RUNX1 Familial Platelet Disorder Latest Advances
Find the Latest Research About RUNX1 Familial Platelet Disorder
Last Updated: 04/28/2026
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Found 1029 publications
Acute degron-mediated RUNX1 loss reprograms enhancer activity to epigenetically drive epithelial destabilization and initiate cancer hallmarks.
Journal: bioRxiv : the preprint server for biology
Published: April 03, 2026
A genetic architect of opioid responses: Microglial Runx1.
Journal: Neuron
Published: December 31, 2025
Targeting RUNX1 Germline Variants: Agents Under Investigation.
Journal: Current hematologic malignancy reports
Published: October 21, 2025
RUNX1 promotes pathological retinal angiogenesis through von Willebrand factor.
Journal: Advances in ophthalmology practice and research
Published: September 29, 2025
P300 Promotes RUNX1 Transcription to Regulate Autophagy and Drive Corneal Neovascularization.
Journal: Investigative ophthalmology & visual science
Published: August 27, 2025
Macrophage-derived exosomes carrying miR-30a-5p alleviates IL-13/IL4-induced epithelial-mesenchymal transition in mouse bronchial epithelial cells via Runx1.
Journal: BMC pulmonary medicine
Published: August 26, 2025
Human Decidual RUNX1 Promotes Angiogenesis and Trophoblast Differentiation by Regulating Extracellular Vesicle Signaling.
Journal: bioRxiv : the preprint server for biology
Published: August 12, 2025
Targeting RUNX1 in Macrophages Facilitates Cardiac Recovery.
Journal: bioRxiv : the preprint server for biology
Published: August 08, 2025
GATA3 regulates Th1/Th2 balance in allergic rhinitis by interacting with RUNX1.
Journal: Future science OA
Published: August 01, 2025
RUNX1 N6-methyladenosine methylation enhances cytoskeleton remodelling and boosts cardiac fibrosis.
Journal: Cardiovascular research
Published: July 14, 2025
Last Updated: 04/28/2026