검색결과 : 8건
| No. | Article |
|---|---|
| 1 |
Human dihydrofolate reductase is a substrate of protein kinase CK2 alpha Skierka K, Wilamowski P, Wielechowska M, Cysewski D, Senkara E, Winska P, Bretner M, Ciesla J Biochemical and Biophysical Research Communications, 513(2), 368, 2019 |
| 2 |
Study of the physicochemical properties of protein kinase CK2 inhibitors -TBBt, TBBi and 2-Me-TBBi Lukowska-Chojnacka E, Pobudkowska A, Bretner M Fluid Phase Equilibria, 479, 52, 2019 |
| 3 |
Thermodynamic parameters for binding of some halogenated inhibitors of human protein kinase CK2 Winiewska M, Makowska M, Maj P, Wielechowska M, Bretner M, Poznanski J, Shugar D Biochemical and Biophysical Research Communications, 456(1), 282, 2015 |
| 4 |
Experimental (C-13 NMR) and theoretical (ab initio molecular orbital calculations) studies on the prototropic tautomerism of benzotriazole and some derivatives symmetrically substituted on the benzene ring Poznanski J, Najda A, Bretner M, Shugar D Journal of Physical Chemistry A, 111(28), 6501, 2007 |
| 5 |
Searching for a new anti-HCV therapy: Synthesis and properties of tropolone derivatives Boguszewska-Chachulska AM, Krawczyk M, Najda A, Kopanska K, Stankiewicz-Drogon A, Zagorski-Ostoja W, Bretner M Biochemical and Biophysical Research Communications, 341(2), 641, 2006 |
| 6 |
TBBz but not TBBt discriminates between two molecular forms of CK2 in vivo and its implications Zien P, Abramczyk O, Domanska K, Bretner M, Szyszka R Biochemical and Biophysical Research Communications, 312(3), 623, 2003 |
| 7 |
Selectivity of 4,5,6,7-tetrabromobenzimidazole as an ATP-competitive potent inhibitor of protein kinase CK2 from various sources Zien P, Bretner M, Zastapilo K, Szyszka R, Shugar D Biochemical and Biophysical Research Communications, 306(1), 129, 2003 |
| 8 |
H-1 NMR conformational study of a variety of alpha-anomers of C5-substituted 2'-deoxyuridines: Comparison to their antiherpetic beta counterparts Poznanski J, Felczak K, Bretner M, Kulikowski T, Remin M Biochemical and Biophysical Research Communications, 283(5), 1142, 2001 |