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Veterinary and Human Toxicology
|
February 1, 1991
Hazards in confinement housing--gases and dusts in confined animal houses for swine, poultry, horses and humans
J Pickrell
Science (New York, N.Y.)
|
February 24, 2001
U.K. science budget. Gene jocks, data crunchers hit jackpot
J Pickrell
Archives of Pathology & Laboratory Medicine
|
August 1, 1990
Three cases of fatal cardiac tamponade following ventricular endocardial biopsy
C M Craven, T Allred, S L Garry, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 30, 2008
Structure-guided design of substituted aza-benzimidazoles as potent hypoxia inducible factor-1alpha prolyl hydroxylase-2 inhibitors
Mike Frohn, Vellarkad Viswanadhan, Alexander J Pickrell, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 22, 2011
Novel 5- and 6-subtituted benzothiazoles with improved physicochemical properties: potent S1P₁ agonists with in vivo lymphocyte-depleting activity
Mike Frohn, Victor J Cee, Brian A Lanman, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 20, 2012
Isoform-selective thiazolo[5,4-b]pyridine S1P1 agonists possessing acyclic amino carboxylate head-groups
Anthony B Reed, Brian A Lanman, Susana Neira, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 15, 2013
The optimization of aminooxadiazoles as orally active inhibitors of Cdc7
Paul E Harrington, Matthew P Bourbeau, Christopher Fotsch, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
4-Methoxy-N-[2-(trifluoromethyl)biphenyl-4-ylcarbamoyl]nicotinamide: A Potent and Selective Agonist of S1P1
Lewis D Pennington, Kelvin K C Sham, Alexander J Pickrell, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Optimization of a Potent, Orally Active S1P1 Agonist Containing a Quinolinone Core
Paul E Harrington, Michael D Croghan, Christopher Fotsch, et al.
ACS Chemical Biology
|
July 20, 2016
Facile Modulation of Antibody Fucosylation with Small Molecule Fucostatin Inhibitors and Cocrystal Structure with GDP-Mannose 4,6-Dehydratase
John G Allen, Mirna Mujacic, Michael J Frohn, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Veterinary and Human Toxicology
|
February 1, 1991
Hazards in confinement housing--gases and dusts in confined animal houses for swine, poultry, horses and humans
J Pickrell
Science (New York, N.Y.)
|
February 24, 2001
U.K. science budget. Gene jocks, data crunchers hit jackpot
J Pickrell
Archives of Pathology & Laboratory Medicine
|
August 1, 1990
Three cases of fatal cardiac tamponade following ventricular endocardial biopsy
C M Craven, T Allred, S L Garry, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 30, 2008
Structure-guided design of substituted aza-benzimidazoles as potent hypoxia inducible factor-1alpha prolyl hydroxylase-2 inhibitors
Mike Frohn, Vellarkad Viswanadhan, Alexander J Pickrell, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 22, 2011
Novel 5- and 6-subtituted benzothiazoles with improved physicochemical properties: potent S1P₁ agonists with in vivo lymphocyte-depleting activity
Mike Frohn, Victor J Cee, Brian A Lanman, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 20, 2012
Isoform-selective thiazolo[5,4-b]pyridine S1P1 agonists possessing acyclic amino carboxylate head-groups
Anthony B Reed, Brian A Lanman, Susana Neira, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 15, 2013
The optimization of aminooxadiazoles as orally active inhibitors of Cdc7
Paul E Harrington, Matthew P Bourbeau, Christopher Fotsch, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
4-Methoxy-N-[2-(trifluoromethyl)biphenyl-4-ylcarbamoyl]nicotinamide: A Potent and Selective Agonist of S1P1
Lewis D Pennington, Kelvin K C Sham, Alexander J Pickrell, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Optimization of a Potent, Orally Active S1P1 Agonist Containing a Quinolinone Core
Paul E Harrington, Michael D Croghan, Christopher Fotsch, et al.
ACS Chemical Biology
|
July 20, 2016
Facile Modulation of Antibody Fucosylation with Small Molecule Fucostatin Inhibitors and Cocrystal Structure with GDP-Mannose 4,6-Dehydratase
John G Allen, Mirna Mujacic, Michael J Frohn, et al.
Page
of 2