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The Journal of Antibiotics
|
November 1, 1995
Protein tyrosine kinase and protein kinase C inhibition by fungal anthraquinones related to emodin
A Fredenhagen, H Mett, T Meyer, et al.
International Journal of Cancer
|
May 15, 1989
A derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and in vitro anti-proliferative as well as in vivo anti-tumor activity
T Meyer, U Regenass, D Fabbro, et al.
International Journal of Cancer
|
June 25, 1998
Reversal of multidrug resistance by the staurosporine derivatives CGP 41251 and CGP 42700
I Utz, M Spitaler, M Rybczynska, et al.
International Journal of Cancer
|
May 21, 1999
Author errata
T Meyer, U Regenass, D Fabbro, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1993
Pharmacological properties of the ornithine decarboxylase inhibitor 3-aminooxy-1-propanamine and several structural analogues
H Mett, J Stanek, J A Lopez-Ballester, 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.
Cancer Research
|
September 1, 1992
New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity
U Regenass, G Caravatti, H Mett, 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.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 1, 1995
4,5-bis(4-fluoroanilino)phthalimide: A selective inhibitor of the epidermal growth factor receptor signal transduction pathway with potent in vivo antitumor activity
E Buchdunger, H Mett, U Trinks, et al.
The Journal of Biological Chemistry
|
December 25, 1990
Thiazolidine-diones. Biochemical and biological activity of a novel class of tyrosine protein kinase inhibitors
J F Geissler, P Traxler, U Regenass, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
The Journal of Antibiotics
|
November 1, 1995
Protein tyrosine kinase and protein kinase C inhibition by fungal anthraquinones related to emodin
A Fredenhagen, H Mett, T Meyer, et al.
International Journal of Cancer
|
May 15, 1989
A derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and in vitro anti-proliferative as well as in vivo anti-tumor activity
T Meyer, U Regenass, D Fabbro, et al.
International Journal of Cancer
|
June 25, 1998
Reversal of multidrug resistance by the staurosporine derivatives CGP 41251 and CGP 42700
I Utz, M Spitaler, M Rybczynska, et al.
International Journal of Cancer
|
May 21, 1999
Author errata
T Meyer, U Regenass, D Fabbro, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1993
Pharmacological properties of the ornithine decarboxylase inhibitor 3-aminooxy-1-propanamine and several structural analogues
H Mett, J Stanek, J A Lopez-Ballester, 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.
Cancer Research
|
September 1, 1992
New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity
U Regenass, G Caravatti, H Mett, 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.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 1, 1995
4,5-bis(4-fluoroanilino)phthalimide: A selective inhibitor of the epidermal growth factor receptor signal transduction pathway with potent in vivo antitumor activity
E Buchdunger, H Mett, U Trinks, et al.
The Journal of Biological Chemistry
|
December 25, 1990
Thiazolidine-diones. Biochemical and biological activity of a novel class of tyrosine protein kinase inhibitors
J F Geissler, P Traxler, U Regenass, et al.
Page
of 4