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At the Intersection of Industry, Academia, and Government: How Do We Facilitate Productive Precision Livestock Farming in Practice?

Animals (Basel), 2019-08, Vol.9 (9), p.635

2019

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Discovery of N‑(6-Fluoro-1-oxo-1,2-dihydroisoquinolin-7-yl)-5-[(3R)‑3-hydroxypyrrolidin-1-yl]thiophene-2-sulfonamide (LSN 3213128), a Potent and Selective Nonclassical Antifolate Aminoimidazole-4-carboxamide Ribonucleotide Formyltransferase (AICARFT) Inhibitor Effective at Tumor Suppression in a Cancer Xenograft Model

Journal of medicinal chemistry, 2017-12, Vol.60 (23), p.9599-9616

2017

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Ammonia and greenhouse gas emissions from a modern U.S. swine breeding-gestation-farrowing system

Atmospheric environment (1994), 2014-12, Vol.98, p.620-628

2014

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Characterization of a novel AICARFT inhibitor which potently elevates ZMP and has anti-tumor activity in murine models

Scientific reports, 2018-10, Vol.8 (1), p.15458-12, Article 15458

2018

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Modelling ventilation rate, balance temperature and supplemental heat need in alternative vs. conventional laying-hen housing systems

Biosystems engineering, 2013-07, Vol.115 (3), p.311-323

2013

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Design and Synthesis of a Novel Series of 1,2-Disubstituted Cyclopentanes as Small, Potent Potentiators of 2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propanoic Acid (AMPA) Receptors

Journal of medicinal chemistry, 2002-05, Vol.45 (10), p.2101-2111

2002

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A Selective Estrogen Receptor Modulator Designed for the Treatment of Uterine Leiomyoma with Unique Tissue Specificity for Uterus and Ovaries in Rats

Journal of medicinal chemistry, 2005-11, Vol.48 (22), p.6772-6775

2005

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Silent Intralesional Microhemorrhage as a Risk Factor for Brain Arteriovenous Malformation Rupture

Stroke (1970), 2012-05, Vol.43 (5), p.1240-1246

2012

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A New Selective Estrogen Receptor Modulator with Potent Uterine Antagonist Activity, Agonist Activity in Bone, and Minimal Ovarian Stimulation

Endocrinology (Philadelphia), 2005-10, Vol.146 (10), p.4524-4535

2005

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Structure–activity relationships of SERMs optimized for uterine antagonism and ovarian safety

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (13), p.3544-3549

2007

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Design of Antitumor Prodrugs: Substrates for Antibody Targeted Enzymes

Chemical reviews, 1994-09, Vol.94 (6), p.1553-1566

1994

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Synthesis and Evaluation of Peptidyl Michael Acceptors That Inactivate Human Rhinovirus 3C Protease and Inhibit Virus Replication

Journal of medicinal chemistry, 1998-07, Vol.41 (14), p.2579-2587

1998

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Synthesis and biological activity of the putative metabolites of the atypical antipsychotic agent tiospirone

Journal of medicinal chemistry, 1991-11, Vol.34 (11), p.3316-3328

1991

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Progress toward the discovery and development of efficacious BACE inhibitors

Current opinion in drug discovery & development, 2006-11, Vol.9 (6), p.776

2006

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Potent Human Immunodeficiency Virus Type 1 Protease Inhibitors That Utilize Noncoded d-Amino Acids as P2/P3 Ligands

Journal of medicinal chemistry, 1996-01, Vol.39 (1), p.96-108

1996

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Development of analytical and preparative chromatographic separations of novel growth hormone secretagogue compounds

Journal of Chromatography A, 2000-03, Vol.872 (1), p.75-84

2000

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Symmetric positive 4th order tensors & their estimation from diffusion weighted MRI

Information processing in medical imaging : proceedings of the ... conference, 2007, Vol.20, p.308

2007

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Synthesis of acylhydrazido-substituted cephems. Design of cephalosporin-vinca alkaloid prodrugs: substrates for an antibody targeted enzyme

Journal of organic chemistry, 1992-04, Vol.57 (8), p.2334-2340

1992

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Site-Specific Prodrug Activation by Antibody-.beta.-Lactamase Conjugates: Preclinical Investigation of the Efficacy and Toxicity of Doxorubicin Delivered by Antibody Directed Catalysis

