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British Journal of Pharmacology
|
July 1, 1995
Pharmacological profile of the novel P2T-purinoceptor antagonist, FPL 67085 in vitro and in the anaesthetized rat in vivo
R G Humphries, W Tomlinson, J A Clegg, et al.
Nature
|
February 4, 1988
A new human immunoglobulin VH family preferentially rearranged in immature B-cell tumours
C G Humphries, A Shen, W A Kuziel, et al.
British Journal of Pharmacology
|
July 1, 1985
The effects of dopexamine on the cardiovascular system of the dog
R A Brown, J B Farmer, J C Hall, et al.
British Journal of Pharmacology
|
June 18, 1998
P2Y1-receptors in human platelets which are pharmacologically distinct from P2Y(ADP)-receptors
M S Fagura, I A Dainty, G D McKay, et al.
Oncotarget
|
September 15, 2016
The ubiquitin ligase TRIM25 targets ERG for degradation in prostate cancer
Shan Wang, Rahul K Kollipara, Caroline G Humphries, et al.
British Journal of Pharmacology
|
July 1, 1985
Dopexamine: a novel agonist at peripheral dopamine receptors and beta 2-adrenoceptors
R A Brown, J Dixon, J B Farmer, et al.
Cell Metabolism
|
September 30, 2014
Inhibition of cancer cell proliferation by PPARγ is mediated by a metabolic switch that increases reactive oxygen species levels
Nishi Srivastava, Rahul K Kollipara, Dinesh K Singh, et al.
The Journal of Pharmacy and Pharmacology
|
February 1, 1996
P2T purinoceptor antagonists. A QSAR study of some 2-substituted ATP analogues
N P Tomkinson, D P Marriott, P A Cage, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 18, 2003
Blockade of the platelet P2Y12 receptor by AR-C69931MX sustains coronary artery recanalization and improves the myocardial tissue perfusion in a canine thrombosis model
Kai Wang, Xiaorong Zhou, Zhongmin Zhou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2014
Ablation of the oncogenic transcription factor ERG by deubiquitinase inhibition in prostate cancer
Shan Wang, Rahul K Kollipara, Nishi Srivastava, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
British Journal of Pharmacology
|
July 1, 1995
Pharmacological profile of the novel P2T-purinoceptor antagonist, FPL 67085 in vitro and in the anaesthetized rat in vivo
R G Humphries, W Tomlinson, J A Clegg, et al.
Nature
|
February 4, 1988
A new human immunoglobulin VH family preferentially rearranged in immature B-cell tumours
C G Humphries, A Shen, W A Kuziel, et al.
British Journal of Pharmacology
|
July 1, 1985
The effects of dopexamine on the cardiovascular system of the dog
R A Brown, J B Farmer, J C Hall, et al.
British Journal of Pharmacology
|
June 18, 1998
P2Y1-receptors in human platelets which are pharmacologically distinct from P2Y(ADP)-receptors
M S Fagura, I A Dainty, G D McKay, et al.
Oncotarget
|
September 15, 2016
The ubiquitin ligase TRIM25 targets ERG for degradation in prostate cancer
Shan Wang, Rahul K Kollipara, Caroline G Humphries, et al.
British Journal of Pharmacology
|
July 1, 1985
Dopexamine: a novel agonist at peripheral dopamine receptors and beta 2-adrenoceptors
R A Brown, J Dixon, J B Farmer, et al.
Cell Metabolism
|
September 30, 2014
Inhibition of cancer cell proliferation by PPARγ is mediated by a metabolic switch that increases reactive oxygen species levels
Nishi Srivastava, Rahul K Kollipara, Dinesh K Singh, et al.
The Journal of Pharmacy and Pharmacology
|
February 1, 1996
P2T purinoceptor antagonists. A QSAR study of some 2-substituted ATP analogues
N P Tomkinson, D P Marriott, P A Cage, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 18, 2003
Blockade of the platelet P2Y12 receptor by AR-C69931MX sustains coronary artery recanalization and improves the myocardial tissue perfusion in a canine thrombosis model
Kai Wang, Xiaorong Zhou, Zhongmin Zhou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2014
Ablation of the oncogenic transcription factor ERG by deubiquitinase inhibition in prostate cancer
Shan Wang, Rahul K Kollipara, Nishi Srivastava, et al.
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of 4