2024年12月25日 · RUNX1 (RUNX Family Transcription Factor 1) is a Protein Coding gene. Diseases associated with RUNX1 include Platelet Disorder, Familial, With Associated Myeloid …

2017年4月13日 · RUNX1 is a member of the core-binding factor family of transcription factors and is indispensable for the establishment of definitive hematopoiesis in vertebrates. RUNX1 is …

2021年3月4日 · RUNX1 -FPDMM is characterized by thrombocytopenia with normal platelet size; bleeding is often greater than expected due to qualitative platelet dysfunction. Myeloid …

The RUNX1 gene provides instructions for making a protein called runt-related transcription factor 1 (RUNX1). Like other transcription factors, the RUNX1 protein attaches (binds) to specific …

2025年2月8日 · RUNX1 predicts poor prognosis and correlates with tumor progression in clear cell renal carcinoma. RUNX1 promotes proliferation and migration in non-small cell lung …

RUNX1/RUNX1T1 is the most common fusion gene found in acute myeloid leukemia. Seminal contributions by many different research groups have revealed a complex regulatory network …

2022年10月28日 · Our results notably showed that Runx1 is a central regulator of articular cartilage homeostasis by orchestrating the YAP, TGFβ, and Wnt signaling pathways in the …

Runt-related transcription factor 1 (RUNX1) is frequently involved in the progression of acute leukemia. However, emerging and discoverable RUNX1 somatic mutations, RUNX1 …

RUNX1 Familial Platelet Disorder (RUNX1-FPD) is a rare condition that can affect many parts of the body and results in higher risk for developing certain cancers. This condition is caused by …

RUNX1 controls expression of genes essential for proper development in many cell lineages and tissues including blood, bone, cartilage, hair follicles and mammary glands. Compromised …