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Obesity in Youth with Type 1 Diabetes in Germany, Austria, and the United States

The Journal of pediatrics, 2015-09, Vol.167 (3), p.627-632.e4

2015

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An evaluation of methicillin-resistant Staphylococcus aureus survival on five environmental surfaces

Microbial drug resistance (Larchmont, N.Y.), 2011-09, Vol.17 (3), p.457-461

2011

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1-Aminoindanes as novel motif with potential atypical antipsychotic properties

Bioorganic & medicinal chemistry, 2008-01, Vol.18 (2), p.489-493

2008

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8-Substituted 3,4-dihydroquinolinones as a novel scaffold for atypical antipsychotic activity

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (20), p.4560-4563

2005

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Subtype Selective NMDA Receptor Antagonists: Evaluation of Some Novel Alkynyl Analogues

ChemInform, 2004-06, Vol.35 (23), p.no-no

2004

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Subtype selective NMDA receptor antagonists: evaluation of some novel alkynyl analogues

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (5), p.1213-1216

2004

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Use of trifluoroperazine isolates a [(3)H]Ifenprodil binding site in rat brain membranes with the pharmacology of the voltage-independent ifenprodil site on N-methyl-D-aspartate receptors containing NR2B subunits

The Journal of pharmacology and experimental therapeutics, 2001-01, Vol.296 (1), p.150

2001

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Milameline (CI-979/RU35926): a muscarinic receptor agonist with cognition-activating properties: biochemical and in vivo characterization

The Journal of pharmacology and experimental therapeutics, 1999-11, Vol.291 (2), p.812

1999

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4-Hydroxy-1-[2-(4-hydroxyphenoxy)ethyl]-4-(4-methylbenzyl)piperidine: A Novel, Potent, and Selective NR1/2B NMDA Receptor Antagonist

Journal of medicinal chemistry, 1999-07, Vol.42 (15), p.2993-3000

1999

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Characterization of haloperidol and trifluperidol as subtype-selective N-methyl-D-aspartate (NMDA) receptor antagonists using [3H]TCP and [3H]ifenprodil binding in rat brain membranes

The Journal of pharmacology and experimental therapeutics, 1997-02, Vol.280 (2), p.584

1997

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A specific inhibitor of calcium/calmodulin-dependent protein kinase-II provides neuroprotection against NMDA- and hypoxia/hypoglycemia-induced cell death

The Journal of neuroscience, 1995-05, Vol.15 (5), p.4093-4101

1995

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NS 257 (1,2,3,6,7,8-hexahydro-3(hydroxyimino)-N,N,7-trimethyl-2-oxobenzo[2,1-b:3,4-c']dipyrrole-5-sulfonamide) is a potent, systemically active ampa receptor antagonist

Bioorganic & medicinal chemistry letters, 1994-01, Vol.4 (2), p.371-376

1994

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Synthesis and pharmacological evaluation of 4a-phenanthrenamine derivatives acting at the phencyclidine binding site of the N-methyl-D-aspartate receptor complex

Journal of medicinal chemistry, 1993-07, Vol.36 (14), p.1977-1995

1993

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Synthesis and pharmacological evaluation of hexahydrofluorenamines as noncompetitive antagonists at the N-methyl-D-aspartate receptor

Journal of medicinal chemistry, 1993-03, Vol.36 (6), p.654-670

1993

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Cholinergic Agents: Effect of Methyl Substitution in a Series of Arecoline Derivatives on Binding to Muscarinic Acetylcholine Receptors

Journal of pharmaceutical sciences, 1992-10, Vol.81 (10), p.1015-1019

1992

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Cholinergic agents: aldehyde, ketone, and oxime analogues of the muscarinic agonist UH5

Bioorganic & medicinal chemistry letters, 1992-08, Vol.2 (8), p.803-808

1992

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Exploration of N-phosphonoalkyl-, N-phosphonoalkenyl-, and N-(phosphonoalkyl)phenyl-spaced .alpha.-amino acids as competitive N-methyl-D-aspartic acid antagonists

Journal of medicinal chemistry, 1992-04, Vol.35 (8), p.1371-1384

1992

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Excitatory amino acids: 6-phosphonomethyltetrahydro-4-pyrimidinecarboxylic acids and their acyclic analogues are competitive N-methyl-D-aspartic acid receptor antagonists

