recent & selected publications
see the complete list of publications
- Uzonyi, A., D. Dierks, R. Nir, O. S. Kwon, U. Toth, I. Barbosa, C. Burel, A. Brandis, W. Rossmanith, H. Le Hir, B. Slobodin, and S. Schwartz (2023). Exclusion of m6A from splice-site proximal regions by the exon junction complex dictates m6A topologies and mRNA stability. Mol. Cell 83, 237-51.
- Hochberg, I., L. A. M. Demain, J. Richer, K. Thompson, J. E. Urquhart, A. Rea, W. Pagarkar, A. Rodríguez-Palmero, A. Schlüter, E. Verdura, A. Pujol, P. Quijada-Fraile, A. Amberger, A. J. Deutschmann, S. Demetz, M. Gillespie, I. A. Belyantseva, H. J. McMillan, M. Barzik, G. M. Beaman, R. Motha, K. Y. Ng, J. O'Sullivan, S. G. Williams, S. S. Bhaskar, I. R. Lawrence, E. M. Jenkinson, J. L. Zambonin, Z. Blumenfeld, S. Yalonetsky, S. Oerum, W. Rossmanith, C. Genomics England Research, W. W. Yue, J. Zschocke, K. J. Munro, B. J. Battersby, T. B. Friedman, R. W. Taylor, R. T. O'Keefe, and W. G. Newman (2021). Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations. Am. J. Hum. Genet. 108, 2195-204.
- Schencking, I., W. Rossmanith, and R. K. Hartmann (2020). Diversity and evolution of RNase P. In: Evolutionary Biology—A Transdisciplinary Approach. P. Pontarotti, ed. (Springer, Switzerland). pp. 255-99.
- Summer, S., A. Smirnova, A. Gabriele, U. Toth, A. M. Fasemore, K. U. Förstner, L. Kuhn, J. Chicher, P. Hammann, G. Mitulović, N. Entelis, I. Tarassov, W. Rossmanith, and A. Smirnov (2020). YBEY is an essential biogenesis factor for mitochondrial ribosomes. Nucleic Acids Res. 48, 9762-86.
- Vilardo, E., F. Amman, U. Toth, A. Kotter, M. Helm, and W. Rossmanith (2020). Functional characterization of the human tRNA methyltransferases TRMT10A and TRMT10B. Nucleic Acids Res. 48, 6157-69.
- Garcia-Campos, M. A., S. Edelheit, U. Toth, M. Safra, R. Shachar, S. Viukov, R. Winkler, R. Nir, L. Lasman, A. Brandis, J. H. Hanna, W. Rossmanith, and S. Schwartz (2019). Deciphering the "m6A code" via antibody-independent quantitative profiling. Cell 178, 731-47.
- Brillante, N., M. Gößringer, D. Lindenhofer, U. Toth, W. Rossmanith, and R. K. Hartmann (2016).
Substrate recognition and cleavage-site selection by a single-subunit protein-only RNase P. Nucleic Acids Res. 44, 2323-36. - Weber, C., A. Hartig, R. K. Hartmann, and W. Rossmanith (2014).
Playing RNase P evolution: swapping the RNA catalyst for a protein reveals functional uniformity of highly divergent enzyme forms. PLoS Genet. 10, e1004506. - Vilardo, E., C. Nachbagauer, A. Buzet, A. Taschner, J. Holzmann, and W. Rossmanith (2012).
A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase–extensive moonlighting in mitochondrial tRNA biogenesis. Nucleic Acids Res. 40, 11583-93. - Holzmann, J., P. Frank, E. Löffler, K. L. Bennett, C. Gerner, and W. Rossmanith (2008).
RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme. Cell 135, 462-74.
see the complete list of publications
Copyright © Walter Rossmanith
legal notice/disclaimer
