/
/
מידול אוסטאוסרקומה באמצעות תאי גזע Pluripotent נגזר החולה המושרה תסמונת לי-פראומני, היא תורשתית
É necessária uma assinatura da JoVE para visualizar este conteúdo. Faça login ou comece sua avaliação gratuita.
1Department of Integrative Biology and Pharmacology, McGovern Medical School,The University of Texas Health Science Center at Houston, 2Graduate School of Biomedical Sciences,The University of Texas MD Anderson Cancer Center UTHealth, 3Department of Musculoskeletal Oncology,The First Affiliated Hospital of Sun Yat-sen University, 4Women’s Health Institute,Cleveland Clinic Foundation, 5Center for Stem Cell and Regenerative Medicine, The Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases,The University of Texas Health Science Center at Houston, 6Center for Precision Health, School of Biomedical Informatics and School of Public Health,The University of Texas Health Science Center at Houston
Capítulos
- 00:04Título
- 00:47Differentiation of Li-Fraumeni Syndrome (LFS) Patient-derived Induced Pluripotent Stem Cell (iPSC) to Mesenchymal Stem Cell (MSC) (Days 0 – 28)
- 02:19iPSC-derived MSC Maturation (Day 28 – 45) and Differentiation of LFS MSC to Osteoblasts (Day 0 – 24)
- 04:33Xenograft In Vivo Tumorigenesis Model Setup
- 06:39Results: Representative LFS MSC Differentiation
- 08:10Conclusion
