RUN (X) out of blood: emerging RUNX1 functions beyond hematopoiesis and links to Down syndrome

EJ Rozen, CD Ozeroff, MA Allen - Human Genomics, 2023 - Springer
Background RUNX1 is a transcription factor and a master regulator for the specification of
the hematopoietic lineage during embryogenesis and postnatal megakaryopoiesis …

Alternating high-fat diet enhances atherosclerosis by neutrophil reprogramming

JR Lavillegrand, R Al-Rifai, S Thietart, T Guyon… - Nature, 2024 - nature.com
Systemic immune responses caused by chronic hypercholesterolaemia contribute to
atherosclerosis initiation, progression and complications. However, individuals often change …

Epigenetic regulation of immune cells in systemic lupus erythematosus: insight from chromatin accessibility

ZX Gao, T He, P Zhang, X Hu, M Ge, YQ Xu… - Expert Opinion on …, 2024 - Taylor & Francis
ABSTRACT Introduction Systemic Lupus Erythematosus (SLE) is a multi-dimensional
autoimmune disease involving numerous tissues throughout the body. The chromatin …

Targeting the CD74 signaling axis suppresses inflammation and rescues defective hematopoiesis in RUNX1-familial platelet disorder

M Mohammadhosseini, T Enright, A Duvall… - Science Translational …, 2025 - science.org
Familial platelet disorder (FPD) is associated with germline RUNX1 mutations, establishing
a preleukemic state and increasing the risk of developing leukemia. Currently, there are no …

Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency

F Del Carpio-Cano, G Mao, LE Goldfinger… - Blood …, 2024 - ashpublications.org
Platelet α-granules have numerous proteins, some synthesized by megakaryocytes (MK)
and others not synthesized but incorporated by endocytosis, an incompletely understood …

[HTML][HTML] Dysregulated innate immune signaling cooperates with RUNX1 mutations to transform an MDS-like disease to AML

L Barreyro, AM Sampson, K Hueneman, K Choi… - Iscience, 2024 - cell.com
Dysregulated innate immune signaling is linked to preleukemic conditions and myeloid
malignancies. However, it is unknown whether sustained innate immune signaling …

Screening and identification of key biomarkers associated with endometriosis using bioinformatics and next-generation sequencing data analysis

B Vastrad, C Vastrad - Egyptian Journal of Medical Human Genetics, 2024 - Springer
Background Endometriosis is a common cause of endometrial-type mucosa outside the
uterine cavity with symptoms such as painful periods, chronic pelvic pain, pain with …

Functional and Practical Insights Into the Genetic Basis of Takayasu Arteritis

D Casares‐Marfil, AH Sawalha - ACR Open Rheumatology, 2025 - Wiley Online Library
Takayasu arteritis (TAK) is a rare vasculitis characterized by inflammation of large arteries.
Although the exact etiology of TAK remains unclear, a genetic predisposition to the disease …

[HTML][HTML] VHL synthetic lethality screens uncover CBF-β as a negative regulator of STING

JAC Bertlin, T Pauzaite, Q Liang, N Wit… - …, 2024 - pmc.ncbi.nlm.nih.gov
Clear cell renal cell carcinoma (ccRCC) represents the most common form of kidney cancer
and is typified by biallelic inactivation of the von Hippel-Lindau (VHL) tumour suppressor …

Targeting Heterochromatin Eliminates Malignant Hematopoietic Stem and Progenitor Cells in Chronic Myelomonocytic Leukemia Through Reactivation of …

D Hidaoui, R Chelbie, M Bohm, A Porquet, A Polyzou… - bioRxiv, 2024 - biorxiv.org
Chronic myelomonocytic leukemia (CMML) is a severe myeloid malignancy affecting the
elderly, for which therapeutic options are limited. DNA hypomethylating agents (HMAs) …