for the Treatment of Myeloproliferative Disorders

Exploring the pharmacokinetic properties of phosphorus-containing selective HDAC 1 and 2 inhibitors (SHI-1:2)

Exploration of the internal cavity of histone deacetylase (HDAC) with selective HDAC1/HDAC2 inhibitors (SHI-1:2)

Identification of an Active Site Ligand for a Group I Ribozyme Catalytic Metal Ion

High-throughput analysis of HGF-stimulated cell scattering

Genetic and Pharmacological Inhibition of PDK1 in Cancer Cells: CHARACTERIZATION OF A SELECTIVE ALLOSTERIC KINASE INHIBITOR

An RNA internal loop acts as a hinge to facilitate ribozyme folding and catalysis

MK-2461, a Novel Multitargeted Kinase Inhibitor, Preferentially Inhibits the Activated c-Met Receptor

The chemical basis of adenosine conservation throughout the Tetrahymena ribozyme

Discovery of 1‑[3-(1-Methyl‑1H‑pyrazol-4-yl)-5-oxo‑5H‑benzo[4,5]cyclohepta[1,2‑b]pyridin-7-yl]‑N‑(pyridin-2-ylmethyl)methanesulfonamide (MK-8033): A Specific c‑Met/Ron Dual Kinase Inhibitor with Preferential Affinity for the Activated State of c‑Met

Discovery of a 5H-Benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (MK-2461) Inhibitor of c-Met Kinase for the Treatment of Cancer

High-Throughput Quality Control of DMSO Acoustic Dispensing Using Photometric Dye Methods

Thermodynamic Stability of the P4−P6 Domain RNA Tertiary Structure Measured by Temperature Gradient Gel Electrophoresis

Potent benzoazepinone γ-secretase modulators with improved bioavailability

An Important Base Triple Anchors the Substrate Helix Recognition Surface within the Tetrahymena Ribozyme Active Site

Microhardness of the slurries and cement mortars

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