Rogier C. Buijsman
Oss, NB, Netherlands
Last Updated: 09/26/2026
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Found 27 publications
Dual TTK/PLK1 inhibition has potent anticancer activity in TNBC as monotherapy and in combination.
Journal: Frontiers in oncology
Published: June 12, 2024
Screening of predicted synergistic multi-target therapies in glioblastoma identifies new treatment strategies.
Journal: Neuro-oncology advances
Published: July 17, 2023
Minifragment plating of the fibula in unstable ankle fractures.
Journal: Archives of orthopaedic and trauma surgery
Published: November 22, 2021
LCK inhibition downregulates YAP activity and is therapeutic in patient-derived models of cholangiocarcinoma.
Journal: Journal of hepatology
Published: October 06, 2021
Targeting Indoleamine 2,3-Dioxygenase in Cancer Models Using the Novel Small Molecule Inhibitor NTRC 3883-0.
Journal: Frontiers in immunology
Published: September 23, 2020
Pharmacological validation of TDO as a target for Parkinson's disease.
Journal: The FEBS journal
Published: September 11, 2020
Mapping Arginase Expression with 18F-Fluorinated Late-Generation Arginase Inhibitors Derived from Quaternary α-Amino Acids.
Journal: Journal of nuclear medicine : official publication, Society of Nuclear Medicine
Published: August 11, 2020
High-Throughput Fluorescence-Based Activity Assay for Arginase-1.
Journal: SLAS discovery : advancing life sciences R & D
Published: May 19, 2020
Chemotherapy sensitivity testing on ovarian cancer cells isolated from malignant ascites.
Journal: Oncotarget
Published: April 08, 2020
Structural insights into human Arginase-1 pH dependence and its inhibition by the small molecule inhibitor CB-1158.
Journal: Journal of structural biology: X
Published: October 19, 2019
Combined Cellular and Biochemical Profiling to Identify Predictive Drug Response Biomarkers for Kinase Inhibitors Approved for Clinical Use between 2013 and 2017.
Journal: Molecular cancer therapeutics
Published: August 03, 2018
Design, Synthesis, and Biological Evaluation of Novel Type I1/2 p38α MAP Kinase Inhibitors with Excellent Selectivity, High Potency, and Prolonged Target Residence Time by Interfering with the R-Spine.
Journal: Journal of medicinal chemistry
Published: August 24, 2017
Last Updated: 09/26/2026