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Blood
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November 14, 1997
The tyrosine kinase inhibitor CGP57148B selectively inhibits the growth of BCR-ABL-positive cells
M W Deininger, J M Goldman, N Lydon, et al.
Journal De Pharmacie De Belgique
|
March 1, 1997
Design and synthesis of novel tyrosine kinase inhibitors using a pharmacophore model of the ATP-binding site of the EGF-R
P Traxler, P Furet, H Mett, et al.
Journal of Medicinal Chemistry
|
June 7, 1996
4-(Phenylamino)pyrrolopyrimidines: potent and selective, ATP site directed inhibitors of the EGF-receptor protein tyrosine kinase
P M Traxler, P Furet, H Mett, et al.
Biochemical and Biophysical Research Communications
|
February 28, 1992
The angiotensin AT2 receptor stimulates protein tyrosine phosphatase activity and mediates inhibition of particulate guanylate cyclase
S P Bottari, I N King, S Reichlin, et al.
Journal of Computer-Aided Molecular Design
|
December 1, 1995
Modelling study of protein kinase inhibitors: binding mode of staurosporine and origin of the selectivity of CGP 52411
P Furet, G Caravatti, N Lydon, et al.
Experimental Cell Research
|
October 1, 1988
Electroporation of cultured adult rat hepatocytes with the c-myc gene potentiates DNA synthesis in response to epidermal growth factor
S F Muakkassah-Kelly, D A Jans, N Lydon, et al.
Journal of Medicinal Chemistry
|
June 23, 1995
[(Alkylamino)methyl]acrylophenones: potent and selective inhibitors of the epidermal growth factor receptor protein tyrosine kinase
P Traxler, U Trinks, E Buchdunger, et al.
International Journal of Cancer
|
May 21, 1999
Author errata
N Lydon, H Mett, M Mueller, et al.
Journal of Medicinal Chemistry
|
April 1, 1994
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinase
U Trinks, E Buchdunger, P Furet, et al.
Journal of Medicinal Chemistry
|
November 14, 1997
Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidines
P Traxler, G Bold, J Frei, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Blood
|
November 14, 1997
The tyrosine kinase inhibitor CGP57148B selectively inhibits the growth of BCR-ABL-positive cells
M W Deininger, J M Goldman, N Lydon, et al.
Journal De Pharmacie De Belgique
|
March 1, 1997
Design and synthesis of novel tyrosine kinase inhibitors using a pharmacophore model of the ATP-binding site of the EGF-R
P Traxler, P Furet, H Mett, et al.
Journal of Medicinal Chemistry
|
June 7, 1996
4-(Phenylamino)pyrrolopyrimidines: potent and selective, ATP site directed inhibitors of the EGF-receptor protein tyrosine kinase
P M Traxler, P Furet, H Mett, et al.
Biochemical and Biophysical Research Communications
|
February 28, 1992
The angiotensin AT2 receptor stimulates protein tyrosine phosphatase activity and mediates inhibition of particulate guanylate cyclase
S P Bottari, I N King, S Reichlin, et al.
Journal of Computer-Aided Molecular Design
|
December 1, 1995
Modelling study of protein kinase inhibitors: binding mode of staurosporine and origin of the selectivity of CGP 52411
P Furet, G Caravatti, N Lydon, et al.
Experimental Cell Research
|
October 1, 1988
Electroporation of cultured adult rat hepatocytes with the c-myc gene potentiates DNA synthesis in response to epidermal growth factor
S F Muakkassah-Kelly, D A Jans, N Lydon, et al.
Journal of Medicinal Chemistry
|
June 23, 1995
[(Alkylamino)methyl]acrylophenones: potent and selective inhibitors of the epidermal growth factor receptor protein tyrosine kinase
P Traxler, U Trinks, E Buchdunger, et al.
International Journal of Cancer
|
May 21, 1999
Author errata
N Lydon, H Mett, M Mueller, et al.
Journal of Medicinal Chemistry
|
April 1, 1994
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinase
U Trinks, E Buchdunger, P Furet, et al.
Journal of Medicinal Chemistry
|
November 14, 1997
Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidines
P Traxler, G Bold, J Frei, et al.
Page
of 2