Baens M et al. MALT1 auto-proteolysis is essential for NF-κB-dependent gene transcription in activated lymphocytes. PLoS One. 2014 Aug 8;9(8):e103774.

Crauwels S. et al, Assessing Genetic Diversity among Brettanomyces Yeasts by DNA Fingerprinting and Whole-Genome Sequencing. Appl Environ Microbiol  80, 4398-4413,2014

De Vree P.J. et al, Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping. Nat Biotechnol 32, 1019-1025,2014.

Desmet SJ et al., Cofactor profiling of the glucocorticoid receptor from a cellular environment. Methods Mol Biol. 2014

Duitama Castellanos J. et al, Large-scale analysis of tandem repeat variability in the human genome. Nucleic Acids Res  42, 5728-5741,2014

Fernandes A.C. et al, Reduced synaptic vesicle protein degradation at lysosomes curbs TBC1D24/sky-induced neurodegeneration. J Cell Biol 207, 453-462,2014

Fendrych M. et al, Programmed Cell Death Controlled by ANAC033/SOMBRERO Determines Root Cap Organ Size in Arabidopsis. Curr Biol  24, 931-940,2014

Kalhorzadeh P. et al, Arabidopsis thaliana RNase H2 Deficiency Counteracts the Needs for the WEE1 Checkpoint Kinase but Triggers Genome Instability. Plant Cell 26, 3680-3692,2014

Kolmus K, et al., β-agonists selectively modulate proinflammatory gene expression in skeletal muscle cells via non-canonical nuclear crosstalk mechanisms. PLoS One. 2014 Mar 6;9(6):e90649. doi: 10.1371/journal.pone.0090649

Lin Y.C. et al, Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations. Nat Commun  5, 4767,2014

Pugach K. et al, Duplication of a promiscuous transcription factor drives the emergence of a new regulatory network. Nat Commun  5, 4868,2014

Van Damme P. et al, N-terminal proteomics and ribosome profiling provide a comprehensive view of the alternative translation initiation landscape in mice and men. Mol Cell Proteomics  13, 1245-1261,2014

Zhao H. et al, Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy. Eur J Hum Genet  22, 847-850,2014

Zhao H. et al, Mismatch repair deficiency endows tumors with a unique mutation signature and sensitivity to DNA double-strand breaks. eLIFE  e02725,2014