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Improving γ-ray energy resolution, non-proportionality, and decay time of NaI:Tl+ with Sr2+ and Ca2+ co-doping

Journal of applied physics, 2015-12, Vol.118 (21)

2015

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Design, Synthesis, and Evaluation of Linker-Duocarmycin Payloads: Toward Selection of HER2-Targeting Antibody–Drug Conjugate SYD985

Molecular pharmaceutics, 2015-06, Vol.12 (6), p.1813-1835

2015

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Lanthanum halide scintillators: Properties and applications

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2006-07, Vol.563 (2), p.359-363

2006

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Compaction control and related stress–strain behaviour of off-shore land reclamations with calcareous sands

Soils and foundations, 2015-12, Vol.55 (6), p.1474-1486

2015

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Discovery of SYD5115, a novel orally active small molecule TSH-R antagonist

Bioorganic & medicinal chemistry, 2023-04, Vol.84, p.117258-117258, Article 117258

2023

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Synthesis and Structure−Activity Relationship of the First Nonpeptidergic Inverse Agonists for the Human Cytomegalovirus Encoded Chemokine Receptor US28

Journal of medicinal chemistry, 2005-10, Vol.48 (20), p.6461-6471

2005

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Improvement of γ-ray energy resolution of LaBr3:Ce3+ scintillation detectors by Sr2+ and Ca2+ co-doping

Applied physics letters, 2013-04, Vol.102 (16)

2013

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Isoquinoline and Quinazoline Urea Analogues as Antagonists for the Human Adenosine A3 Receptor

Journal of medicinal chemistry, 2000-06, Vol.43 (11), p.2227-2238

2000

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N-Substituted Piperidinyl Alkyl Imidazoles: Discovery of Methimepip as a Potent and Selective Histamine H3 Receptor Agonist

Journal of medicinal chemistry, 2005-03, Vol.48 (6), p.2100-2107

2005

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Possible Interaction Between Oxcarbazepine and an Oral Contraceptive

Epilepsia (Copenhagen), 1992-11, Vol.33 (6), p.1149-1152

1992

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Synthesis and Structure−Activity Relationships of Conformationally Constrained Histamine H3 Receptor Agonists

Journal of medicinal chemistry, 2003-12, Vol.46 (25), p.5445-5457

2003

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A New Potent and Selective Histamine H3 Receptor Agonist, 4-(1H-imidazol-4-ylmethyl)piperidine

Journal of medicinal chemistry, 1994-02, Vol.37 (3), p.332-333

1994

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Antinociceptive activity of furan-containing congeners of improgan and ranitidine

Bioorganic & medicinal chemistry letters, 2007-10, Vol.17 (20), p.5715-5719

2007

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Development of a Pharmacophore Model for Histamine H3 Receptor Antagonists, Using the Newly Developed Molecular Modeling Program SLATE

Journal of medicinal chemistry, 2001-05, Vol.44 (11), p.1666-1674

2001

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A Chemical Switch for the Modulation of the Functional Activity of Higher Homologues of Histamine on the Human Histamine H3 Receptor: Effect of Various Substitutions at the Primary Amino Function

Journal of medicinal chemistry, 2006-04, Vol.49 (8), p.2549-2557

2006

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Synthesis of Novel Se-Substituted Selenocysteine Derivatives as Potential Kidney Selective Prodrugs of Biologically Active Selenol Compounds: Evaluation of Kinetics of β-Elimination Reactions in Rat Renal Cytosol

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.2040-2046

1996

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Characterization of the Binding Site of the Histamine H3 Receptor. 1. Various Approaches to the Synthesis of 2-(1H-Imidazol-4-yl)cyclopropylamine and Histaminergic Activity of (1R,2R)- and (1S,2S)-2-(1H-Imidazol-4-yl)- cyclopropylamine

Journal of medicinal chemistry, 1999-04, Vol.42 (7), p.1115-1122

1999

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Coupled particle-in-cell and Monte Carlo transport modeling of intense radiographic sources

Journal of applied physics, 2002-03, Vol.91 (5), p.3328-3335

2002

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Homologs of Histamine as Histamine H3 Receptor Antagonists: A New Potent and Selective H3 Antagonist, 4(5)-(5-Aminopentyl)-1H-imidazole

