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Activation of the G-Protein-Coupled Receptor 119: A Conformation-Based Hypothesis for Understanding Agonist Response

Journal of medicinal chemistry, 2011-03, Vol.54 (6), p.1948-1952

2011

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Application of Flow and Biocatalytic Transaminase Technology for the Synthesis of a 1‑Oxa-8-azaspiro[4.5]decan-3-amine

Organic process research & development, 2022-03, Vol.26 (3), p.616-623

2022

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Cell‐free in vitro reduction of carboxylates to aldehydes: With crude enzyme preparations to a key pharmaceutical building block

Biotechnology journal, 2021-04, Vol.16 (4), p.e2000315-n/a

2021

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ChemInform Abstract: Expedient Synthesis of Novel [beta]-Ketoesters from the Mizoroki--Heck Coupling of Ethyl 3-Ethoxyacrylate with Aryl and Pyridyl Halides

ChemInform, 2014-04, Vol.45 (14)

2014

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ChemInform Abstract: Expedient Synthesis of Novel β-Ketoesters from the Mizoroki-Heck Coupling of Ethyl 3-Ethoxyacrylate with Aryl and Pyridyl Halides

ChemInform, 2014-04, Vol.45 (14), p.no-no

2014

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ChemInform Abstract: Fluorodecarboxylation for the Synthesis of Trifluoromethyl Aryl Ethers

ChemInform, 2016-11, Vol.47 (50), p.no-no

2016

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CITN11-02 interim trial results: subcutaneous administration of recombinant human IL-15

Journal for immunotherapy of cancer, 2015-11, Vol.3 (Suppl 2)

2015

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CITN11-02 interim trial results: subcutaneous administration of recombinant human IL-15 (rhIL-15) is associated with expansion of peripheral blood CD56+ NK cells and CD8+ T cells

Journal for immunotherapy of cancer, 2015-11, Vol.3 (Suppl 2), p.P203-P203, Article P203

2015

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CITN11-02 interim trial results: subcutaneous administration of recombinant human IL-15 (rhil-15) is associated with robust expansion of peripheral blood CD56+ NK cells

Journal for immunotherapy of cancer, 2014-11, Vol.2 (S3), p.P80-P80, Article P80

2014

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CITN11-02 phase I trial of subcutaneous recombinant human IL-15 (rhIL-15) is associated with expansion of circulating CD56+ NK cells and CD8+ T cells

The Journal of immunology (1950), 2016-05, Vol.196 (1_Supplement), p.75-75.16

2016

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Cytotoxic T lymphocyte responses against melanocytes and melanoma

Journal of translational medicine, 2011-07, Vol.9 (1), p.122-122, Article 122

2011

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The Discovery of (2R,4R)-N-(4-chlorophenyl)-N- (2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)-4-methoxypyrrolid ine-1,2-dicarboxamide (PD 0348292), an Orally Efficacious Factor Xa Inhibitor

Chemical biology & drug design, 2007-08, Vol.70 (2), p.100-112

2007

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The Discovery of (2R,4R)-N-(4-chlorophenyl)-N- (2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)-4-methoxypyrrolidine-1,2-dicarboxamide (PD 0348292), an Orally Efficacious Factor Xa Inhibitor

Chemical biology & drug design, 2007-08, Vol.70 (2), p.100-112

2007

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The discovery of fluoropyridine-based inhibitors of the Factor VIIa/TF complex

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (21), p.4752-4756

2005

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The Discovery of Fluoropyridine-Based Inhibitors of the Factor VIIa/TF Complex

ChemInform, 2006-01, Vol.37 (4), p.no-no

2006

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The discovery of fluoropyridine-based inhibitors of the factor VIIa/TF complex—Part 2

Bioorganic & medicinal chemistry letters, 2006-02, Vol.16 (4), p.1060-1064

2006

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The Discovery of Fluoropyridine-Based Inhibitors of the Factor VIIa/TF Complex. Part 2

ChemInform, 2006-05, Vol.37 (21), p.no-no

2006

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The discovery of glycine and related amino acid-based factor Xa inhibitors

Bioorganic & medicinal chemistry, 2006-07, Vol.14 (13), p.4379-4392

2006

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Discovery of new piperidine amide triazolobenzodiazepinones as intestinal-selective CCK1 receptor agonists

Bioorganic & medicinal chemistry letters, 2012-04, Vol.22 (8), p.2943-2947

2012

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An efficient synthesis of 2-(3-(4-amidinophenylcarbamoyl)naphthalen-2-yl)-5-((2,2-methylpropyl)carbamoyl)benzoic acid: a factor VIIa inhibitor discovered by the Ono Pharmaceutical Company

