Radboud University Nijmegen

De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation (2018) Basilicata MF, Bruel AL, Semplicio G, Valsecchi CIK, Aktas T, Duffourd Y, Rumpf T, et al. Journal article The involvement of Toll-like receptor 9 in the pathogenesis of erosive autoimmune arthritis (2018) Fischer A, Abdollahi-Roodsaz S, Boehm C, Niederreiter B, Meyer B, Yau ACY, Lonnblom E, et al. Journal article Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation (2018) Teumer A, Chaker L, Groeneweg S, Li Y, Di Munno C, Barbieri C, Schultheiss UT, et al. Journal article Autoantibodies Recognizing Secondary NEcrotic Cells Promote Neutrophilic Phagocytosis and Identify Patients With Systemic Lupus Erythematosus (2018) Biermann M, Boeltz S, Pieterse E, Knopf J, Rech J, Bilyy R, Van Der Vlag J, et al. Journal article Diagnosis, monitoring and prevention of exposure-related non-communicable diseases in the living and working environment: DiMoPEx-project is designed to determine the impacts of environmental exposure on human health (2018) Budnik LT, Adam B, Albin M, Banelli B, Baur X, Belpoggi F, Bolognesi C, et al. Journal article Functional analyses of Pericentrin and Syne-2 interaction in ciliogenesis (2018) Falk N, Keßler K, Schramm SF, Boldt K, Becirovic E, Michalakis S, Regus-Leidig H, et al. Journal article Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility (2018) Earp M, Tyrer JP, Winham SJ, Lin HY, Chornokur G, Dennis J, Aben KKH, et al. Journal article International validation of the consensus Immunoscore for the classification of colon cancer: a prognostic and accuracy study (2018) Pages F, Mlecnik B, Marliot F, Bindea G, Ou FS, Bifulco C, Lugli A, et al. Journal article Sorafenib promotes graft-versus-leukemia activity in mice and humans through IL-15 production in FLT3-ITD-mutant leukemia cells (2018) Mathew NR, Baumgartner F, Braun L, O'Sullivan D, Thomas S, Waterhouse M, Mueller TA, et al. Journal article Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT). (2018) Neirijnck Y, Reginensi A, Renkema KY, Massa F, Kozlov VM, Dhib H, Bongers EMHF, et al. Journal article, Original article