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Pain Prevalence and Trajectories Following Pediatric Spinal Fusion Surgery

The journal of pain, 2013-12, Vol.14 (12), p.1694-1702

2013

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Rational Design of Potent Non-Nucleoside Inhibitors of HIV‑1 Reverse Transcriptase

Journal of medicinal chemistry, 2012-12, Vol.55 (23), p.10601-10609

2012

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Pain Outcomes in Patients Undergoing CT-Guided Celiac Plexus Neurolysis for Intractable Abdominal Visceral Pain

American journal of hospice & palliative medicine, 2017-03, Vol.34 (2), p.111-114

2017

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Blockade of X4-Tropic HIV-1 Cellular Entry by GSK812397, a Potent Noncompetitive CXCR4 Receptor Antagonist

Antimicrobial Agents and Chemotherapy, 2010-02, Vol.54 (2), p.817-824

2010

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The relative activity of "function sparing" HIV-1 entry inhibitors on viral entry and CCR5 internalization: is allosteric functional selectivity a valuable therapeutic property?

Molecular pharmacology, 2009-03, Vol.75 (3), p.490-501

2009

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Synthesis and evaluation of 2-phenyl-1,4-butanediamine-based CCR5 antagonists for the treatment of HIV-1

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (5), p.1394-1398

2011

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Ultrasonography-Guided Procedures in the Intensive Care Setting

AACN advanced critical care, 2023-09, Vol.34 (3), p.201-206

2023

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Marriage Dissolution in the Active Duty Air Force

Edelstein, Mark

2017

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Oxindole-Based Inhibitors of Cyclin-Dependent Kinase 2 (CDK2): Design, Synthesis, Enzymatic Activities, and X-ray Crystallographic Analysis

Journal of medicinal chemistry, 2001-12, Vol.44 (25), p.4339-4358

2001

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Discovery of a novel series of cyclic urea as potent CCR5 antagonists

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6381-6385

2011

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Discovery of N-benzyl- N′-(4-pipyridinyl)urea CCR5 antagonists as anti-HIV-1 agents (I): Optimization of the amine portion

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (24), p.7397-7400

2010

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Discovery of novel pyridyl carboxamides as potent CCR5 antagonists and optimization of their pharmacokinetic profile in rats

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6470-6475

2011

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Discovery of N-benzyl- N′-(4-pipyridinyl)urea CCR5 antagonists as anti-HIV-1 agents (II): Modification of the acyl portion

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (24), p.7401-7404

2010

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Prevention of Chemotherapy-Induced Alopecia in Rats by CDK Inhibitors

Science (American Association for the Advancement of Science), 2001-01, Vol.291 (5501), p.134-137

2001

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Induction of apoptosis of human B-CLL and ALL cells by a novel retinoid and its nonretinoidal analog

Blood, 2002-10, Vol.100 (8), p.2917-2925

2002

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Synthesis and biological activity of an acyclic analog of 5,6,7,8-tetrahydrofolic acid, N-[4-[[3-(2,4-diamino-1,6-dihydro-6-oxo-5-pyrimidinyl)propyl]amino]benzoyl]-L-glutamic acid

Journal of medicinal chemistry, 1990-02, Vol.33 (2), p.561-567

1990

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The actions of interferon and antiinflammatory agents on induction of indoleamine 2,3-dioxygenase in human peripheral blood monocytes

Biochemical and biophysical research communications, 1987-05, Vol.144 (3), p.1147-1153

1987

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Induction of Indoleamine 2,3-dioxygenase: A Mechanism of the Antitumor Activity of Interferon γ

Proceedings of the National Academy of Sciences - PNAS, 1988-02, Vol.85 (4), p.1242-1246

1988

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Induction of apoptosis in retinoid-refractory acute myelogenous leukemia by a novel AHPN analog

Blood, 2003-11, Vol.102 (10), p.3743-3752

2003

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Biochemical and chemotherapeutic studies on 2,4-diamino-6-(2,5-dimethoxybenzyl)-5-methylpyrido[2,3-d]pyrimidine (BW 301U), a novel lipid-soluble inhibitor of dihydrofolate reductase

Cancer research (Chicago, Ill.), 1982-10, Vol.42 (10), p.3987-3994

1982

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Specificity, schedule, and proliferation dependence of infused L-histidinol after 5-fluorouracil in mice

Cancer research (Chicago, Ill.), 1988-03, Vol.48 (6), p.1470-1475

1988

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Unusual case of antiphospholipid antibody syndrome presenting with extensive cutaneous infarcts in a patient on long‐term procainamide therapy

