T. Dietschy

The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability

I. Stagljar, R. Jiao, R. Freire, 2005, Journal of Cell Science.

The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress

I. Stagljar, I. Shevelev, T. Dietschy, 2007, Cellular and Molecular Life Sciences.

p300-mediated acetylation of the Rothmund-Thomson-syndrome gene product RECQL4 regulates its subcellular localization

Raymond H. Mak, I. Stagljar, D. Hess, 2009, Journal of Cell Science.

Summary p 300-mediated acetylation of the Rothmund-Thomson-syndrome gene product RECQL 4 regulates its subcellular localization

Raymond H. Mak, I. Stagljar, D. Hess, 2022 .

The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage

I. Stagljar, R. Jiao, V. Bohr, 2007, Oncogene.

The Bloom's syndrome helicase (BLM) interacts physically and functionally with p12, the smallest subunit of human DNA polymerase δ

J. Hoheisel, I. Stagljar, I. Hickson, 2008, Nucleic acids research.

p300-mediated acetylation of the Rothmund-Thomson-syndrome gene product RECQL4 regulates its subcellular localization

Raymond H. Mak, I. Stagljar, D. Hess, 2009, Journal of Cell Science.

Physical and functional interactions between Werner syndrome helicase and mismatch-repair initiation factors

Igor Stagljar, I. Stagljar, I. Shevelev, 2007, Nucleic acids research.