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Dr. rer. nat. Arif Bülent Ekici
List of publications:
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Institute of Human Genetics
Project Memberships
(7)
Publications
(285)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Activation of Epithelial Signal Transducer and Activator of Transcription 1 by Interleukin 28 Controls Mucosal Healing in Mice With Colitis and Is Increased in Mucosa of Patients With Inflammatory Bowel Disease. (2017)
Chiriac MT, Buchen B, Wandersee A, Hundorfean G, Günther C, Bourjau Y, Doyle SE, et al.
Journal article
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
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
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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