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The Magnitude and Drivers of Methane Ebullition and Diffusion Vary on a Longitudinal Gradient in a Small Freshwater Reservoir

Journal of geophysical research. Biogeosciences, 2020-03, Vol.125 (3), p.n/a

2020

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The family of bacterial ADP-ribosylating exotoxins

Clinical Microbiology Reviews, 1995-01, Vol.8 (1), p.34-47

1995

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Pharmacological classification of histamine H3 receptor agents across species is attributable to transmembrane 3 sequence differences

Inflammation research, 2007-04, Vol.56 Suppl 1 (S1), p.S45-S46

2007

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Clathrin-mediated Endocytosis of the β-Adrenergic Receptor Is Regulated by Phosphorylation/Dephosphorylation of β-Arrestin1

The Journal of biological chemistry, 1997-12, Vol.272 (49), p.31051-31057

1997

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Assignment of functional domains involved in ADP-ribosylation and B-oligomer binding within the carboxyl terminus of the S1 subunit of pertussis toxin

Infection and Immunity, 1994-05, Vol.62 (5), p.2071-2078

1994

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Structure-activity relationships of A-331440: a new histamine-3 antagonist with anti-obesity properties

Inflammation research, 2004-03, Vol.53 Suppl 1, p.S79-S80

2004

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Molecular characterization of the in vitro activation of pertussis toxin by ATP

The Journal of biological chemistry, 1993-06, Vol.268 (17), p.12570-12578

1993

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The carboxyl terminus of the S1 subunit of pertussis toxin confers high affinity binding to transducin

The Journal of biological chemistry, 1991-12, Vol.266 (35), p.23810-23814

1991

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Antiobesity evaluation of histamine H3 receptor (H3R) antagonist analogs of A-331440 with improved safety and efficacy

Inflammation research, 2005-04, Vol.54 Suppl 1 (S1), p.S27-S29

2005

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A new family of histamine H3 receptor antagonists based on a natural product: discovery, SAR, and properties of the series

Inflammation research, 2007-04, Vol.56 Suppl 1 (S1), p.S47-S48

2007

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Selective H3 receptor (H3R) blockade: broad efficacy in cognition and schizophrenia

Inflammation research, 2005-04, Vol.54 Suppl 1, p.S23-S24

2005

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Differences in pharmacological properties of histamine H3 receptor agonists and antagonists revealed at two human H3 receptor isoforms

Inflammation research, 2006-04, Vol.55 (S1), p.S45-S46

2006

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Protease treatment of pertussis toxin identifies the preferential cleavage of the S1 subunit

The Journal of biological chemistry, 1991-05, Vol.266 (13), p.8122-8128

1991

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Receptor-tyrosine-kinase- and Gβγ-mediated MAP kinase activation by a common signalling pathway

Nature (London), 1995-08, Vol.376 (6543), p.781-784

1995

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Use of novel, non-imidazole inverse agonist radioligands to define histamine H3 receptor pharmacology

Inflammation research, 2005-04, Vol.54 Suppl 1 (S1), p.S46-S47

2005

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Distinctions and contradistinctions between antiobesity histamine H3 receptor (H3R) antagonists compared to cognition-enhancing H3 receptor antagonists

Inflammation research, 2006-04, Vol.55 (S1), p.S42-S44

2006

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2. Histaminergic mechanisms in the CNS: Selective H3 receptor (H3R) blockade: broad efficacy in cognition and schizophrenia

Inflammation research, 2005-04, Vol.54 (S1), p.S23-S24

2005

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Effect of selegiline on speech performance in Parkinson's disease

Folia phoniatrica, 1993, Vol.45 (1), p.40-46

1993

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Characterization of Nanocrystalline CdSe by Size Exclusion Chromatography

Analytical chemistry (Washington), 2005-06, Vol.77 (11), p.3511-3515

2005

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Pharmacological Properties of ABT-239 [4-(2-{2-[(2 R )-2-Methylpyrrolidinyl]ethyl}-benzofuran-5-yl)benzonitrile]: II. Neurophysiological Characterization and Broad Preclinical Efficacy in Cognition and Schizophrenia of a Potent and Selective Histamine H 3 Receptor Antagonist

