Sf3b1 - Open Access .click

Results 161 to 170 of about 9,852 (179)

Some of the next articles are maybe not open access.

Pathologic Spectrum and Molecular Landscape of Myeloid Disorders Harboring SF3B1 Mutations

American Journal of Clinical Pathology, 2021
Rong He, Mrinal Patnaik, Jennifer L Herrick +2 more
exaly

Mutant SF3B1 splices a more leukemogenic EVI1

Blood, 2022
openaire +2 more sources

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

Transcriptomic Characterization of SF3B1 Mutation Reveals Its Pleiotropic Effects in Chronic Lymphocytic Leukemia

Cancer Cell, 2016
Shanye Yin, Thomas Kipps, David Deluca +2 more
exaly

A Murine Model of Chronic Lymphocytic Leukemia Based on B Cell-Restricted Expression of Sf3b1 Mutation and Atm Deletion

Cancer Cell, 2019
Ignaty Leshchiner, Shanye Yin, Thomas Kipps +2 more
exaly

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

Blood, 2011
Mario Cazzola, Luca Malcovati, Anna Galli' +2 more
exaly

SF3B1 AND MDS-RS: THE BIOLOGICAL PERSPECTIVE

Leukemia Research, 2023
openaire +1 more source

Prognostic value and clinical feature of SF3B1 mutations in myelodysplastic syndromes: A meta-analysis

Critical Reviews in Oncology/Hematology, 2019
Jiaqian Qi, Yue Han, Miao Miao
exaly

Pan-cancer analysis identifies mutations in SUGP1 that recapitulate mutant SF3B1 splicing dysregulation

Proceedings of the National Academy of Sciences of the United States of America, 2020
, Raúl Rabadan, Tomin Perea-Chamblee
exaly