Schoenherr, Christopher J.

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

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ACVR1 R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A

Hatsell, S. J., Idone, V., Wolken, D. M. A., Huang, L., Kim, H. J., Wang, L., Wen, X., Nannuru, K. C., Jimenez, J., Xie, L., et al. (2015) · Science Translational Medicine

Heterotopic Ossification and Related ConditionsBone Tumor Diagnosis and Treatments

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CTCF maintains differential methylation at the Igf2/H19 locus

Schoenherr, C. J., Levorse, J. M., & Tilghman, S. M. (2003) · Nature Genetics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

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