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Prognostic interaction between bone marrow morphology and SF3B1 (Montrer SF3B2 Protéines) and ASXL1 (Montrer ASXL1 Protéines) mutations in myelodysplastic syndromes with ring sideroblasts.
SF3B1 (Montrer SF3B2 Protéines) mutations were also associated with del(11q), which is prognostically different from inv (Montrer INVS Protéines)(3)(q21q26.2)
Results find that SF3B1 (Montrer SF3B2 Protéines) retained intron 4 (i4) harbors cryptic exons that are highly conserved and decoy exon E4e can promote intron retention at heterologous sites.
Integrated ERK1 (Montrer MAPK3 Protéines)/ERK2 (Montrer MAPK1 Protéines) response to B (Montrer TDO2 Protéines)-cell receptor stimulation and SF3B1 (Montrer SF3B2 Protéines) gene mutations refine prognosis in chronic lymphocytic leukemia.
could confirm the very good prognosis of MDS (Montrer PAFAH1B1 Protéines) patients with del(11q) as described in the IPSS-R and identified a very high frequency of SF3B1 (Montrer SF3B2 Protéines) mutations, a relatively low ASXL1 (Montrer ASXL1 Protéines) and TP53 (Montrer TP53 Protéines) mutation frequency, as well as a lack of EZH2 (Montrer EZH2 Protéines) mutations as possible molecular reason for this favorable outcome
Our findings suggest that the genetic profile of coexistent GNAQ (Montrer GNAQ Protéines) or GNA11 (Montrer GNA11 Protéines) mutations with BAP1 (Montrer RNF2 Protéines) or SF3B1 (Montrer SF3B2 Protéines) mutations can aid the histopathological diagnosis of blue nevus-like melanoma and distinguish blue nevus-like melanoma from conventional epidermal-derived melanomas.
Mutation in SF3B1 (Montrer SF3B2 Protéines) gene is associated with mucosal melanoma.
These data provide a catalog of copy-number associated gene dependencies and identify partial copy-loss of wild-type SF3B1 (Montrer SF3B2 Protéines) as a novel, non-driver cancer gene dependency.
although blocking the function of SF3b elicits a massive accumulation of unspliced pre-mRNAs in the nucleus, intron-containing transcripts can still bind the ALYREF (Montrer THOC4 Protéines) export factor and be transported to the cytoplasm, where they trigger an alternative nonsense-mediated decay pathway.
this study shows that DNMT3A (Montrer DNMT3A Protéines) mutations are present in a significant proportion of SF3B1mut patients with RARS (Montrer RARS Protéines) and its presence has a clearly negative impact on outcomes, determining a higher RBC (Montrer CACNA1C Protéines) transfusion dependency, higher risk of progression to AML (Montrer RUNX1 Protéines), and lower OS.
Our findings demonstrate that, despite significant differences in affected transcripts, there is overlap in the phenotypes associated with SF3B1-K700E between human and mouse.
Sf3b1(K700E) mice develop macrocytic anemia (Montrer TCN2 Protéines) due to a terminal erythroid maturation defect, erythroid dysplasia, and long-term hematopoietic stem cell (LT-HSC (Montrer FUT1 Protéines)) expansion.
myocardial hypoxia actuates fructose metabolism in human and mouse models of pathological cardiac hypertrophy through hypoxia-inducible factor 1alpha (HIF1alpha (Montrer HIF1A Protéines)) activation of SF3B1 and SF3B1-mediated splice switching of KHK (Montrer KHK Protéines)-A to KHK (Montrer KHK Protéines)-C
Sf3b1 isrequired for the blastocyst formation.
SF3B1 plays an important role in the regulation of hematopoietic stem cells, whereas SF3B1 haploinsufficiency itself is not associated with the myelodysplastic syndrome phenotype with ring sideroblasts.
The level of Sf3b1 expression is critical for the proliferative capacity of hematopoietic stem cells. Depletion of Sf3b1 impairs proliferative capacity of hematopoietic stem cells but is not sufficient to induce myelodysplasia.
SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes.
the active spliceosome, containing SAP155 phosphorylated by DYRKIA, performs pre-mRNA splicing in spermatogonia during testicular development
active spliceosome, containing phosphorylated SAP155, performs pre-mRNA splicing on chromatin concomitant with transcription during testicular development.
Sf3b1 and Polycomb (Montrer CBX2 Protéines) group (PcG) proteins interaction is essential for true PcG-mediated repression of Hox (Montrer MSH2 Protéines) genes.
Data indicate that splicing factor 3b (Montrer SF3B14 Protéines), subunit 1 (sf3b1) mutation causes aberrant splicing of sf3b1 resulting in functional and predicted non-functional transcripts and a 90% reduction in full-length Sf3b1 protein.
This gene encodes subunit 1 of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence independent manner and may anchor the U2 snRNP to the pre-mRNA. Splicing factor 3b is also a component of the minor U12-type spliceosome. The carboxy-terminal two-thirds of subunit 1 have 22 non-identical, tandem HEAT repeats that form rod-like, helical structures. Alternative splicing results in multiple transcript variants encoding different isoforms.
, pre-mRNA processing 10
, pre-mRNA splicing factor SF3b, 155 kDa subunit
, spliceosome-associated protein 155
, splicing factor 3B subunit 1
, pre-mRNA-splicing factor SF3b 155 kDa subunit
, splicing factor 3b, subunit 1, 155 kDa
, transforming growth factor alpha regulated gene 4
, 146 kDa nuclear protein
, splicing factor 3b, subunit 1, 155kDa
, splicing factor 3B subunit 1-like
, splicing factor 3b, subunit 1, 155kD