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Rhinology. Supplement
|
July 24, 2010
4-Phase-Rhinomanometry (4PR)--basics and practice 2010
Klaus Vogt, Alfredo A Jalowayski, W Althaus, et al.
Biochemical Pharmacology
|
March 22, 1996
The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase
I W Althaus, K C Chou, R J Lemay, et al.
Cancer Research
|
December 20, 2007
PF00299804, an irreversible pan-ERBB inhibitor, is effective in lung cancer models with EGFR and ERBB2 mutations that are resistant to gefitinib
Jeffrey A Engelman, Kreshnik Zejnullahu, Christopher-Michael Gale, et al.
Journal of Medicinal Chemistry
|
February 17, 2006
Tyrosine kinase inhibitors. 19. 6-Alkynamides of 4-anilinoquinazolines and 4-anilinopyrido[3,4-d]pyrimidines as irreversible inhibitors of the erbB family of tyrosine kinase receptors
Sylvester R Klutchko, Hairong Zhou, R Thomas Winters, et al.
Journal of Medicinal Chemistry
|
August 5, 2016
Tyrosine Kinase Inhibitors. 20. Optimization of Substituted Quinazoline and Pyrido[3,4-d]pyrimidine Derivatives as Orally Active, Irreversible Inhibitors of the Epidermal Growth Factor Receptor Family
Jeff B Smaill, Andrea J Gonzales, Julie A Spicer, et al.
Molecular Cancer Therapeutics
|
July 9, 2008
Antitumor activity and pharmacokinetic properties of PF-00299804, a second-generation irreversible pan-erbB receptor tyrosine kinase inhibitor
Andrea J Gonzales, Kenneth E Hook, Irene W Althaus, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 36) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 36 results.
Rhinology. Supplement
|
July 24, 2010
4-Phase-Rhinomanometry (4PR)--basics and practice 2010
Klaus Vogt, Alfredo A Jalowayski, W Althaus, et al.
Biochemical Pharmacology
|
March 22, 1996
The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase
I W Althaus, K C Chou, R J Lemay, et al.
Cancer Research
|
December 20, 2007
PF00299804, an irreversible pan-ERBB inhibitor, is effective in lung cancer models with EGFR and ERBB2 mutations that are resistant to gefitinib
Jeffrey A Engelman, Kreshnik Zejnullahu, Christopher-Michael Gale, et al.
Journal of Medicinal Chemistry
|
February 17, 2006
Tyrosine kinase inhibitors. 19. 6-Alkynamides of 4-anilinoquinazolines and 4-anilinopyrido[3,4-d]pyrimidines as irreversible inhibitors of the erbB family of tyrosine kinase receptors
Sylvester R Klutchko, Hairong Zhou, R Thomas Winters, et al.
Journal of Medicinal Chemistry
|
August 5, 2016
Tyrosine Kinase Inhibitors. 20. Optimization of Substituted Quinazoline and Pyrido[3,4-d]pyrimidine Derivatives as Orally Active, Irreversible Inhibitors of the Epidermal Growth Factor Receptor Family
Jeff B Smaill, Andrea J Gonzales, Julie A Spicer, et al.
Molecular Cancer Therapeutics
|
July 9, 2008
Antitumor activity and pharmacokinetic properties of PF-00299804, a second-generation irreversible pan-erbB receptor tyrosine kinase inhibitor
Andrea J Gonzales, Kenneth E Hook, Irene W Althaus, et al.
Page
of 4