American journal of hematology, 2003-02, Vol.72 (2), p.154-154

2003

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Hemorrhagic ascites due to congestive heart failure

The American journal of gastroenterology, 1998, Vol.93 (7), p.1176-1177

1998

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Synthesis and biological activity of an acyclic analog of 5,6,7,8-tetrahydrofolic acid, N-[4-[[3-(2,4-diamino-1,6-dihydro-6-oxo-5-pyrimidinyl)propyl]amino]benzoyl]-L-glutamic acid [Erratum to document cited in CA112(7):56616d]

Journal of medicinal chemistry, 1990-11, Vol.33 (11), p.3116-3116

1990

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The Relative Activity of âFunction Sparingâ HIV-1 Entry Inhibitors on Viral Entry and CCR5 Internalization: Is Allosteric Functional Selectivity a Valuable Therapeutic Property?

Molecular pharmacology, 2009-03, Vol.75 (3), p.490

2009

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Pain Prevalence and Trajectories Following Pediatric Spinal Fusion Surgery

Rational Design of Potent Non-Nucleoside Inhibitors of HIV‑1 Reverse Transcriptase

Pain Outcomes in Patients Undergoing CT-Guided Celiac Plexus Neurolysis for Intractable Abdominal Visceral Pain

Blockade of X4-Tropic HIV-1 Cellular Entry by GSK812397, a Potent Noncompetitive CXCR4 Receptor Antagonist

The relative activity of "function sparing" HIV-1 entry inhibitors on viral entry and CCR5 internalization: is allosteric functional selectivity a valuable therapeutic property?

Synthesis and evaluation of 2-phenyl-1,4-butanediamine-based CCR5 antagonists for the treatment of HIV-1

Ultrasonography-Guided Procedures in the Intensive Care Setting

Marriage Dissolution in the Active Duty Air Force

Oxindole-Based Inhibitors of Cyclin-Dependent Kinase 2 (CDK2): Design, Synthesis, Enzymatic Activities, and X-ray Crystallographic Analysis

Discovery of a novel series of cyclic urea as potent CCR5 antagonists

Discovery of N-benzyl- N′-(4-pipyridinyl)urea CCR5 antagonists as anti-HIV-1 agents (I): Optimization of the amine portion

Discovery of novel pyridyl carboxamides as potent CCR5 antagonists and optimization of their pharmacokinetic profile in rats

Discovery of N-benzyl- N′-(4-pipyridinyl)urea CCR5 antagonists as anti-HIV-1 agents (II): Modification of the acyl portion

Prevention of Chemotherapy-Induced Alopecia in Rats by CDK Inhibitors

Induction of apoptosis of human B-CLL and ALL cells by a novel retinoid and its nonretinoidal analog

Synthesis and biological activity of an acyclic analog of 5,6,7,8-tetrahydrofolic acid, N-[4-[[3-(2,4-diamino-1,6-dihydro-6-oxo-5-pyrimidinyl)propyl]amino]benzoyl]-L-glutamic acid

The actions of interferon and antiinflammatory agents on induction of indoleamine 2,3-dioxygenase in human peripheral blood monocytes

Induction of Indoleamine 2,3-dioxygenase: A Mechanism of the Antitumor Activity of Interferon γ

Induction of apoptosis in retinoid-refractory acute myelogenous leukemia by a novel AHPN analog

Biochemical and chemotherapeutic studies on 2,4-diamino-6-(2,5-dimethoxybenzyl)-5-methylpyrido[2,3-d]pyrimidine (BW 301U), a novel lipid-soluble inhibitor of dihydrofolate reductase

Specificity, schedule, and proliferation dependence of infused L-histidinol after 5-fluorouracil in mice

Unusual case of antiphospholipid antibody syndrome presenting with extensive cutaneous infarcts in a patient on long‐term procainamide therapy

Hemorrhagic ascites due to congestive heart failure

Synthesis and biological activity of an acyclic analog of 5,6,7,8-tetrahydrofolic acid, N-[4-[[3-(2,4-diamino-1,6-dihydro-6-oxo-5-pyrimidinyl)propyl]amino]benzoyl]-L-glutamic acid [Erratum to document cited in CA112(7):56616d]

The Relative Activity of âFunction Sparingâ HIV-1 Entry Inhibitors on Viral Entry and CCR5 Internalization: Is Allosteric Functional Selectivity a Valuable Therapeutic Property?

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