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Lehrstuhl für Humangenetik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Human Genetics
Overview
Publications
(514)
Research Grants
(37)
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Journal article
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The interaction of ENL with PAF1 mitigates polycomb silencing and facilitates murine leukemogenesis (2018)
Hetzner K, Garcia-Cuellar MP, Büttner C, Slany R
Journal article
Successful treatment with interleukin-17A antagonists of generalized pustular psoriasis in patients without IL36RN mutations (2018)
Wilsmann-Theis D, Schnell LM, Ralser-Isselstein V, Bieber T, Schoen MP, Hüffmeier U, Moessner R
Journal article
SWI/SNF protein expression status in fumarate hydratase-deficient renal cell carcinoma: immunohistochemical analysis of 32 tumors from 28 patients (2018)
Agaimy A, Amin MB, Gill A, Popp B, Reis A, Berney DM, Magi-Galluzzi C, et al.
Journal article
Risk, Prediction and Prevention of Hereditary Breast Cancer - Large-Scale Genomic Studies in Times of Big and Smart Data (2018)
Wunderle M, Olmes G, Nabieva N, Häberle L, Jud S, Hein A, Rauh C, et al.
Journal article
Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability (2018)
Scheller U, Pfisterer K, Uebe S, Ekici AB, Reis A, Jamra R, Ferrazzi F
Journal article
Characterization of germ cell differentiation in the male mouse through single-cell RNA sequencing (2018)
Lukassen S, Bosch E, Ekici AB, Winterpacht A
Journal article
Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutations (2018)
Wenzel A, Altmueller J, Ekici AB, Popp B, Stueber K, Thiele H, Pannes A, et al.
Journal article
Analysis of the expression pattern of the schizophrenia-risk and intellectual disability gene TCF4 in the developing and adult brain suggests a role in development and plasticity of cortical and hippocampal neurons (2018)
Jung M, Häberle B, Tschaikowsky T, Wittmann MT, Balta EA, Stadler VC, Zweier C, et al.
Journal article
Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017)
Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al.
Journal article
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
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