| Autor: |
Sandeep S. Davé, David B. Dunson, Jyotishka Datta, Yuan Zhuang, Shawn Levy, Cassandra Love, Anupama Reddy, Deepthi Rajagopalan, Jenny Zhang, Guojie Li, Nicholas S. Davis, Randy D. Gascoyne, Sandra Basic-Kinda, Igor Aurer, John R. Goodlad, William W. L. Choi, Gopesh Srivastava, Rex K.H. Au-Yeung, Amy Chadburn, Andrew M. Evens, Monika Pilichowska, Pierre Sujobert, Anne Moreau, Marie Parrens, Lucile Baseggio, Mayur Parihar, Anne W. Beaven, Christopher R. Flowers, Leon Bernal-Mizrachi, Steven Horwitz, Neha Mehta-Shah, Wing C. Chan, Dennis Weisenburger, Lawrence Low, Eric D. Hsi, Sarah L. Ondrejka, Yuri Fedoriw, Kristy L. Richards, Jennifer R. Chapman-Fredricks, Izidore S. Lossos, Magdalena B. Czader, Virginie Fataccioli, Marie Helene Delfau-Larue, Karim Belhadj, Javeed Iqbal, Tayla Heavican, Liqiang Xi, Stefania Pittaluga, Elaine S. Jaffe, Mark Raffeld, Alina Nicolae, Laurence De Leval, Marion Travert, Philippe Gaulard, Andrea B. Moffitt, Matthew McKinney |
| Rok vydání: |
2023 |
| Popis: |
Supplementary Figure S1. Sanger sequencing chromatograms. Supplementary Figure S2. Cancer cell fraction for driver genes. Supplementary Figure S3. Ideogram with chromosome 7 alterations. Supplementary Figure S4. Examples of Exome Copy Number. Supplementary Figure S5. Exploratory Kaplan-Meier plots for clinical covariates. Supplementary Figure S6. Exploratory Kaplan-Meier plots for molecular covariates. Supplementary Figure S7. Sanger and exome sequencing validation of SETD2 biallelic mutation in one HSTL case. Supplementary Figure S8. SETD2 expression in mutant vs. wildtype cases. Supplementary Figure S9. Mutual exclusivity of STAT5B, PIK3CD, and STAT3 mutations. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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