Results 161 to 170 of about 10,998 (173)
Some of the next articles are maybe not open access.

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
Zhaoqi Liu   +2 more
exaly  

Pathologic Spectrum and Molecular Landscape of Myeloid Disorders Harboring SF3B1 Mutations

American Journal of Clinical Pathology, 2021
Dong Chen   +2 more
exaly  

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

The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial

Blood, 2013
David Gonzalez De Castro   +2 more
exaly  

Home - About - Disclaimer - Privacy