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Archives of Dermatological Research
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August 1, 1997
SCH 47112, a novel staurosporine derivative, inhibits 12-O-tetradecanoylphorbol-13-acetate-induced inflammation and epidermal hyperplasia in hairless mouse skin
N J Reynolds, S W McCombie, B B Shankar, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
June 17, 1999
Activity of SCH 66336, a tricyclic farnesyltransferase inhibitor, against human tumor colony-forming units
T Petit, E Izbicka, R A Lawrence, et al.
Cancer Chemotherapy and Pharmacology
|
December 29, 2000
The farnesyl protein transferase inhibitor SCH66336 synergizes with taxanes in vitro and enhances their antitumor activity in vivo
B Shi, B Yaremko, G Hajian, et al.
The Journal of Biological Chemistry
|
July 5, 1986
Quantitative measurement of sn-1,2-diacylglycerols present in platelets, hepatocytes, and ras- and sis-transformed normal rat kidney cells
J Preiss, C R Loomis, W R Bishop, et al.
Science (New York, N.Y.)
|
December 20, 1991
Identification and characterization of zinc binding sites in protein kinase C
S R Hubbard, W R Bishop, P Kirschmeier, et al.
The Journal of Biological Chemistry
|
May 15, 1992
Differential regulation of phosphoinositide and phosphatidylcholine hydrolysis by protein kinase C-beta 1 overexpression. Effects on stimulation by alpha-thrombin, guanosine 5'-O-(thiotriphosphate), and calcium
J A Pachter, J K Pai, R Mayer-Ezell, et al.
Bioorganic & Medicinal Chemistry
|
July 29, 1998
Synthesis of isomeric 3-piperidinyl and 3-pyrrolidinyl benzo[5,6]cyclohepta[1,2-b]pyridines: sulfonamido derivatives as inhibitors of Ras prenylation
J Kelly, R Wolin, M Connolly, et al.
The Journal of Biological Chemistry
|
June 15, 2000
Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules
H R Ashar, L James, K Gray, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Inhibitors of farnesyl protein transferase. Synthesis and biological activity of amide and cyanoguanidine derivatives containing a 5,11-dihydro[1]benzthiepin, benzoxepin, and benzazepin [4,3-b]pyridine ring system
R Wolin, M Connolly, J Kelly, et al.
The Journal of Biological Chemistry
|
December 22, 1995
Novel tricyclic inhibitors of farnesyl protein transferase. Biochemical characterization and inhibition of Ras modification in transfected Cos cells
W R Bishop, R Bond, J Petrin, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 6
Archives of Dermatological Research
|
August 1, 1997
SCH 47112, a novel staurosporine derivative, inhibits 12-O-tetradecanoylphorbol-13-acetate-induced inflammation and epidermal hyperplasia in hairless mouse skin
N J Reynolds, S W McCombie, B B Shankar, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
June 17, 1999
Activity of SCH 66336, a tricyclic farnesyltransferase inhibitor, against human tumor colony-forming units
T Petit, E Izbicka, R A Lawrence, et al.
Cancer Chemotherapy and Pharmacology
|
December 29, 2000
The farnesyl protein transferase inhibitor SCH66336 synergizes with taxanes in vitro and enhances their antitumor activity in vivo
B Shi, B Yaremko, G Hajian, et al.
The Journal of Biological Chemistry
|
July 5, 1986
Quantitative measurement of sn-1,2-diacylglycerols present in platelets, hepatocytes, and ras- and sis-transformed normal rat kidney cells
J Preiss, C R Loomis, W R Bishop, et al.
Science (New York, N.Y.)
|
December 20, 1991
Identification and characterization of zinc binding sites in protein kinase C
S R Hubbard, W R Bishop, P Kirschmeier, et al.
The Journal of Biological Chemistry
|
May 15, 1992
Differential regulation of phosphoinositide and phosphatidylcholine hydrolysis by protein kinase C-beta 1 overexpression. Effects on stimulation by alpha-thrombin, guanosine 5'-O-(thiotriphosphate), and calcium
J A Pachter, J K Pai, R Mayer-Ezell, et al.
Bioorganic & Medicinal Chemistry
|
July 29, 1998
Synthesis of isomeric 3-piperidinyl and 3-pyrrolidinyl benzo[5,6]cyclohepta[1,2-b]pyridines: sulfonamido derivatives as inhibitors of Ras prenylation
J Kelly, R Wolin, M Connolly, et al.
The Journal of Biological Chemistry
|
June 15, 2000
Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules
H R Ashar, L James, K Gray, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
Inhibitors of farnesyl protein transferase. Synthesis and biological activity of amide and cyanoguanidine derivatives containing a 5,11-dihydro[1]benzthiepin, benzoxepin, and benzazepin [4,3-b]pyridine ring system
R Wolin, M Connolly, J Kelly, et al.
The Journal of Biological Chemistry
|
December 22, 1995
Novel tricyclic inhibitors of farnesyl protein transferase. Biochemical characterization and inhibition of Ras modification in transfected Cos cells
W R Bishop, R Bond, J Petrin, et al.
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of 6