Caroline J. Springer
Alderley Park
Manchester, ENG, United Kingdom
Manchester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 26 publications
Expression of Concern: Inhibiting EGF Receptor or SRC Family Kinase Signaling Overcomes BRAF Inhibitor Resistance in Melanoma.
Journal: Cancer discovery
Published: December 18, 2025
Hijacking the MDM2 E3 Ligase with Novel BRD4-Targeting Proteolysis-Targeting Chimeras in Pancreatic Cancer Cells.
Journal: Chembiochem : a European journal of chemical biology
Published: February 12, 2025
Toward the Scale-Up of a Bicyclic Homopiperazine via Schmidt Rearrangement and Photochemical Oxaziridine Rearrangement in Continuous-Flow.
Journal: Organic process research & development
Published: August 05, 2020
Single-cell analysis defines a pancreatic fibroblast lineage that supports anti-tumor immunity.
Journal: Cancer cell
Published: July 28, 2020
The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers.
Journal: Annals of oncology : official journal of the European Society for Medical Oncology
Published: June 15, 2020
2-Aminomethylene-5-sulfonylthiazole Inhibitors of Lysyl Oxidase (LOX) and LOXL2 Show Significant Efficacy in Delaying Tumor Growth.
Journal: Journal of medicinal chemistry
Published: August 21, 2019
Author Correction: Lysyl oxidase drives tumour progression by trapping EGF receptors at the cell surface.
Journal: Nature communications
Published: July 20, 2019
Investigating the Contribution of Collagen to the Tumor Biomechanical Phenotype with Noninvasive Magnetic Resonance Elastography.
Journal: Cancer research
Published: June 10, 2019
Anti-metastatic Inhibitors of Lysyl Oxidase (LOX): Design and Structure-Activity Relationships.
Journal: Journal of medicinal chemistry
Published: May 10, 2019
Lysyl oxidase drives tumour progression by trapping EGF receptors at the cell surface.
Journal: Nature communications
Published: November 11, 2016
A novel protocol for the one-pot borylation/Suzuki reaction provides easy access to hinge-binding groups for kinase inhibitors.
Journal: Organic & biomolecular chemistry
Published: December 02, 2015
Last Updated: 09/26/2026