12 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
27983846	66	Highly Potent and Isoform Selective Dual Site Binding Tankyrase/Wnt Signaling Inhibitors That Increase Cellular Glucose Uptake and Have Antiproliferative Activity.	University of Bath
28001384	189	Structural Basis for Potency and Promiscuity in Poly(ADP-ribose) Polymerase (PARP) and Tankyrase Inhibitors.	Health & Science University
26706174	46	Development and structural analysis of adenosine site binding tankyrase inhibitors.	University of Oulu
26183543	87	Discovery of potent and selective nonplanar tankyrase inhibiting nicotinamide mimics.	University of Oulu
25847771	121	Towards small molecule inhibitors of mono-ADP-ribosyltransferases.	Karolinska Institutet
32511917	79	Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor.	University of Oslo
31381853	124	Discovery and Optimization of 2-Arylquinazolin-4-ones into a Potent and Selective Tankyrase Inhibitor Modulating Wnt Pathway Activity.	Merck Healthcare
30655950	116	Rational Design of Cell-Active Inhibitors of PARP10.	Oregon Health and Science University
30006177	103	4-(Phenoxy) and 4-(benzyloxy)benzamides as potent and selective inhibitors of mono-ADP-ribosyltransferase PARP10/ARTD10.	University of Oulu
29748053	87	Design, synthesis and evaluation of potent and selective inhibitors of mono-(ADP-ribosyl)transferases PARP10 and PARP14.	Mcdaniel College
29155568	29	Discovery of a Novel Series of Tankyrase Inhibitors by a Hybridization Approach.	Leibniz-Forschungsinstitut F�R Molekulare Pharmakologie (Fmp)
28495083	70	Design and synthesis of potent inhibitors of the mono(ADP-ribosyl)transferase, PARP14.	Mcdaniel College