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Agreement between fragility fracture risk assessment algorithms as applied to adults with chronic spinal cord injury

Spinal cord, 2017-11, Vol.55 (11), p.985-993

2017

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Applications of Vinylogous Mannich Reactions. Total Syntheses of the Ergot Alkaloids Rugulovasines A and B and Setoclavine

Journal of the American Chemical Society, 2001-06, Vol.123 (25), p.5918-5924

2001

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Developmental Range of Reflective Judgment: The Effect of Contextual Support and Practice on Developmental Stage

Developmental psychology, 1993-09, Vol.29 (5), p.893-906

1993

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Alteration of Lymphocyte Trafficking by Sphingosine-1-Phosphate Receptor Agonists

Science (American Association for the Advancement of Science), 2002-04, Vol.296 (5566), p.346-349

2002

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Potent 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists: effects of fused heterocycles on antiviral activity and pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 2005-04, Vol.15 (8), p.2129-2134

2005

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A Rational Utilization of High-Throughput Screening Affords Selective, Orally Bioavailable 1-Benzyl-3-carboxyazetidine Sphingosine-1-phosphate-1 Receptor Agonists

Journal of medicinal chemistry, 2004-12, Vol.47 (27), p.6662-6665

2004

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Binding of 2-Aryl-4-(piperidin-1-yl)butanamines and 1,3,4-Trisubstituted Pyrrolidines to Human CCR5: A Molecular Modeling-Guided Mutagenesis Study of the Binding Pocket

Biochemistry (Easton), 2003-02, Vol.42 (6), p.1544-1550

2003

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Comparison of ambulatory and inpatient experiences in five specialties

Medical teacher, 1999, Vol.21 (6), p.594-596

C Lynch Theodore W Whitley L Lorraine Basnight Timothy Patselas, D

1999

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Constructing Networks of Action-Relevant Episodes: An In Situ Research Methodology

The Journal of the learning sciences, 2001-01, Vol.10 (1-2), p.63-112

2001

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Multiple congenital defects following maternal varicella; report of a case

The New England journal of medicine, 1947-04, Vol.236 (15), p.534

1947

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How a technology professional development program fits into teachers’ work life

Teaching and teacher education, 2003-08, Vol.19 (6), p.591-607

Yamagata-Lynch, Lisa C

2003

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2-Aryl(pyrrolidin-4-yl)acetic acids are potent agonists of sphingosine-1-phosphate (S1P) receptors

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (13), p.3564-3568

2006

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1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists: modifications of the arylpropylpiperidine side chains

Bioorganic & medicinal chemistry letters, 2003-01, Vol.13 (1), p.119-123

2003

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Design and synthesis of conformationally constrained 3-( N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors

Bioorganic & medicinal chemistry letters, 2004-10, Vol.14 (19), p.4861-4866

2004

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Antagonists of human CCR5 receptor containing 4-(pyrazolyl)piperidine side chains. Part 2: Discovery of potent, selective, and orally bioavailable compounds

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (4), p.941-945

2004

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1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 4: Synthesis of N-1 acidic functionality affording analogues with enhanced antiviral activity against HIV

Bioorganic & medicinal chemistry letters, 2002-10, Vol.12 (20), p.3001-3004

2002

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Co-contraction of antagonist muscles during knee extension against gravity: Insights for functional electrical stimulation control design

2012 Annual International Conference of the IEEE Engineering in Medicine and Biology Society, 2012, Vol.2012, p.1843-1846

2012

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Supportive Classroom Environments For Creativity in Higher Education

The Journal of creative behavior, 1999-12, Vol.33 (4), p.277-293

1999

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CCR5 antagonists: bicyclic isoxazolidines as conformationally constrained N-1-substituted pyrrolidines

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (4), p.677-679

2002

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CCR5 Antagonists: 3-(Pyrrolidin-1-yl)propionic Acid Analogues with Potent Anti-HIV Activity

Organic letters, 2003-07, Vol.5 (14), p.2473-2475

2003

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GaAs Optical Parametric Oscillator with a Circularly Polarized Pump

2007 Conference on Lasers and Electro-Optics (CLEO), 2007, p.1-2

2007

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Discovery of Potent 3,5-Diphenyl-1,2,4-oxadiazole Sphingosine-1-phosphate-1 (S1P sub(1)) Receptor Agonists with Exceptional Selectivity against S1P sub(2) and S1P sub(3)

Journal of medicinal chemistry, 2005-10, Vol.48 (20), p.6169-6173

2005

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Consommations alimentaires de patients atteints par le syndrome de Lynch

Nutrition clinique et métabolisme, 2022-02, Vol.36 (1), p.S71-S71

2022

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Professional nursing issues in the administration of investigational antiarrhythmic medications

Heart & lung, 1984-07, Vol.13 (4), p.395-399

1984

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Application of AlMe3-mediated amidation reactions to solution phase peptide synthesis

Tetrahedron letters, 1998-03, Vol.39 (12), p.1517-1520

1998

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Agreement between fragility fracture risk assessment algorithms as applied to adults with chronic spinal cord injury

Applications of Vinylogous Mannich Reactions. Total Syntheses of the Ergot Alkaloids Rugulovasines A and B and Setoclavine

Developmental Range of Reflective Judgment: The Effect of Contextual Support and Practice on Developmental Stage

Alteration of Lymphocyte Trafficking by Sphingosine-1-Phosphate Receptor Agonists

Potent 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists: effects of fused heterocycles on antiviral activity and pharmacokinetic properties

A Rational Utilization of High-Throughput Screening Affords Selective, Orally Bioavailable 1-Benzyl-3-carboxyazetidine Sphingosine-1-phosphate-1 Receptor Agonists

Binding of 2-Aryl-4-(piperidin-1-yl)butanamines and 1,3,4-Trisubstituted Pyrrolidines to Human CCR5: A Molecular Modeling-Guided Mutagenesis Study of the Binding Pocket

Comparison of ambulatory and inpatient experiences in five specialties

Constructing Networks of Action-Relevant Episodes: An In Situ Research Methodology

Multiple congenital defects following maternal varicella; report of a case

How a technology professional development program fits into teachers’ work life

2-Aryl(pyrrolidin-4-yl)acetic acids are potent agonists of sphingosine-1-phosphate (S1P) receptors

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists: modifications of the arylpropylpiperidine side chains

Design and synthesis of conformationally constrained 3-( N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors

Antagonists of human CCR5 receptor containing 4-(pyrazolyl)piperidine side chains. Part 2: Discovery of potent, selective, and orally bioavailable compounds

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 4: Synthesis of N-1 acidic functionality affording analogues with enhanced antiviral activity against HIV

Co-contraction of antagonist muscles during knee extension against gravity: Insights for functional electrical stimulation control design

Supportive Classroom Environments For Creativity in Higher Education

CCR5 antagonists: bicyclic isoxazolidines as conformationally constrained N-1-substituted pyrrolidines

CCR5 Antagonists: 3-(Pyrrolidin-1-yl)propionic Acid Analogues with Potent Anti-HIV Activity

GaAs Optical Parametric Oscillator with a Circularly Polarized Pump

Discovery of Potent 3,5-Diphenyl-1,2,4-oxadiazole Sphingosine-1-phosphate-1 (S1P sub(1)) Receptor Agonists with Exceptional Selectivity against S1P sub(2) and S1P sub(3)

Consommations alimentaires de patients atteints par le syndrome de Lynch

Professional nursing issues in the administration of investigational antiarrhythmic medications

Application of AlMe3-mediated amidation reactions to solution phase peptide synthesis

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