Tetrahedron letters, 2000, Vol.41 (32), p.6041-6044

2000

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Enantioselective Single and Dual α‑C–H Bond Functionalization of Cyclic Amines via Enzymatic Carbene Transfer

Journal of the American Chemical Society, 2023-01, Vol.145 (1), p.537-550

2023

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Ethnographic Methods for Identifying Cultural Concepts of Distress: Developing Reliable and Valid Measures

Field Methods, 2023-08, Vol.35 (3), p.175-197

2023

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Expedient synthesis of novel β-ketoesters from the Mizoroki–Heck coupling of ethyl 3-ethoxyacrylate with aryl and pyridyl halides

Tetrahedron letters, 2013-12, Vol.54 (51), p.7065-7068

2013

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Exploration of 4,4-disubstituted pyrrolidine-1,2-dicarboxamides as potent, orally active Factor Xa inhibitors with extended duration of action

Bioorganic & medicinal chemistry, 2009-03, Vol.17 (6), p.2501-2511

2009

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Festive Fighting and Forgiving: Ritual and Resilience among Indigenous Indian "Conservation Refugees"

Global Mental Health, 2015, p.173-190

1, 2015

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Activation of the G-Protein-Coupled Receptor 119: A Conformation-Based Hypothesis for Understanding Agonist Response

Application of Flow and Biocatalytic Transaminase Technology for the Synthesis of a 1‑Oxa-8-azaspiro[4.5]decan-3-amine

Cell‐free in vitro reduction of carboxylates to aldehydes: With crude enzyme preparations to a key pharmaceutical building block

ChemInform Abstract: Expedient Synthesis of Novel [beta]-Ketoesters from the Mizoroki--Heck Coupling of Ethyl 3-Ethoxyacrylate with Aryl and Pyridyl Halides

ChemInform Abstract: Expedient Synthesis of Novel β-Ketoesters from the Mizoroki-Heck Coupling of Ethyl 3-Ethoxyacrylate with Aryl and Pyridyl Halides

ChemInform Abstract: Fluorodecarboxylation for the Synthesis of Trifluoromethyl Aryl Ethers

CITN11-02 interim trial results: subcutaneous administration of recombinant human IL-15

CITN11-02 interim trial results: subcutaneous administration of recombinant human IL-15 (rhIL-15) is associated with expansion of peripheral blood CD56+ NK cells and CD8+ T cells

CITN11-02 interim trial results: subcutaneous administration of recombinant human IL-15 (rhil-15) is associated with robust expansion of peripheral blood CD56+ NK cells

CITN11-02 phase I trial of subcutaneous recombinant human IL-15 (rhIL-15) is associated with expansion of circulating CD56+ NK cells and CD8+ T cells

Cytotoxic T lymphocyte responses against melanocytes and melanoma

The Discovery of (2R,4R)-N-(4-chlorophenyl)-N- (2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)-4-methoxypyrrolid ine-1,2-dicarboxamide (PD 0348292), an Orally Efficacious Factor Xa Inhibitor

The Discovery of (2R,4R)-N-(4-chlorophenyl)-N- (2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)-4-methoxypyrrolidine-1,2-dicarboxamide (PD 0348292), an Orally Efficacious Factor Xa Inhibitor

The discovery of fluoropyridine-based inhibitors of the Factor VIIa/TF complex

The Discovery of Fluoropyridine-Based Inhibitors of the Factor VIIa/TF Complex

The discovery of fluoropyridine-based inhibitors of the factor VIIa/TF complex—Part 2

The Discovery of Fluoropyridine-Based Inhibitors of the Factor VIIa/TF Complex. Part 2

The discovery of glycine and related amino acid-based factor Xa inhibitors

Discovery of new piperidine amide triazolobenzodiazepinones as intestinal-selective CCK1 receptor agonists

An efficient synthesis of 2-(3-(4-amidinophenylcarbamoyl)naphthalen-2-yl)-5-((2,2-methylpropyl)carbamoyl)benzoic acid: a factor VIIa inhibitor discovered by the Ono Pharmaceutical Company

Enantioselective Single and Dual α‑C–H Bond Functionalization of Cyclic Amines via Enzymatic Carbene Transfer

Ethnographic Methods for Identifying Cultural Concepts of Distress: Developing Reliable and Valid Measures

Expedient synthesis of novel β-ketoesters from the Mizoroki–Heck coupling of ethyl 3-ethoxyacrylate with aryl and pyridyl halides

Exploration of 4,4-disubstituted pyrrolidine-1,2-dicarboxamides as potent, orally active Factor Xa inhibitors with extended duration of action

Festive Fighting and Forgiving: Ritual and Resilience among Indigenous Indian "Conservation Refugees"

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