Cargando…
Integrated Genomic and Transcriptomic Analysis Improves Disease Classification and Risk Stratification of MDS with Ring Sideroblasts
PURPOSE: Ring sideroblasts (RS) define the low-risk myelodysplastic neoplasm (MDS) subgroup with RS but may also reflect erythroid dysplasia in higher risk myeloid neoplasm. The benign behavior of MDS with RS (MDS(RS+)) is limited to SF3B1-mutated cases without additional high-risk genetic events, b...
Autores principales: | Todisco, Gabriele, Creignou, Maria, Bernard, Elsa, Björklund, Ann-Charlotte, Moura, Pedro Luis, Tesi, Bianca, Mortera-Blanco, Teresa, Sander, Birgitta, Jansson, Monika, Walldin, Gunilla, Barbosa, Indira, Reinsbach, Susanne E., Hofman, Isabel Juliana, Nilsson, Christer, Yoshizato, Tetsuichi, Dimitriou, Marios, Chang, David, Olafsdottir, Svannildur, Venckute Larsson, Sigita, Tobiasson, Magnus, Malcovati, Luca, Woll, Petter, Jacobsen, Sten Eirik W., Papaemmanuil, Elli, Hellström-Lindberg, Eva |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for Cancer Research
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570683/ https://www.ncbi.nlm.nih.gov/pubmed/37498312 http://dx.doi.org/10.1158/1078-0432.CCR-23-0538 |
Ejemplares similares
-
The extent of residual WT HSPCs is associated with the degree of anemia in patients with SF3B1-mutated MDS-RS
por: Hofman, Isabel Juliana F., et al.
Publicado: (2022) -
P713: EXPLORING CLONAL COMPETITION THROUGH 12-YEAR FOLLOW-UP OF AN MDS-RS PATIENT WITH DUAL SF3B1 MUTATIONS
por: Moura, Pedro, et al.
Publicado: (2023) -
Aberrant splicing of genes involved in haemoglobin synthesis and impaired terminal erythroid maturation in SF3B1 mutated refractory anaemia with ring sideroblasts
por: Conte, Simona, et al.
Publicado: (2015) -
Clinical and genetic characteristics of congenital sideroblastic anemia: comparison with myelodysplastic syndrome with ring sideroblast (MDS-RS)
por: Ohba, Rie, et al.
Publicado: (2012) -
Perturbed hematopoietic stem and progenitor cell hierarchy in myelodysplastic syndromes patients with monosomy 7 as the sole cytogenetic abnormality
por: Dimitriou, Marios, et al.
Publicado: (2016)