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References from New views on VUSs in RUNX1-FPD. Local targets link to admitted publications; unresolved targets remain external evidence.
10.1182/bloodadvances.2026019984 · 2026 · Admitted local publication
Secondary leukemia in patients with germline transcription factor mutations (RUNX1, GATA2, CEBPA)
10.1182/blood.2019000937 · 2020 · External reference
Familial mutations of the transcription factor RUNX1 (AML1, CBFA2) predispose to acute myeloid leukemia
10.1080/1042819031000139611 · 2004 · External reference
Familial myelodysplastic syndrome/acute leukemia syndromes: a review and utility for translational investigations
10.1111/nyas.12346 · 2014 · External reference
Hematologic malignancies in pediatric patients with RUNX1-familial platelet disorder with associated myeloid malignancy
10.1182/bloodadvances.2025017808 · 2026 · External reference
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
10.1038/s41375-021-01200-w · 2021 · External reference
Validation and clinical application of transactivation assays for RUNX1 variant classification
10.1182/bloodadvances.2021006161 · 2022 · External reference
Intrinsic transcriptional activation-inhibition domains of the polyomavirus enhancer binding protein 2/core binding factor alpha subunit revealed in the presence of the beta subunit
10.1128/mcb.18.5.2444 · 1998 · External reference
Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors
10.1073/pnas.95.20.11590 · 1998 · External reference
Identification and molecular characterization of a novel 3′ mutation in RUNX1 in a family with familial platelet disorder
10.3109/10428194.2010.503821 · 2010 · External reference