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Clinical Endocrinology
|
December 1, 1979
An 'artificial beta cell' for control of diabetes mellitus: effect on plasma glucagon levels
D L Horwitz, B Gonen, J B Jaspan, et al.
Chest
|
July 23, 1998
Cutaneous zygomycosis (mucormycosis) complicating endotracheal intubation: diagnosis and successful treatment
M Dickinson, T Kalayanamit, C A Yang, et al.
The Pharmacogenomics Journal
|
December 14, 2011
A pharmacogenetic study of ADRB2 polymorphisms and indacaterol response in COPD patients
R Yelensky, Y Li, S Lewitzky, et al.
Archives of Neurology
|
September 12, 2007
Spinchter symptoms as predictors of long-term disability in multiple sclerosis
Margaret L Frazer, J Thomas Benson, Clare A Braun Hashemi, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 6, 2003
2,4-disubstituted pyrimidines: a novel class of KDR kinase inhibitors
Peter J Manley, Adrienne E Balitza, Mark T Bilodeau, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 6, 2004
The discovery of N-(1,3-thiazol-2-yl)pyridin-2-amines as potent inhibitors of KDR kinase
Mark T Bilodeau, Leonard D Rodman, Georgia B McGaughey, et al.
Pediatric Pulmonology
|
July 31, 2001
Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center study
P G Noone, N Hamblett, F Accurso, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 22, 2005
Potent 2-[(pyrimidin-4-yl)amine}-1,3-thiazole-5-carbonitrile-based inhibitors of VEGFR-2 (KDR) kinase
John T Sisko, Thomas J Tucker, Mark T Bilodeau, et al.
Diabetes Research and Clinical Practice
|
September 28, 1999
Diagnosis, screening and management of cystic fibrosis related diabetes mellitus: a consensus conference report
A Moran, D Hardin, D Rodman, et al.
Journal of Medicinal Chemistry
|
November 30, 2004
Potent N-(1,3-thiazol-2-yl)pyridin-2-amine vascular endothelial growth factor receptor tyrosine kinase inhibitors with excellent pharmacokinetics and low affinity for the hERG ion channel
Mark T Bilodeau, Adrienne E Balitza, Timothy J Koester, et al.
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of 2
Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Clinical Endocrinology
|
December 1, 1979
An 'artificial beta cell' for control of diabetes mellitus: effect on plasma glucagon levels
D L Horwitz, B Gonen, J B Jaspan, et al.
Chest
|
July 23, 1998
Cutaneous zygomycosis (mucormycosis) complicating endotracheal intubation: diagnosis and successful treatment
M Dickinson, T Kalayanamit, C A Yang, et al.
The Pharmacogenomics Journal
|
December 14, 2011
A pharmacogenetic study of ADRB2 polymorphisms and indacaterol response in COPD patients
R Yelensky, Y Li, S Lewitzky, et al.
Archives of Neurology
|
September 12, 2007
Spinchter symptoms as predictors of long-term disability in multiple sclerosis
Margaret L Frazer, J Thomas Benson, Clare A Braun Hashemi, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 6, 2003
2,4-disubstituted pyrimidines: a novel class of KDR kinase inhibitors
Peter J Manley, Adrienne E Balitza, Mark T Bilodeau, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 6, 2004
The discovery of N-(1,3-thiazol-2-yl)pyridin-2-amines as potent inhibitors of KDR kinase
Mark T Bilodeau, Leonard D Rodman, Georgia B McGaughey, et al.
Pediatric Pulmonology
|
July 31, 2001
Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center study
P G Noone, N Hamblett, F Accurso, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 22, 2005
Potent 2-[(pyrimidin-4-yl)amine}-1,3-thiazole-5-carbonitrile-based inhibitors of VEGFR-2 (KDR) kinase
John T Sisko, Thomas J Tucker, Mark T Bilodeau, et al.
Diabetes Research and Clinical Practice
|
September 28, 1999
Diagnosis, screening and management of cystic fibrosis related diabetes mellitus: a consensus conference report
A Moran, D Hardin, D Rodman, et al.
Journal of Medicinal Chemistry
|
November 30, 2004
Potent N-(1,3-thiazol-2-yl)pyridin-2-amine vascular endothelial growth factor receptor tyrosine kinase inhibitors with excellent pharmacokinetics and low affinity for the hERG ion channel
Mark T Bilodeau, Adrienne E Balitza, Timothy J Koester, et al.
Page
of 2