BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 18258654)

  • 21. Optimization of protein kinase CK2 inhibitors derived from 4,5,6,7-tetrabromobenzimidazole.
    Pagano MA; Andrzejewska M; Ruzzene M; Sarno S; Cesaro L; Bain J; Elliott M; Meggio F; Kazimierczuk Z; Pinna LA
    J Med Chem; 2004 Dec; 47(25):6239-47. PubMed ID: 15566294
    [TBL] [Abstract][Full Text] [Related]  

  • 22. CK2α and CK2α' subunits differ in their sensitivity to 4,5,6,7-tetrabromo- and 4,5,6,7-tetraiodo-1H-benzimidazole derivatives.
    Janeczko M; Orzeszko A; Kazimierczuk Z; Szyszka R; Baier A
    Eur J Med Chem; 2012 Jan; 47(1):345-50. PubMed ID: 22115617
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Characterization of ATM and DNA-PK wild-type and mutant cell lines upon DSB induction in the presence and absence of CK2 inhibitors.
    Olsen BB; Fritz G; Issinger OG
    Int J Oncol; 2012 Feb; 40(2):592-8. PubMed ID: 21993375
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Major tegument protein VP8 of bovine herpesvirus 1 is phosphorylated by viral US3 and cellular CK2 protein kinases.
    Labiuk SL; Babiuk LA; van Drunen Littel-van den Hurk S
    J Gen Virol; 2009 Dec; 90(Pt 12):2829-2839. PubMed ID: 19692545
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Biological properties and structural study of new aminoalkyl derivatives of benzimidazole and benzotriazole, dual inhibitors of CK2 and PIM1 kinases.
    Chojnacki K; Wińska P; Wielechowska M; Łukowska-Chojnacka E; Tölzer C; Niefind K; Bretner M
    Bioorg Chem; 2018 Oct; 80():266-275. PubMed ID: 29966873
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Toward the rational design of protein kinase casein kinase-2 inhibitors.
    Sarno S; Moro S; Meggio F; Zagotto G; Dal Ben D; Ghisellini P; Battistutta R; Zanotti G; Pinna LA
    Pharmacol Ther; 2002; 93(2-3):159-68. PubMed ID: 12191608
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Dynamic regulation of a metabolic multi-enzyme complex by protein kinase CK2.
    An S; Kyoung M; Allen JJ; Shokat KM; Benkovic SJ
    J Biol Chem; 2010 Apr; 285(15):11093-9. PubMed ID: 20157113
    [TBL] [Abstract][Full Text] [Related]  

  • 28. p53 is dispensable for the induction of apoptosis after inhibition of protein kinase CK2.
    Schneider CC; Hessenauer A; Montenarh M; Götz C
    Prostate; 2010 Feb; 70(2):126-34. PubMed ID: 19760628
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Halogenated imidazole derivatives block RNA polymerase II elongation along mitogen inducible genes.
    Mikula M; Hanusek K; Paziewska A; Dzwonek A; Rubel T; Bomsztyk K; Ostrowski J
    BMC Mol Biol; 2010 Jan; 11():4. PubMed ID: 20078881
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Functional proteomics strategy for validation of protein kinase inhibitors reveals new targets for a TBB-derived inhibitor of protein kinase CK2.
    Gyenis L; Kuś A; Bretner M; Litchfield DW
    J Proteomics; 2013 Apr; 81():70-9. PubMed ID: 23017496
    [TBL] [Abstract][Full Text] [Related]  

  • 31. TBBz but not TBBt discriminates between two molecular forms of CK2 in vivo and its implications.
    Zień P; Abramczyk O; Domańska K; Bretner M; Szyszka R
    Biochem Biophys Res Commun; 2003 Dec; 312(3):623-8. PubMed ID: 14680810
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A subnanomolar fluorescent probe for protein kinase CK2 interaction studies.
    Enkvist E; Viht K; Bischoff N; Vahter J; Saaver S; Raidaru G; Issinger OG; Niefind K; Uri A
    Org Biomol Chem; 2012 Nov; 10(43):8645-53. PubMed ID: 23032938
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inhibition of experimental HCC growth in mice by use of the kinase inhibitor DMAT.
    Sass G; Klinger N; Sirma H; Hashemolhosseini S; Hellerbrand C; Neureiter D; Wege H; Ocker M; Tiegs G
    Int J Oncol; 2011 Aug; 39(2):433-42. PubMed ID: 21567083
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Tetrabromocinnamic acid (TBCA) and related compounds represent a new class of specific protein kinase CK2 inhibitors.
    Pagano MA; Poletto G; Di Maira G; Cozza G; Ruzzene M; Sarno S; Bain J; Elliott M; Moro S; Zagotto G; Meggio F; Pinna LA
    Chembiochem; 2007 Jan; 8(1):129-39. PubMed ID: 17133643
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Synthesis of new analogs of benzotriazole, benzimidazole and phthalimide--potential inhibitors of human protein kinase CK2.
    Najda-Bernatowicz A; Łebska M; Orzeszko A; Kopańska K; Krzywińska E; Muszyńska G; Bretner M
    Bioorg Med Chem; 2009 Feb; 17(4):1573-8. PubMed ID: 19168362
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Too much of a good thing: the role of protein kinase CK2 in tumorigenesis and prospects for therapeutic inhibition of CK2.
    Duncan JS; Litchfield DW
    Biochim Biophys Acta; 2008 Jan; 1784(1):33-47. PubMed ID: 17931986
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Synthesis of novel polybrominated benzimidazole derivatives-potential CK2 inhibitors with anticancer and proapoptotic activity.
    Łukowska-Chojnacka E; Wińska P; Wielechowska M; Poprzeczko M; Bretner M
    Bioorg Med Chem; 2016 Feb; 24(4):735-41. PubMed ID: 26778657
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Design and synthesis of CK2 inhibitors.
    Makowska M; Łukowska-Chojnacka E; Wińska P; Kuś A; Bilińska-Chomik A; Bretner M
    Mol Cell Biochem; 2011 Oct; 356(1-2):91-6. PubMed ID: 21750983
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Selectivity of 4,5,6,7-tetrabromobenzimidazole as an ATP-competitive potent inhibitor of protein kinase CK2 from various sources.
    Zień P; Bretner M; Zastapiło K; Szyszka R; Shugar D
    Biochem Biophys Res Commun; 2003 Jun; 306(1):129-33. PubMed ID: 12788077
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Synthesis, biological properties and structural study of new halogenated azolo[4,5-b]pyridines as inhibitors of CK2 kinase.
    Chojnacki K; Lindenblatt D; Wińska P; Wielechowska M; Toelzer C; Niefind K; Bretner M
    Bioorg Chem; 2021 Jan; 106():104502. PubMed ID: 33317841
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.