Background/aim: Neuroblastoma is a common childhood cancer with poor survival for children with high-risk disease, and ongoing research to improve outcomes is needed. Patient-derived xenografts (PDX) and genetically engineered mouse models (GEMM) are reliable models for oncologic research; however, they are resource-intensive, expensive, and require significant expertise to develop and maintain. We developed an orthotopic xenograft murine model of neuroblastoma that utilizes cryopreserved banks of human neuroblastoma cell lines, requires minimal equipment, and is easily reproducible.
View Article and Find Full Text PDFObjective: To summarize research to understand the priorities of consumers with spinal cord injury (SCI) as related to neuroprosthesis.
Materials And Methods: This review is generated from results presented during a session at the 2008 Neural Interfaces Conference held in Cleveland, OH including presentations of research, observation of a panel discussion, and a case study.
Results: Understanding priorities of consumers living with SCI may help guide development of technology to potentially increase quality of life, confidence, and independence.