T. Eggermann

Mutation analysis of multiple pilomatricomas in a patient with myotonic dystrophy type 1 suggests a DM1-associated hypermutation phenotype

This paper identifies somatic mutations in CTNNB1 in multiple pilomatricomas and a pilomatrical carcinoma from a DM1 patient, suggesting a tissue- and gene-specific hypermutation phenotype.

Interrupted reprogramming into induced pluripotent stem cells does not rejuvenate human mesenchymal stromal cells

This study shows that interrupting reprogramming of mesenchymal stromal cells into iPSCs does not rejuvenate the cells and may lead to chromosomal abnormalities.