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Endocrinology
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December 7, 2000
A role for Akt in mediating the estrogenic functions of epidermal growth factor and insulin-like growth factor I
M B Martin, T F Franke, G E Stoica, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 18, 2005
Phthalazinones 2: Optimisation and synthesis of novel potent inhibitors of poly(ADP-ribose)polymerase
Xiao-Ling Cockcroft, Krystyna J Dillon, Lesley Dixon, et al.
The Journal of Biological Chemistry
|
June 17, 1994
Effect of cadmium on estrogen receptor levels and estrogen-induced responses in human breast cancer cells
P Garcia-Morales, M Saceda, N Kenney, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 5, 2013
Optimization of potent and selective dual mTORC1 and mTORC2 inhibitors: the discovery of AZD8055 and AZD2014
Kurt G Pike, Karine Malagu, Marc G Hummersone, et al.
Organic & Biomolecular Chemistry
|
December 4, 2010
Synthesis of 4-alkyl-, 4-aryl- and 4-arylamino-5-aminoisoquinolin-1-ones and identification of a new PARP-2 selective inhibitor
Peter T Sunderland, Archana Dhami, Mary F Mahon, et al.
Journal of Medicinal Chemistry
|
October 1, 1988
Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesis
J B Summers, B P Gunn, J G Martin, et al.
British Journal of Cancer
|
October 27, 2005
Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026
B P Nutley, N F Smith, A Hayes, et al.
Cancer Research
|
December 18, 2004
Identification and characterization of a novel and specific inhibitor of the ataxia-telangiectasia mutated kinase ATM
Ian Hickson, Yan Zhao, Caroline J Richardson, et al.
American Journal of Hematology
|
January 1, 1993
Hepatic iron stores and plasma ferritin concentration in patients with sickle cell anemia and thalassemia major
G M Brittenham, A R Cohen, C E McLaren, et al.
Leukemia
|
June 2, 2007
TG101209, a small molecule JAK2-selective kinase inhibitor potently inhibits myeloproliferative disorder-associated JAK2V617F and MPLW515L/K mutations
A Pardanani, J Hood, T Lasho, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 98) with videos related to
Sort By:
Page
of 10
Endocrinology
|
December 7, 2000
A role for Akt in mediating the estrogenic functions of epidermal growth factor and insulin-like growth factor I
M B Martin, T F Franke, G E Stoica, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 18, 2005
Phthalazinones 2: Optimisation and synthesis of novel potent inhibitors of poly(ADP-ribose)polymerase
Xiao-Ling Cockcroft, Krystyna J Dillon, Lesley Dixon, et al.
The Journal of Biological Chemistry
|
June 17, 1994
Effect of cadmium on estrogen receptor levels and estrogen-induced responses in human breast cancer cells
P Garcia-Morales, M Saceda, N Kenney, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 5, 2013
Optimization of potent and selective dual mTORC1 and mTORC2 inhibitors: the discovery of AZD8055 and AZD2014
Kurt G Pike, Karine Malagu, Marc G Hummersone, et al.
Organic & Biomolecular Chemistry
|
December 4, 2010
Synthesis of 4-alkyl-, 4-aryl- and 4-arylamino-5-aminoisoquinolin-1-ones and identification of a new PARP-2 selective inhibitor
Peter T Sunderland, Archana Dhami, Mary F Mahon, et al.
Journal of Medicinal Chemistry
|
October 1, 1988
Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesis
J B Summers, B P Gunn, J G Martin, et al.
British Journal of Cancer
|
October 27, 2005
Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026
B P Nutley, N F Smith, A Hayes, et al.
Cancer Research
|
December 18, 2004
Identification and characterization of a novel and specific inhibitor of the ataxia-telangiectasia mutated kinase ATM
Ian Hickson, Yan Zhao, Caroline J Richardson, et al.
American Journal of Hematology
|
January 1, 1993
Hepatic iron stores and plasma ferritin concentration in patients with sickle cell anemia and thalassemia major
G M Brittenham, A R Cohen, C E McLaren, et al.
Leukemia
|
June 2, 2007
TG101209, a small molecule JAK2-selective kinase inhibitor potently inhibits myeloproliferative disorder-associated JAK2V617F and MPLW515L/K mutations
A Pardanani, J Hood, T Lasho, et al.
Page
of 10