The Journal of pharmacology and experimental therapeutics, 2005-04, Vol.313 (1), p.176-190

2005

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D-alanine piperazine-amides: novel non-imidazole antagonists of the histamine H3 receptor

Inflammation research, 2003-04, Vol.52 Suppl 1, p.S47-S48

2003

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Recycling Size Exclusion Chromatography for the Analysis and Separation of Nanocrystalline Gold

Analytical chemistry (Washington), 2004-10, Vol.76 (19), p.5903-5910

2004

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In vitro pharmacological properties of two novel non-imidazole H3 receptor (H3R) antagonists

Inflammation research, 2003-04, Vol.52 Suppl 1, p.S45-S46

2003

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The use of heat transfer fluids in the synthesis of high-quality CdSe quantum dots, core/shell quantum dots, and quantum rods

Nanotechnology, 2005-10, Vol.16 (10), p.2000-2011

2005

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D-alanine piperazine-amides: novel non-imidazole antagonists of the histamine H 3 receptor

Inflammation research, 2003-04, Vol.52, p.s47-s48

2003

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The Magnitude and Drivers of Methane Ebullition and Diffusion Vary on a Longitudinal Gradient in a Small Freshwater Reservoir

The family of bacterial ADP-ribosylating exotoxins

Pharmacological classification of histamine H3 receptor agents across species is attributable to transmembrane 3 sequence differences

Clathrin-mediated Endocytosis of the β-Adrenergic Receptor Is Regulated by Phosphorylation/Dephosphorylation of β-Arrestin1

Assignment of functional domains involved in ADP-ribosylation and B-oligomer binding within the carboxyl terminus of the S1 subunit of pertussis toxin

Structure-activity relationships of A-331440: a new histamine-3 antagonist with anti-obesity properties

Molecular characterization of the in vitro activation of pertussis toxin by ATP

The carboxyl terminus of the S1 subunit of pertussis toxin confers high affinity binding to transducin

Antiobesity evaluation of histamine H3 receptor (H3R) antagonist analogs of A-331440 with improved safety and efficacy

A new family of histamine H3 receptor antagonists based on a natural product: discovery, SAR, and properties of the series

Selective H3 receptor (H3R) blockade: broad efficacy in cognition and schizophrenia

Differences in pharmacological properties of histamine H3 receptor agonists and antagonists revealed at two human H3 receptor isoforms

Protease treatment of pertussis toxin identifies the preferential cleavage of the S1 subunit

Receptor-tyrosine-kinase- and Gβγ-mediated MAP kinase activation by a common signalling pathway

Use of novel, non-imidazole inverse agonist radioligands to define histamine H3 receptor pharmacology

Distinctions and contradistinctions between antiobesity histamine H3 receptor (H3R) antagonists compared to cognition-enhancing H3 receptor antagonists

2. Histaminergic mechanisms in the CNS: Selective H3 receptor (H3R) blockade: broad efficacy in cognition and schizophrenia

Effect of selegiline on speech performance in Parkinson's disease

Characterization of Nanocrystalline CdSe by Size Exclusion Chromatography

Pharmacological Properties of ABT-239 [4-(2-{2-[(2 R )-2-Methylpyrrolidinyl]ethyl}-benzofuran-5-yl)benzonitrile]: II. Neurophysiological Characterization and Broad Preclinical Efficacy in Cognition and Schizophrenia of a Potent and Selective Histamine H 3 Receptor Antagonist

D-alanine piperazine-amides: novel non-imidazole antagonists of the histamine H3 receptor

Recycling Size Exclusion Chromatography for the Analysis and Separation of Nanocrystalline Gold

In vitro pharmacological properties of two novel non-imidazole H3 receptor (H3R) antagonists

The use of heat transfer fluids in the synthesis of high-quality CdSe quantum dots, core/shell quantum dots, and quantum rods

D-alanine piperazine-amides: novel non-imidazole antagonists of the histamine H 3 receptor

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