Ludwig-Maximilians-Universität (LMU)

A miRNA181a/NFAT5 axis links impaired T cell tolerance induction with autoimmune type 1 diabetes (2018) Serr I, Scherm MG, Zahm AM, Schug J, Flynn VK, Hippich M, Kaelin S, et al. Journal article Combined effects of PLK1 and RAS in hepatocellular carcinoma reveal rigosertib as promising novel therapeutic "dual-hit" option (2018) Dietrich P, Freese K, Mahli A, Thasler WE, Hellerbrand C, Boßerhoff AK Journal article Dual-targeting triplebody 33-16-123 (SPM-2) mediates effective redirected lysis of primary blasts from patients with a broad range of AML subtypes in combination with natural killer cells (2018) Braciak TA, Roskopf CC, Wildenhain S, Fenn NC, Schiller CB, Schubert IA, Jacob U, et al. Journal article DNA methylation-based reclassification of olfactory neuroblastoma (2018) Capper D, Engel NW, Stichel D, Lechner M, Gloess S, Schmid S, Koelsche C, et al. Journal article Induction of sustained remission in early inflammatory arthritis with the combination of infliximab plus methotrexate: the DINORA trial (2018) Stamm TA, Machold KP, Aletaha D, Alasti F, Lipsky P, Pisetsky D, Landewe R, 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 Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease (2018) Jing J, Ekici AB, Sitter T, Schaeffnert E, Li Y, Kronenberg F, Koettgen A, et al. Journal article Identification of nine new susceptibility loci for endometrial cancer (2018) O'Mara TA, Glubb DM, Amant F, Annibali D, Ashton K, Attia J, Auer PL, et al. Journal article Epilepsy as a Network Disorder (2): What can we learn from other network disorders such as dementia and schizophrenia, and what are the implications for translational research? (2018) Scharfman HE, Kanner AM, Friedman A, Blümcke I, Crocker CE, Cendes F, Diaz-Arrastia R, et al. Journal article Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1 (2018) Eichinger A, Ponsel S, Bergmann C, Guenthner R, Hoefele J, Amann KU, Lange-Sperandio B Journal article