BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 29769258)

  • 41. Global target profile of the kinase inhibitor bosutinib in primary chronic myeloid leukemia cells.
    Remsing Rix LL; Rix U; Colinge J; Hantschel O; Bennett KL; Stranzl T; Müller A; Baumgartner C; Valent P; Augustin M; Till JH; Superti-Furga G
    Leukemia; 2009 Mar; 23(3):477-85. PubMed ID: 19039322
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Deciphering targeting rules of splicing modulator compounds: case of TG003.
    Sakuma M; Iida K; Hagiwara M
    BMC Mol Biol; 2015 Sep; 16():16. PubMed ID: 26400733
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Two nucleus-localized CDK-like kinases with crucial roles for malaria parasite erythrocytic replication are involved in phosphorylation of splicing factor.
    Agarwal S; Kern S; Halbert J; Przyborski JM; Baumeister S; Dandekar T; Doerig C; Pradel G
    J Cell Biochem; 2011 May; 112(5):1295-310. PubMed ID: 21312235
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Effect of AKT3 expression on MYC- and caspase-8-dependent apoptosis caused by polo-like kinase inhibitors in HCT 116 cells.
    Nonomiya Y; Noguchi K; Tanaka N; Kasagaki T; Katayama K; Sugimoto Y
    Cancer Sci; 2016 Dec; 107(12):1877-1887. PubMed ID: 27699933
    [TBL] [Abstract][Full Text] [Related]  

  • 45. DYRK2 priming phosphorylation of c-Jun and c-Myc modulates cell cycle progression in human cancer cells.
    Taira N; Mimoto R; Kurata M; Yamaguchi T; Kitagawa M; Miki Y; Yoshida K
    J Clin Invest; 2012 Mar; 122(3):859-72. PubMed ID: 22307329
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Regulation of alternative pre-mRNA splicing by the ERK MAP-kinase pathway.
    Weg-Remers S; Ponta H; Herrlich P; König H
    EMBO J; 2001 Aug; 20(15):4194-203. PubMed ID: 11483522
    [TBL] [Abstract][Full Text] [Related]  

  • 47. PDK1 signaling toward PLK1-MYC activation confers oncogenic transformation, tumor-initiating cell activation, and resistance to mTOR-targeted therapy.
    Tan J; Li Z; Lee PL; Guan P; Aau MY; Lee ST; Feng M; Lim CZ; Lee EY; Wee ZN; Lim YC; Karuturi RK; Yu Q
    Cancer Discov; 2013 Oct; 3(10):1156-71. PubMed ID: 23887393
    [TBL] [Abstract][Full Text] [Related]  

  • 48. IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling.
    Sheng X; Nenseth HZ; Qu S; Kuzu OF; Frahnow T; Simon L; Greene S; Zeng Q; Fazli L; Rennie PS; Mills IG; Danielsen H; Theis F; Patterson JB; Jin Y; Saatcioglu F
    Nat Commun; 2019 Jan; 10(1):323. PubMed ID: 30679434
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Leucettine L41, a DYRK1A-preferential DYRKs/CLKs inhibitor, prevents memory impairments and neurotoxicity induced by oligomeric Aβ25-35 peptide administration in mice.
    Naert G; Ferré V; Meunier J; Keller E; Malmström S; Givalois L; Carreaux F; Bazureau JP; Maurice T
    Eur Neuropsychopharmacol; 2015 Nov; 25(11):2170-82. PubMed ID: 26381812
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Pyrido[2,3-d]pyrimidines: discovery and preliminary SAR of a novel series of DYRK1B and DYRK1A inhibitors.
    Anderson K; Chen Y; Chen Z; Dominique R; Glenn K; He Y; Janson C; Luk KC; Lukacs C; Polonskaia A; Qiao Q; Railkar A; Rossman P; Sun H; Xiang Q; Vilenchik M; Wovkulich P; Zhang X
    Bioorg Med Chem Lett; 2013 Dec; 23(24):6610-5. PubMed ID: 24239188
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Benzobisthiazoles Represent a Novel Scaffold for Kinase Inhibitors of CLK Family Members.
    Prak K; Kriston-Vizi J; Chan AW; Luft C; Costa JR; Pengo N; Ketteler R
    Biochemistry; 2016 Jan; 55(3):608-17. PubMed ID: 26701387
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Deregulated Syk inhibits differentiation and induces growth factor-independent proliferation of pre-B cells.
    Wossning T; Herzog S; Köhler F; Meixlsperger S; Kulathu Y; Mittler G; Abe A; Fuchs U; Borkhardt A; Jumaa H
    J Exp Med; 2006 Dec; 203(13):2829-40. PubMed ID: 17130299
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Identification of CLK1 Inhibitors by a Fragment-linking Based Virtual Screening.
    Walter A; Chaikuad A; Loaëc N; Preu L; Knapp S; Meijer L; Kunick C; Koch O
    Mol Inform; 2017 Apr; 36(4):. PubMed ID: 28000414
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Marine-Derived 2-Aminoimidazolone Alkaloids. Leucettamine B-Related Polyandrocarpamines Inhibit Mammalian and Protozoan DYRK & CLK Kinases.
    Loaëc N; Attanasio E; Villiers B; Durieu E; Tahtouh T; Cam M; Davis RA; Alencar A; Roué M; Bourguet-Kondracki ML; Proksch P; Limanton E; Guiheneuf S; Carreaux F; Bazureau JP; Klautau M; Meijer L
    Mar Drugs; 2017 Oct; 15(10):. PubMed ID: 29039762
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Phosphorylation of CLK2 at serine 34 and threonine 127 by AKT controls cell survival after ionizing radiation.
    Nam SY; Seo HH; Park HS; An S; Kim JY; Yang KH; Kim CS; Jeong M; Jin YW
    J Biol Chem; 2010 Oct; 285(41):31157-63. PubMed ID: 20682768
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Exploring the roles of the Cdc2-like kinases in cancers.
    Blackie AC; Foley DJ
    Bioorg Med Chem; 2022 Sep; 70():116914. PubMed ID: 35872347
    [TBL] [Abstract][Full Text] [Related]  

  • 57. SRPK1 and Clk/Sty protein kinases show distinct substrate specificities for serine/arginine-rich splicing factors.
    Colwill K; Feng LL; Yeakley JM; Gish GD; Cáceres JF; Pawson T; Fu XD
    J Biol Chem; 1996 Oct; 271(40):24569-75. PubMed ID: 8798720
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Mobilization of a splicing factor through a nuclear kinase-kinase complex.
    Aubol BE; Keshwani MM; Fattet L; Adams JA
    Biochem J; 2018 Feb; 475(3):677-690. PubMed ID: 29335301
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Prolactin induces c-Myc expression and cell survival through activation of Src/Akt pathway in lymphoid cells.
    Domínguez-Cáceres MA; García-Martínez JM; Calcabrini A; González L; Porque PG; León J; Martín-Pérez J
    Oncogene; 2004 Sep; 23(44):7378-90. PubMed ID: 15286700
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Synthesis of N,N'-bis(5-arylidene-4-oxo-3,5-dihydro-4H-imidazol-2-yl)diamines bearing various linkers and biological evaluation as potential inhibitors of kinases.
    Coulibaly WK; Paquin L; Bénie A; Bekro YA; Durieu E; Meijer L; Bazureau JP
    Eur J Med Chem; 2012 Dec; 58():581-90. PubMed ID: 23174317
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.