Machine learning for rhabdomyosarcoma histopathology
Correctly diagnosing a rare childhood cancer such as sarcoma can [...]
Preclinical therapeutics ex ovo quail eggs as a biomimetic automation-ready xenograft platform
Preclinical cancer research ranges from in vitro studies that are [...]
Bromodomain 4 inhibition leads to MYCN downregulation in Wilms tumor
Wilms tumor is the most common childhood kidney cancer. Two [...]
Probabilistic Boolean Modeling of Pre-clinical Tumor Models for Biomarker Identification in Cancer Drug Development
As high-throughput sequencing experiments become more widely used in pre-clinical [...]
Design considerations of an IL13Rα2 antibody-drug conjugate for difuse intrinsic pontine glioma
Diffuse intrinsic pontine glioma (DIPG), a rare pediatric brain tumor, [...]
Functional impact of a germline RET mutation in alveolar rhabdomyosarcoma
Specific mutations in the RET proto-oncogene are associated with multiple [...]
Receptor-driven invasion profiles in diffuse intrinsic pontine glioma
Diffuse intrinsic pontine glioma (DIPG) is a devastating pediatric cancer [...]
Defining the Extracellular Matrix of Rhabdomyosarcoma
Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood [...]
Refractory alveolar rhabdomyosarcoma in an 11-year-old male
Rhabdomyosarcoma (RMS) is a mesenchymal malignancy phenocopying muscle and is [...]
In vitro benchmarking of NF-κB inhibitors.
Rhabdomyosarcoma (RMS) is a mesenchymal malignancy phenocopying muscle and is [...]