Bernhard Payer

This study identifies the IFNγ pathway's role in accelerating iPSC reprogramming and X-chromosome reactivation through STAT3 signaling and TET-mediated demethylation.

This study investigates X-chromosome inactivation and reactivation dynamics in female mouse PGCLCs, showing that a precise temporal sequence is critical for meiotic potential.

The paper identifies a conserved gene expression signature linked to proliferation rate, showing it predicts growth rates across species and reveals lineage-specific differences in proliferation dynamics.

The paper shows that TAD formation on the inactive X occurs before transcription during X-reactivation, independent of transcriptional activity.

The paper studies alternative splicing dynamics during mouse B cell reprogramming into iPS cells and identifies three RNA-binding proteins involved in splicing regulation.

This study analyzes the transcriptomes of human oocytes at different maturation stages and finds that age affects specific gene pathways in matured oocytes.

This study identifies PRDM14 as a key factor for both global and X-chromosomal epigenetic reprogramming in migrating mouse primordial germ cells, showing its dosage-dependent role in H3K27me3 regulation.