Supplementary Tables 1-6 from Patient-Derived iPSCs Faithfully Represent the Genetic Diversity and Cellular Architecture of Human Acute Myeloid Leukemia

Autor: Eirini P. Papapetrou, Dan Hasson, Michael G. Kharas, Hanzhi Luo, Ravindra Majeti, Mark P. Chao, Elsa Bernard, Chan-Jung Chang, Deniz Demircioglu, Tiansu Wang, Malgorzata Olszewska, Nataly Cruz-Rodriguez, Saul Carcamo, Andriana G. Kotini
Rok vydání: 2023
DOI: 10.1158/2643-3230.22645264
Popis: Table S1. Patient characteristics. AML: acute myeloid leukemia; MDS: myelodysplastic syndrome; MPN: myeloproliferative neoplasm; ET: essential thrombocythemia; PBMCs: peripheral blood mononuclear cells; BMMCs: bone marrow mononuclear cells; PDX: patient-derived xenografts Table S2. All patient samples used in this study with genetic characterization and reprogramming outcomes. Blue font denotes partially reprogrammed (as opposed to bona fide iPSC) colonies and clones. Table S3. All AML-iPSC lines phenotypically characterized. Table S4. Top 50 upregulated genes (highest log2 fold change) in each cluster. Table S5. Primers used for genotyping. Table S6. Primers used for qRT-PCR analyses.
Databáze: OpenAIRE