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1
Comparison of Changes in Blood Pressure Measurements and Antihypertensive Therapy in Older, Hypertensive, Ambulatory Care Patients Prescribed Celecoxib or Rofecoxib
Comparison of Changes in Blood Pressure Measurements and Antihypertensive Therapy in Older, Hypertensive, Ambulatory Care Patients Prescribed Celecoxib or Rofecoxib
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Comparison of Changes in Blood Pressure Measurements and Antihypertensive Therapy in Older, Hypertensive, Ambulatory Care Patients Prescribed Celecoxib or Rofecoxib

Nietert, Paul J. ; Ornstein, Steven M. ; Dickerson, Lori M. ; Rothenberg, Ralph J.

Pharmacotherapy, 2003-11, Vol.23 (11), p.1416-1423 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Profiles of cognitive dysfunction in chronic amphetamine and heroin abusers
Profiles of cognitive dysfunction in chronic amphetamine and heroin abusers
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Profiles of cognitive dysfunction in chronic amphetamine and heroin abusers

ORNSTEIN, T. J ; IDDON, J. L ; BALDACCHINO, A. M ; SAHAKIAN, B. J ; LONDON, M ; EVERITT, B. J ; ROBBINS, T. W

Neuropsychopharmacology (New York, N.Y.), 2000-08, Vol.23 (2), p.113-126 [Periódico revisado por pares]

New York, NY: Nature Publishing

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3
LY341495 is a nanomolar potent and selective antagonist of group II metabotropic glutamate receptors
LY341495 is a nanomolar potent and selective antagonist of group II metabotropic glutamate receptors
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LY341495 is a nanomolar potent and selective antagonist of group II metabotropic glutamate receptors

Kingston, A.E ; Ornstein, P.L ; Wright, R.A ; Johnson, B.G ; Mayne, N.G ; Burnett, J.P ; Belagaje, R ; Wu, S ; Schoepp, D.D

Neuropharmacology, 1998, Vol.37 (1), p.1-12 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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4
Novel AMPA receptor potentiators LY392098 and LY404187: effects on recombinant human AMPA receptors in vitro
Novel AMPA receptor potentiators LY392098 and LY404187: effects on recombinant human AMPA receptors in vitro
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Novel AMPA receptor potentiators LY392098 and LY404187: effects on recombinant human AMPA receptors in vitro

Miu, P ; Jarvie, K.R ; Radhakrishnan, V ; Gates, M.R ; Ogden, A ; Ornstein, P.L ; Zarrinmayeh, H ; Ho, K ; Peters, D ; Grabell, J ; Gupta, A ; Zimmerman, D.M ; Bleakman, D

Neuropharmacology, 2001-06, Vol.40 (8), p.976-983 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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5
Synthesis and Evaluation of a Series of Novel 2-[(4-Chlorophenoxy)methyl]- benzimidazoles as Selective Neuropeptide Y Y1 Receptor Antagonists
Synthesis and Evaluation of a Series of Novel 2-[(4-Chlorophenoxy)methyl]- benzimidazoles as Selective Neuropeptide Y Y1 Receptor Antagonists
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Synthesis and Evaluation of a Series of Novel 2-[(4-Chlorophenoxy)methyl]- benzimidazoles as Selective Neuropeptide Y Y1 Receptor Antagonists

Zarrinmayeh, Hamideh ; Nunes, Anne M ; Ornstein, Paul L ; Zimmerman, Dennis M ; Arnold, M. Brian ; Schober, Douglas A ; Gackenheimer, Susan L ; Bruns, Robert F ; Hipskind, Philip A ; Britton, Thomas C ; Cantrell, Buddy E ; Gehlert, Donald R

Journal of medicinal chemistry, 1998-07, Vol.41 (15), p.2709-2719 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
Biarylpropylsulfonamides as Novel, Potent Potentiators of 2-Amino-3- (5-methyl-3-hydroxyisoxazol-4-yl)- propanoic Acid (AMPA) Receptors
Biarylpropylsulfonamides as Novel, Potent Potentiators of 2-Amino-3- (5-methyl-3-hydroxyisoxazol-4-yl)- propanoic Acid (AMPA) Receptors
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Biarylpropylsulfonamides as Novel, Potent Potentiators of 2-Amino-3- (5-methyl-3-hydroxyisoxazol-4-yl)- propanoic Acid (AMPA) Receptors

