Lehrstuhl für Humangenetik


close-button

Types of publications

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Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Body mass index and breast cancer survival: a Mendelian randomization analysis (2017) Guo Q, Burgess S, Turman C, Bolla MK, Wang Q, Lush M, Abraham J, et al. Journal article Clinical validation of genetic variants associated with in vitro chemotherapy-related lymphoblastoid cell toxicity (2017) Fasching P, Häberle L, Rack B, Li L, Hein A, Ekici AB, Reis A, et al. Journal article Dual role of the mycobacterial cord factor TDM in cross-regulation of macrophage responses to IFN gamma (2017) Killy B, Huber A, Ekici AB, Wirtz S, Dalpke A, Lang R Conference contribution Alternative splicing and nonsense-mediated mRNA decay contribute to regulation of LOXL1 expression in response to cellular stress in pseudoexfoliation (2017) Berner D, Zenkel M, Pasutto F, Schoedel J, Reis A, Kruse F, Schlötzer-Schrehardt U Conference contribution 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 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