Journal of medicinal chemistry, 1995-01, Vol.38 (2), p.266-271

1995

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Optimization of a rod pinch diode radiography source at 2.3 MV

Review of scientific instruments, 2003-08, Vol.74 (8), p.3628-3635

2003

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Oxcarbazepine Does Not Affect the Anticoagulant Activity of Warfarin

Epilepsia (Copenhagen), 1992-11, Vol.33 (6), p.1145-1148

1992

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Eliminating Fractures in Large Lanthanum Bromide Crystal Packages

IEEE transactions on nuclear science, 2013-04, Vol.60 (2), p.1039-1043

2013

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Behavior of Cs2LiYCl6:Ce scintillator up to 175°C

2011 IEEE Nuclear Science Symposium Conference Record, 2011, p.1598-1601

2011

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Absence of interaction between oxcarbazepine and erythromycin

Acta neurologica Scandinavica, 1992-08, Vol.86 (2), p.120-123

1992

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Improvement of {gamma}-ray energy resolution of LaBr{sub 3}:Ce{sup 3+} scintillation detectors by Sr{sup 2+} and Ca{sup 2+} co-doping

Applied physics letters, 2013-04, Vol.102 (16)

2013

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Improving γ-ray energy resolution, non-proportionality, and decay time of NaI:Tl+ with Sr2+ and Ca2+ co-doping

Design, Synthesis, and Evaluation of Linker-Duocarmycin Payloads: Toward Selection of HER2-Targeting Antibody–Drug Conjugate SYD985

Lanthanum halide scintillators: Properties and applications

Compaction control and related stress–strain behaviour of off-shore land reclamations with calcareous sands

Discovery of SYD5115, a novel orally active small molecule TSH-R antagonist

Synthesis and Structure−Activity Relationship of the First Nonpeptidergic Inverse Agonists for the Human Cytomegalovirus Encoded Chemokine Receptor US28

Improvement of γ-ray energy resolution of LaBr3:Ce3+ scintillation detectors by Sr2+ and Ca2+ co-doping

Isoquinoline and Quinazoline Urea Analogues as Antagonists for the Human Adenosine A3 Receptor

N-Substituted Piperidinyl Alkyl Imidazoles: Discovery of Methimepip as a Potent and Selective Histamine H3 Receptor Agonist

Possible Interaction Between Oxcarbazepine and an Oral Contraceptive

Synthesis and Structure−Activity Relationships of Conformationally Constrained Histamine H3 Receptor Agonists

A New Potent and Selective Histamine H3 Receptor Agonist, 4-(1H-imidazol-4-ylmethyl)piperidine

Antinociceptive activity of furan-containing congeners of improgan and ranitidine

Development of a Pharmacophore Model for Histamine H3 Receptor Antagonists, Using the Newly Developed Molecular Modeling Program SLATE

A Chemical Switch for the Modulation of the Functional Activity of Higher Homologues of Histamine on the Human Histamine H3 Receptor: Effect of Various Substitutions at the Primary Amino Function

Synthesis of Novel Se-Substituted Selenocysteine Derivatives as Potential Kidney Selective Prodrugs of Biologically Active Selenol Compounds: Evaluation of Kinetics of β-Elimination Reactions in Rat Renal Cytosol

Characterization of the Binding Site of the Histamine H3 Receptor. 1. Various Approaches to the Synthesis of 2-(1H-Imidazol-4-yl)cyclopropylamine and Histaminergic Activity of (1R,2R)- and (1S,2S)-2-(1H-Imidazol-4-yl)- cyclopropylamine

Coupled particle-in-cell and Monte Carlo transport modeling of intense radiographic sources

Homologs of Histamine as Histamine H3 Receptor Antagonists: A New Potent and Selective H3 Antagonist, 4(5)-(5-Aminopentyl)-1H-imidazole

Optimization of a rod pinch diode radiography source at 2.3 MV

Oxcarbazepine Does Not Affect the Anticoagulant Activity of Warfarin

Eliminating Fractures in Large Lanthanum Bromide Crystal Packages

Behavior of Cs2LiYCl6:Ce scintillator up to 175°C

Absence of interaction between oxcarbazepine and erythromycin

Improvement of {gamma}-ray energy resolution of LaBr{sub 3}:Ce{sup 3+} scintillation detectors by Sr{sup 2+} and Ca{sup 2+} co-doping

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