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 Technologists
Patients 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, 2023
J. Simon   +19 more
semanticscholar   +1 more source

Anti-Sf3b1

Hybridoma and Hybridomics, 2003
openaire   +1 more source

3220 – SF3B1/DNMT3A CO-MUTATION MIMICS FEATURES OF SOLE SF3B1 OR DNMT3A MUTATION DEPENDING ON STRESS CONDITIONS

Experimental Hematology, 2022
LaShanale Wallace   +9 more
openaire   +1 more source

Uveal Melanomas with SF3B1 Mutations

Ophthalmology, 2016
Serdar Yavuzyigitoglu   +8 more
openaire   +1 more source

Molecular determinants of survival in metastatic uveal melanoma: The impact of SF3B1 mutations.

European Journal of Cancer
L. D. del Carpio   +11 more
semanticscholar   +1 more source

CDK11 regulates pre-mRNA splicing by phosphorylation of SF3B1

Nature, 2022
M. Hluchý   +14 more
semanticscholar   +1 more source

The splicing factor SF3B1 confers ferroptosis resistance and promotes lung adenocarcinoma progression via upregulation of SLC7A11

Cancer Gene Therapy
Yanlin Guo   +15 more
semanticscholar   +1 more source

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