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Search results (9)

« Back to Publications

Bisulfite-free direct detection of 5-methylcytosine and 5-hydroxymethylcytosine at base resolution.

Liu Y. et al, (2019), Nat Biotechnol, 37, 424 - 429

Bisulfite-free and base-resolution analysis of 5-methylcytidine and 5-hydroxymethylcytidine in RNA with peroxotungstate.

Yuan F. et al, (2019), Chem Commun (Camb), 55, 2328 - 2331

TAPS: A bisulfite-free, base-resolution and quantitative sequencing method for cytosine modifications

Liu Y. et al, (2019), CANCER RESEARCH, 79

Creation of a Novel Class of Potent and Selective MutT Homologue 1 (MTH1) Inhibitors Using Fragment-Based Screening and Structure-Based Drug Design.

Rahm F. et al, (2018), J Med Chem, 61, 2533 - 2551

Benzoisoquinolinediones as Potent and Selective Inhibitors of BRPF2 and TAF1/TAF1L Bromodomains.

Bouché L. et al, (2017), J Med Chem, 60, 4002 - 4022

BET inhibition as a new strategy for the treatment of gastric cancer.

Montenegro RC. et al, (2016), Oncotarget, 7, 43997 - 44012

Cell line with endogenous EGFRvIII expression is a suitable model for research and drug development purposes.

Stec WJ. et al, (2016), Oncotarget, 7, 31907 - 31925

Identification and Development of 2,3-Dihydropyrrolo[1,2-a]quinazolin-5(1H)-one Inhibitors Targeting Bromodomains within the Switch/Sucrose Nonfermenting Complex.

Sutherell CL. et al, (2016), J Med Chem, 59, 5095 - 5101

CHARACTERIZATION OF THE MOLECULAR BIOLOGY OF EGFRVIII IN THE POPULATIONAL CONTEXT IN THE DK-MG CELL LINE

Stec WJ. et al, (2014), ANTICANCER RESEARCH, 34, 6186 - 6186