Delphine G. Bernard
Brest, France
Last Updated: 09/26/2026
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Found 10 publications
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders.
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders.
Journal: Nature communications
Published: December 18, 2024
Vitamin B5 and succinyl-CoA improve ineffective erythropoiesis in SF3B1-mutated myelodysplasia.
Journal: Science translational medicine
Published: March 01, 2023
Cytogenetic and Genetic Abnormalities with Diagnostic Value in Myelodysplastic Syndromes (MDS): Focus on the Pre-Messenger RNA Splicing Process.
Journal: Diagnostics (Basel, Switzerland)
Published: May 30, 2022
Identification of altered cell signaling pathways using proteomic profiling in stable and progressive chronic lymphocytic leukemia.
Journal: Journal of leukocyte biology
Published: July 21, 2021
Splicing Anomalies in Myeloproliferative Neoplasms: Paving the Way for New Therapeutic Venues.
Journal: Cancers
Published: June 30, 2020
Human Cancer-Associated Mutations of SF3B1 Lead to a Splicing Modification of Its Own RNA.
Journal: Cancers
Published: February 11, 2020
Rare anemias due to genetic iron metabolism defects.
Journal: Mutation research. Reviews in mutation research
Published: December 06, 2017
Pre-mRNA splicing: when the spliceosome loses ground
Journal: Medecine sciences : M/S
Published: January 04, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026