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Quantitation of doxorubicin uptake, efflux, and modulation of multidrug resistance (MDR) in MDR human cancer cells

The Journal of pharmacology and experimental therapeutics, 2008-01, Vol.324 (1), p.95-102

2008

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Dynamic assessment of mitoxantrone resistance and modulation of multidrug resistance by valspodar (PSC833) in multidrug resistance human cancer cells

The Journal of pharmacology and experimental therapeutics, 2009-08, Vol.330 (2), p.423-429

2009

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A Phase 1b trial of prexasertib in combination with chemoradiation in patients with locally advanced head and neck squamous cell carcinoma

Radiotherapy and oncology, 2021-04, Vol.157, p.203-209

2021

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Phase I pharmacokinetic studies evaluating single and multiple doses of oral GW572016, a dual EGFR-ErbB2 inhibitor, in healthy subjects

Investigational new drugs, 2005-01, Vol.23 (1), p.39-49

2005

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In vivo evaluation of diaminodiphenyls: Anticonvulsant agents with minimal acute neurotoxicity

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (17), p.5012-5015

2009

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An in vivo evaluation of the antiseizure activity and acute neurotoxicity of agmatine

Pharmacology, biochemistry and behavior, 2003-02, Vol.74 (3), p.771-775

2003

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The Mechanism of l-Canavanine Cytotoxicity: Arginyl tRNA Synthetase as a Novel Target for Anticancer Drug Discovery

Journal of enzyme inhibition and medicinal chemistry, 2003-10, Vol.18 (5), p.383-394

2003

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Aminoanthraquinones as novel ligands at the polyamine binding site on the N-methyl- d-aspartate receptor complex

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (23), p.2621-2623

2000

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L-Canavanine as a radiosensitization agent for human pancreatic cancer cells

Molecular and cellular biochemistry, 2003-02, Vol.244 (1-2), p.37-43

2003

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The antiproliferative and immunotoxic effects of L-canavanine and L-canaline

Anti-cancer drugs, 2002-03, Vol.13 (3), p.313-320

2002

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Endogenous indoles as novel polyamine site ligands at the N-methyl- d-aspartate receptor complex

Brain research, 2001-02, Vol.890 (2), p.343-346

2001

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Abstract LB-200: Dose and schedule determination of the Chk1/2 inhibitor LY2606368 in patients with solid tumors

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.LB-200-LB-200

2013

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Abstract A108: LY2606368, a second generation Chk1 inhibitor, inhibits growth of ovarian carcinoma xenografts either as monotherapy or in combination with standard-of-care agents

Molecular cancer therapeutics, 2011-11, Vol.10 (11_Supplement), p.A108-A108

2011

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Abstract 1776: Antitumor activity of Chk1 inhibitor LY2606368 as a single agent in SW1990 human pancreas orthotopic tumor model

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.1776-1776

2012

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Dapsone analogs as potential polyamine binding site modulators of the N-methyl-D-aspartate receptor complex

Drug development research, 2000-12, Vol.51 (4), p.268-272

2000

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Pegfilgrastim: A New Therapy to Prevent Neutropenic Fever

Journal of the American Pharmaceutical Association (1996), 2002-09, Vol.42 (5), p.806-808

2002

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SYNTHESIS OF L-INDOSPICINE

Synthetic communications, 2002-01, Vol.32 (13), p.2075-2082

2002

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Synthesis of L-Indospicine

ChemInform, 2002-12, Vol.33 (48), p.191-191

2002

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Antiangiogenesis Agents in Clinical Trials

Journal of the American Pharmaceutical Association (1961), 2001-11, Vol.41 (6), p.893-895

2001

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Antiangiogenesis Agents in Clinical Trials

Journal of the American Pharmaceutical Association (1996), 2001-11, Vol.41 (6), p.893-895

2001

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ChemInform Abstract: Aminoanthraquinones as Novel Ligands at the Polyamine Binding Site on the N-Methyl-D-aspartate Receptor Complex

ChemInform, 2001-04, Vol.32 (14), p.no-no

2001

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Therapeutic high affinity T cell receptor targeting a KRASG12D cancer neoantigen

Nature communications, 2022-09, Vol.13 (1), p.5333-15, Article 5333

2022

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Phase III study of selpercatinib versus chemotherapy ± pembrolizumab in untreated RET positive non-small-cell lung cancer

Future oncology (London, England), 2021-03, Vol.17 (7), p.763-773

2021

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Quantitation of doxorubicin uptake, efflux, and modulation of multidrug resistance (MDR) in MDR human cancer cells

Dynamic assessment of mitoxantrone resistance and modulation of multidrug resistance by valspodar (PSC833) in multidrug resistance human cancer cells

A Phase 1b trial of prexasertib in combination with chemoradiation in patients with locally advanced head and neck squamous cell carcinoma

Phase I pharmacokinetic studies evaluating single and multiple doses of oral GW572016, a dual EGFR-ErbB2 inhibitor, in healthy subjects

In vivo evaluation of diaminodiphenyls: Anticonvulsant agents with minimal acute neurotoxicity

An in vivo evaluation of the antiseizure activity and acute neurotoxicity of agmatine

The Mechanism of l-Canavanine Cytotoxicity: Arginyl tRNA Synthetase as a Novel Target for Anticancer Drug Discovery

Aminoanthraquinones as novel ligands at the polyamine binding site on the N-methyl- d-aspartate receptor complex

L-Canavanine as a radiosensitization agent for human pancreatic cancer cells

The antiproliferative and immunotoxic effects of L-canavanine and L-canaline

Endogenous indoles as novel polyamine site ligands at the N-methyl- d-aspartate receptor complex

Abstract LB-200: Dose and schedule determination of the Chk1/2 inhibitor LY2606368 in patients with solid tumors

Abstract A108: LY2606368, a second generation Chk1 inhibitor, inhibits growth of ovarian carcinoma xenografts either as monotherapy or in combination with standard-of-care agents

Abstract 1776: Antitumor activity of Chk1 inhibitor LY2606368 as a single agent in SW1990 human pancreas orthotopic tumor model

Dapsone analogs as potential polyamine binding site modulators of the N-methyl-D-aspartate receptor complex

Pegfilgrastim: A New Therapy to Prevent Neutropenic Fever

SYNTHESIS OF L-INDOSPICINE

Synthesis of L-Indospicine

Antiangiogenesis Agents in Clinical Trials

Antiangiogenesis Agents in Clinical Trials

ChemInform Abstract: Aminoanthraquinones as Novel Ligands at the Polyamine Binding Site on the N-Methyl-D-aspartate Receptor Complex

Therapeutic high affinity T cell receptor targeting a KRASG12D cancer neoantigen

Broad Spectrum Activity of the Checkpoint Kinase 1 Inhibitor Prexasertib as a Single Agent or Chemopotentiator Across a Range of Preclinical Pediatric Tumor Models

Current operative management of congenital lobar emphysema in children: A report from the Midwest Pediatric Surgery Consortium

Phase III study of selpercatinib versus chemotherapy ± pembrolizumab in untreated RET positive non-small-cell lung cancer

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