Maren E. Speck

Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant‐negative, or hypomorphic alleles

Christina Matheny, Maren E. Speck, Patrick R. Cushing et al. · The EMBO Journal · 2007 · 114 citations · Full text

T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFβ dosage.

Laleh Talebian, Zhe Li, Yalin Guo et al. · Blood · 2006 · 70 citations · Full text

Runx1 dose-dependently regulates endochondral ossification during skeletal development and fracture healing

Do Y. Soung, Laleh Talebian, Christina Matheny et al. · Journal of Bone and Mineral Research · 2012 · 65 citations · Full text