Ornstein, Paul L ; Zimmerman, Dennis M ; Arnold, M. Brian ; Bleisch, Thomas J ; Cantrell, Buddy ; Simon, Richard ; Zarrinmayeh, Hamideh ; Baker, S. Richard ; Gates, Mary ; Tizzano, Joseph P ; Bleakman, David ; Mandelzys, Allan ; Jarvie, Kieth R ; Ho, Ken ; Deverill, Michelle ; Kamboj, Rajender K

Journal of medicinal chemistry, 2000-11, Vol.43 (23), p.4354-4358 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Structure-activity relationship of a series of diaminoalkyl substituted benzimidazole as neuropeptide Y Y1 receptor antagonists
Structure-activity relationship of a series of diaminoalkyl substituted benzimidazole as neuropeptide Y Y1 receptor antagonists
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Structure-activity relationship of a series of diaminoalkyl substituted benzimidazole as neuropeptide Y Y1 receptor antagonists

Zarrinmayeh, Hamideh ; Zimmerman, Dennis M. ; Cantrell, Buddy E. ; Schober, Douglas A. ; Bruns, Robert E. ; Gackenheimer, Susan L. ; Ornstein, Paul L. ; Hipskind, Philip A. ; Britton, Thomas C. ; Gehlert, Donald R.

Bioorganic & medicinal chemistry letters, 1999-03, Vol.9 (5), p.647-652 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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8
2-Substituted (2SR)-2-Amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as Potent and Selective Antagonists of Group II Metabotropic Glutamate Receptors. 2. Effects of Aromatic Substitution, Pharmacological Characterization, and Bioavailability
2-Substituted (2SR)-2-Amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as Potent and Selective Antagonists of Group II Metabotropic Glutamate Receptors. 2. Effects of Aromatic Substitution, Pharmacological Characterization, and Bioavailability
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2-Substituted (2SR)-2-Amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as Potent and Selective Antagonists of Group II Metabotropic Glutamate Receptors. 2. Effects of Aromatic Substitution, Pharmacological Characterization, and Bioavailability

Ornstein, Paul L ; Bleisch, Thomas J ; Arnold, M. Brian ; Kennedy, Joseph H ; Wright, Rebecca A ; Johnson, Bryan G ; Tizzano, Joseph P ; Helton, David R ; Kallman, Mary Jeanne ; Schoepp, Darryle D ; Hérin, Marc

Journal of medicinal chemistry, 1998-01, Vol.41 (3), p.358-378 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
2-Substituted (2SR)-2-Amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as Potent and Selective Antagonists of Group II Metabotropic Glutamate Receptors. 1. Effects of Alkyl, Arylalkyl, and Diarylalkyl Substitution
2-Substituted (2SR)-2-Amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as Potent and Selective Antagonists of Group II Metabotropic Glutamate Receptors. 1. Effects of Alkyl, Arylalkyl, and Diarylalkyl Substitution
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2-Substituted (2SR)-2-Amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as Potent and Selective Antagonists of Group II Metabotropic Glutamate Receptors. 1. Effects of Alkyl, Arylalkyl, and Diarylalkyl Substitution

Ornstein, Paul L ; Bleisch, Thomas J ; Arnold, M. Brian ; Wright, Rebecca A ; Johnson, Bryan G ; Schoepp, Darryle D

Journal of medicinal chemistry, 1998-01, Vol.41 (3), p.346-357 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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10
Synthesis and Structure−Activity Relationships of Novel Arylpiperazines as Potent and Selective Agonists of the Melanocortin Subtype-4 Receptor
Synthesis and Structure−Activity Relationships of Novel Arylpiperazines as Potent and Selective Agonists of the Melanocortin Subtype-4 Receptor
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Synthesis and Structure−Activity Relationships of Novel Arylpiperazines as Potent and Selective Agonists of the Melanocortin Subtype-4 Receptor

Richardson, Timothy I ; Ornstein, Paul L ; Briner, Karin ; Fisher, Matthew J ; Backer, Ryan T ; Biggers, C. Kelly ; Clay, Michael P ; Emmerson, Paul J ; Hertel, Larry W ; Hsiung, Hansen M ; Husain, Saba ; Kahl, Steven D ; Lee, Jonathan A ; Lindstrom, Terry D ; Martinelli, Michael J ; Mayer, John P ; Mullaney, Jeffery T ; O'Brien, Thomas P ; Pawlak, Joseph M ; Revell, Kevin D ; Shah, Jikesh ; Zgombick, John M ; Herr, R. Jason ; Melekhov, Alex ; Sampson, Peter B ; King, Chi-Hsin R

Journal of medicinal chemistry, 2004-01, Vol.47 (3), p.744-755 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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