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Molecular Pathology : MP
|
July 31, 2002
Synthetic inhibitors of CDKs induce different responses in androgen sensitive and androgen insensitive prostatic cancer cell lines
J Mad'arová, M Lukesová, A Hlobilková, et al.
Neoplasma
|
July 5, 2002
Nuclear receptors in early hormone refractory prostate cancer and their relationship to apoptosis-related proteins
Z Kolár, P G Murray, J Madarova, et al.
Cellular and Molecular Life Sciences : CMLS
|
July 9, 2005
Antiproliferative activity of olomoucine II, a novel 2,6,9-trisubstituted purine cyclin-dependent kinase inhibitor
V Krystof, I W McNae, M D Walkinshaw, et al.
Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology
|
June 16, 2011
Frequency of BCR-ABL fusion transcripts in Serbian patients with chronic myeloid leukemia
B Todoric-Zivanovic, M Strnad, D Stamatovic, et al.
Plant Physiology and Biochemistry : PPB
|
April 2, 2014
Effect of light on growth and endogenous hormones in Chlorella minutissima (Trebouxiophyceae)
W A Stirk, P Bálint, D Tarkowská, et al.
Journal of Chemical Theory and Computation
|
June 29, 2019
Combined Small-Angle X-ray and Neutron Scattering Restraints in Molecular Dynamics Simulations
Po-Chia Chen, Roman Shevchuk, Felix M Strnad, et al.
Investigational New Drugs
|
January 19, 2000
A phase II trial of homoharringtonine and caracemide in the treatment of patients with advanced large bowel cancer
R S Witte, S Lipsitz, T L Goodman, et al.
European Journal of Biochemistry
|
September 1, 1994
Inhibition of cyclin-dependent kinases by purine analogues
J Veselý, L Havlicek, M Strnad, et al.
Organic & Biomolecular Chemistry
|
October 8, 2016
Design, synthesis and biological activities of new brassinosteroid analogues with a phenyl group in the side chain
M Kvasnica, J Oklestkova, V Bazgier, et al.
Physiological Research
|
March 1, 2021
In vitro and in silico studies of interaction of synthetic 2,6,9-trisubstituted purine kinase inhibitors BPA-302, BP-21 and BP-117 with liver drug-metabolizing cytochromes P450
A Špičáková, P Kraus, T Gucký, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Molecular Pathology : MP
|
July 31, 2002
Synthetic inhibitors of CDKs induce different responses in androgen sensitive and androgen insensitive prostatic cancer cell lines
J Mad'arová, M Lukesová, A Hlobilková, et al.
Neoplasma
|
July 5, 2002
Nuclear receptors in early hormone refractory prostate cancer and their relationship to apoptosis-related proteins
Z Kolár, P G Murray, J Madarova, et al.
Cellular and Molecular Life Sciences : CMLS
|
July 9, 2005
Antiproliferative activity of olomoucine II, a novel 2,6,9-trisubstituted purine cyclin-dependent kinase inhibitor
V Krystof, I W McNae, M D Walkinshaw, et al.
Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology
|
June 16, 2011
Frequency of BCR-ABL fusion transcripts in Serbian patients with chronic myeloid leukemia
B Todoric-Zivanovic, M Strnad, D Stamatovic, et al.
Plant Physiology and Biochemistry : PPB
|
April 2, 2014
Effect of light on growth and endogenous hormones in Chlorella minutissima (Trebouxiophyceae)
W A Stirk, P Bálint, D Tarkowská, et al.
Journal of Chemical Theory and Computation
|
June 29, 2019
Combined Small-Angle X-ray and Neutron Scattering Restraints in Molecular Dynamics Simulations
Po-Chia Chen, Roman Shevchuk, Felix M Strnad, et al.
Investigational New Drugs
|
January 19, 2000
A phase II trial of homoharringtonine and caracemide in the treatment of patients with advanced large bowel cancer
R S Witte, S Lipsitz, T L Goodman, et al.
European Journal of Biochemistry
|
September 1, 1994
Inhibition of cyclin-dependent kinases by purine analogues
J Veselý, L Havlicek, M Strnad, et al.
Organic & Biomolecular Chemistry
|
October 8, 2016
Design, synthesis and biological activities of new brassinosteroid analogues with a phenyl group in the side chain
M Kvasnica, J Oklestkova, V Bazgier, et al.
Physiological Research
|
March 1, 2021
In vitro and in silico studies of interaction of synthetic 2,6,9-trisubstituted purine kinase inhibitors BPA-302, BP-21 and BP-117 with liver drug-metabolizing cytochromes P450
A Špičáková, P Kraus, T Gucký, et al.
Page
of 9