Institute of Human Genetics


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

IMPACT OF SINGLE NUCLEOTIDE POLYMORPHISMS RS1870377 A > T AND RS2305948 C > T ON ENDOTHELIAL CELL ACTIVATION UNDER NON-UNIFORM SHEAR STRESS (2017) Urschel K, Schacher N, Pasutto F, Achenbach S, Raaz-Schrauder D, Schrauder MG, Stumpfe F, Dietel B Conference contribution Inhibited Arginase-1 Expression by Fra-1 in Myeloid Cells Enhance Rheumatoid Arthritis Inflammation (2017) Hannemann N, Schnelzer A, Jordan J, Eberhardt M, Schleicher U, Uebe S, Ekici AB, et al. Conference contribution ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation (2017) Alber M, Kalscheuer VM, Marco E, Sherr E, Lesca G, Till M, Gradek G, et al. Journal article Impact of Superparamagnetic Iron Oxide Nanoparticles on Vocal Fold Fibroblasts: Cell Behavior and Cellular Iron Kinetics (2017) Poettler M, Fliedner A, Schreiber E, Janko C, Friedrich RP, Bohr C, Döllinger M, et al. Journal article The Trojan horse - neuroinflammatory impact of T cells in neurodegenerative diseases (2017) Sommer A, Winner B, Prots I Journal article PEDF Is Associated with the Termination of Chondrocyte Phenotype and Catabolism of Cartilage Tissue (2017) Klinger P, Lukassen S, Ferrazzi F, Ekici AB, Hotfiel T, Swoboda B, Aigner T, Gelse K Journal article Fra-2 regulates B cell development by enhancing IRF4 and Foxo1 transcription (2017) Ubieta K, Garcia M, Groetsch B, Uebe S, Stein M, Ekici AB, Schett G, et al. Journal article Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study (2017) Hein A, Rack B, Li L, Ekici AB, Reis A, Lux MP, Cunningham JM, et al. Journal article Genetic risk factors for ovarian cancer and their role for endometriosis risk (2017) Burghaus S, Fasching P, Haeberle L, Rübner M, Buechner K, Blum S, Engel A, et al. Journal article Haploinsufficiency of NR4A2 is associated with a neurodevelopmental phenotype with prominent language impairment (2017) Reuter M, Krumbiegel M, Schlueter G, Ekici AB, Reis A, Zweier C Journal article