Bioorganic & medicinal chemistry letters, 1992, Vol.2 (3), p.207-212

1992

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Cholinergic agents: 2-oxazolidinone analogues of the acetylcholine-receptor muscarinic agonist pilocarpine

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (3), p.147-150

1991

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Structure-activity relationships for enhancement of adenosine A1 receptor binding by 2-amino-3-benzoylthiophenes

Molecular pharmacology, 1990-12, Vol.38 (6), p.950-958

1990

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New and versatile approaches to the synthesis of CPP-related competitive NMDA antagonists. Preliminary structure activity relationships and pharmacological evaluation

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2916-2924

1990

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The Muscarinic Receptors. The Receptors. Joan Heller Brown

The Quarterly review of biology, 1990-09, Vol.65 (3), p.381-381

1990

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Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonists [Erratum to document cited in CA111(3):23931d]

Journal of medicinal chemistry, 1989-12, Vol.32 (12), p.2583-2583

1989

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Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonists

Journal of medicinal chemistry, 1989-07, Vol.32 (7), p.1580-1590

1989

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Alkyl substituted 3-PPP derivatives. Synthesis and biological investigation

Journal of heterocyclic chemistry, 1989-07, Vol.26 (4), p.1125-1128

1989

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Obesity in Youth with Type 1 Diabetes in Germany, Austria, and the United States

An evaluation of methicillin-resistant Staphylococcus aureus survival on five environmental surfaces

1-Aminoindanes as novel motif with potential atypical antipsychotic properties

8-Substituted 3,4-dihydroquinolinones as a novel scaffold for atypical antipsychotic activity

Subtype Selective NMDA Receptor Antagonists: Evaluation of Some Novel Alkynyl Analogues

Subtype selective NMDA receptor antagonists: evaluation of some novel alkynyl analogues

Use of trifluoroperazine isolates a [(3)H]Ifenprodil binding site in rat brain membranes with the pharmacology of the voltage-independent ifenprodil site on N-methyl-D-aspartate receptors containing NR2B subunits

Milameline (CI-979/RU35926): a muscarinic receptor agonist with cognition-activating properties: biochemical and in vivo characterization

4-Hydroxy-1-[2-(4-hydroxyphenoxy)ethyl]-4-(4-methylbenzyl)piperidine: A Novel, Potent, and Selective NR1/2B NMDA Receptor Antagonist

Characterization of haloperidol and trifluperidol as subtype-selective N-methyl-D-aspartate (NMDA) receptor antagonists using [3H]TCP and [3H]ifenprodil binding in rat brain membranes

A specific inhibitor of calcium/calmodulin-dependent protein kinase-II provides neuroprotection against NMDA- and hypoxia/hypoglycemia-induced cell death

NS 257 (1,2,3,6,7,8-hexahydro-3(hydroxyimino)-N,N,7-trimethyl-2-oxobenzo[2,1-b:3,4-c']dipyrrole-5-sulfonamide) is a potent, systemically active ampa receptor antagonist

Synthesis and pharmacological evaluation of 4a-phenanthrenamine derivatives acting at the phencyclidine binding site of the N-methyl-D-aspartate receptor complex

Synthesis and pharmacological evaluation of hexahydrofluorenamines as noncompetitive antagonists at the N-methyl-D-aspartate receptor

Cholinergic Agents: Effect of Methyl Substitution in a Series of Arecoline Derivatives on Binding to Muscarinic Acetylcholine Receptors

Cholinergic agents: aldehyde, ketone, and oxime analogues of the muscarinic agonist UH5

Exploration of N-phosphonoalkyl-, N-phosphonoalkenyl-, and N-(phosphonoalkyl)phenyl-spaced .alpha.-amino acids as competitive N-methyl-D-aspartic acid antagonists

Excitatory amino acids: 6-phosphonomethyltetrahydro-4-pyrimidinecarboxylic acids and their acyclic analogues are competitive N-methyl-D-aspartic acid receptor antagonists

Cholinergic agents: 2-oxazolidinone analogues of the acetylcholine-receptor muscarinic agonist pilocarpine

Structure-activity relationships for enhancement of adenosine A1 receptor binding by 2-amino-3-benzoylthiophenes

New and versatile approaches to the synthesis of CPP-related competitive NMDA antagonists. Preliminary structure activity relationships and pharmacological evaluation

The Muscarinic Receptors. The Receptors. Joan Heller Brown

Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonists [Erratum to document cited in CA111(3):23931d]

Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonists

Alkyl substituted 3-PPP derivatives. Synthesis and biological investigation

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