Results 261 to 270 of about 21,005 (271)
Some of the next articles are maybe not open access.
Pediatric Myelodysplastic Syndrome with SF3B1 Mutation.
Journal of the Association of Genetic TechnologistsPatients with Fanconi Anemia (FA) have an increased risk of developing myeloid malignancies, which often precede the diagnosis of FA. We describe a patient with non-specific clinical findings diagnosed with myelodysplastic syndrome (MDS) at 17 years of age.
Britt, Boles +3 more
openaire +1 more source
Prevalence and clinical correlations of SF3B1 variants in lactotroph tumours.
European Journal of Endocrinology, 2023J. Simon +19 more
semanticscholar +1 more source
Uveal Melanomas with SF3B1 Mutations
Ophthalmology, 2016Serdar Yavuzyigitoglu +8 more
openaire +1 more source
Molecular determinants of survival in metastatic uveal melanoma: The impact of SF3B1 mutations.
European Journal of CancerL. D. del Carpio +11 more
semanticscholar +1 more source
CDK11 regulates pre-mRNA splicing by phosphorylation of SF3B1
Nature, 2022M. Hluchý +14 more
semanticscholar +1 more source
Inhibition of SF3B1 affects recruitment of P-TEFb to chromatin through multiple mechanisms
bioRxivGilbert Ansa +2 more
semanticscholar +1 more source

