Abstract
No public abstract is available from the verified source records.
Pedro Luis Moura, Yasuhito Nannya, Affaf Aliouat, Isabel Juliana Hofman, Teresa Mortera-Blanco, Tetsuichi Yoshizato, Ryunosuke Saiki, Masahiro M. Nakagawa, Maria Creignou, Ann-Charlotte Björklund, Gunilla Walldin, Indira Barbosa, Monika Jansson, Francesca Grasso, Edda M. Elvarsdottir, Petter S. Woll, Sten Eirik W. Jacobsen, Seishi Ogawa, Eva Hellström-Lindberg
Abstract
Authors
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The spliceosome: design principles of a dynamic RNP machine
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crossref
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pubmed
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europepmc
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unpaywall
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datacite
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TARGET-seq: a protocol for high-sensitivity single-cell mutational analysis and parallel RNA sequencing
2020
The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts
10.1038/leu.2012.298 · 2013
Iron overload impairs normal hematopoietic stem and progenitor cells through reactive oxygen species and shortens survival in myelodysplastic syndrome mice
10.3324/haematol.2018.193128 · 2018
High-throughput transcription profiling identifies putative epigenetic regulators of hematopoiesis
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Mutations in CHD2 cause defective association with active chromatin in chronic lymphocytic leukemia
10.1182/blood-2014-10-604959 · 2015
Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations
10.1182/blood-2018-04-843771 · 2018
A nuclear cap binding protein complex involved in pre-mRNA splicing
10.1016/0092-8674(94)90530-4 · 1994
SNW1 enables sister chromatid cohesion by mediating the splicing of sororin and APC2 pre-mRNAs
10.15252/embj.201488202 · 2014
METTL3-mediated m6A modification controls splicing factor abundance and contributes to aggressive CLL
10.1158/2643-3230.bcd-22-0156 · 2023
Mga, a dual-specificity transcription factor that interacts with Max and contains a T-domain DNA-binding motif
10.1093/emboj/18.24.7019 · 1999
PHF20L1 as a H3K27me2 reader coordinates with transcriptional repressors to promote breast tumorigenesis
10.1126/sciadv.aaz0356 · 2020
Single-cell genomics reveals the genetic and molecular bases for escape from mutational epistasis in myeloid neoplasms
10.1182/blood.2020006868 · 2020
SF3B1 mutations induce R-loop accumulation and DNA damage in MDS and leukemia cells with therapeutic implications
10.1038/s41375-020-0753-9 · 2020
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