Bioconjugate chemistry, 1995-07, Vol.6 (4), p.440-446

1995

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Radical-cation-initiated Diels-Alder di- and trimerization of 3,4-dimethoxypropenylbenzene: stereochemical correlation with the lignans galbulin and isogalbulin

Journal of the American Chemical Society, 1989-03, Vol.111 (5), p.1749-1754

1989

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O1-06-02: The design and synthesis of an efficacious BACE inhibitor

Alzheimer's & dementia, 2006-07, Vol.2 (3), p.S20-S20

2006

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Small peptidic aldehyde inhibitors of human rhinovirus 3C protease

Bioorganic & medicinal chemistry letters, 1996-12, Vol.6 (23), p.2893-2896

1996

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Development ofin VitroPeptide Substrates for Human Rhinovirus-14 2A Protease

Archives of biochemistry and biophysics, 1998-08, Vol.356 (1), p.12-18

1998

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Site-specific prodrug activation by antibody-β-lactamase conjugates : regression and long-term growth inhibition of human colon carcinoma xenograft models

Cancer research (Chicago, Ill.), 1993-09, Vol.53 (17), p.3956-3963

1993

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Development of in vitro peptide substrates for human rhinovirus-14 2A protease

Archives of biochemistry and biophysics, 1998-08, Vol.356 (1), p.12-18

1998

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At the Intersection of Industry, Academia, and Government: How Do We Facilitate Productive Precision Livestock Farming in Practice?

Ammonia and greenhouse gas emissions from a modern U.S. swine breeding-gestation-farrowing system

Characterization of a novel AICARFT inhibitor which potently elevates ZMP and has anti-tumor activity in murine models

Modelling ventilation rate, balance temperature and supplemental heat need in alternative vs. conventional laying-hen housing systems

Design and Synthesis of a Novel Series of 1,2-Disubstituted Cyclopentanes as Small, Potent Potentiators of 2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propanoic Acid (AMPA) Receptors

A Selective Estrogen Receptor Modulator Designed for the Treatment of Uterine Leiomyoma with Unique Tissue Specificity for Uterus and Ovaries in Rats

Silent Intralesional Microhemorrhage as a Risk Factor for Brain Arteriovenous Malformation Rupture

A New Selective Estrogen Receptor Modulator with Potent Uterine Antagonist Activity, Agonist Activity in Bone, and Minimal Ovarian Stimulation

Structure–activity relationships of SERMs optimized for uterine antagonism and ovarian safety

Design of Antitumor Prodrugs: Substrates for Antibody Targeted Enzymes

Synthesis and Evaluation of Peptidyl Michael Acceptors That Inactivate Human Rhinovirus 3C Protease and Inhibit Virus Replication

Synthesis and biological activity of the putative metabolites of the atypical antipsychotic agent tiospirone

Progress toward the discovery and development of efficacious BACE inhibitors

Potent Human Immunodeficiency Virus Type 1 Protease Inhibitors That Utilize Noncoded d-Amino Acids as P2/P3 Ligands

Development of analytical and preparative chromatographic separations of novel growth hormone secretagogue compounds

Symmetric positive 4th order tensors & their estimation from diffusion weighted MRI

Synthesis of acylhydrazido-substituted cephems. Design of cephalosporin-vinca alkaloid prodrugs: substrates for an antibody targeted enzyme

Site-Specific Prodrug Activation by Antibody-.beta.-Lactamase Conjugates: Preclinical Investigation of the Efficacy and Toxicity of Doxorubicin Delivered by Antibody Directed Catalysis

Radical-cation-initiated Diels-Alder di- and trimerization of 3,4-dimethoxypropenylbenzene: stereochemical correlation with the lignans galbulin and isogalbulin

O1-06-02: The design and synthesis of an efficacious BACE inhibitor

Small peptidic aldehyde inhibitors of human rhinovirus 3C protease

Development ofin VitroPeptide Substrates for Human Rhinovirus-14 2A Protease

Site-specific prodrug activation by antibody-β-lactamase conjugates : regression and long-term growth inhibition of human colon carcinoma xenograft models

Development of in vitro peptide substrates for human rhinovirus-14 2A protease

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