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Institute of Human Genetics
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(729)
Research Grants
(48)
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Journal article
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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
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