Institut für Neuropathologie
Präsidium der Justus-Liebig-Universität Gießen » Fachbereiche » Fachbereich 11 - Humanmedizin » Dekanat Fachbereich 11 - Humanmedizin » Zentrum für Pathologie und Neuropathologie
Organisationstyp: Institut
Publikationen 
8 von 12 
8 von 12
- Dysregulated autophagy in restrictive cardiomyopathy due to Pro209Leu mutation in BAG3 (2018)
Schaenzer, A.; Rupp, S.; Graef, S.; et al. - Endothelial Dab1 signaling orchestrates neuro-glia-vessel communication in the central nervous system (2018)
Segarra, Marta; Aburto, Maria R.; Cop, Florian; et al. - Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model (2018)
Haslinger, Denise; Waltes, Regina; Yousaf, Afsheen; et al. - MIRACUM: Medical Informatics in Research and Care in University Medicine A Large Data Sharing Network to Enhance Translational Research and Medical Care (2018)
Prokosch, Hans-Ulrich; Acker, Till; Bernarding, Johannes; et al. - Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype-phenotype spectrum (2018)
Krenn, Martin; Salzer, Elisabeth; Simonitsch-Klupp, Ingrid; et al. - PHD3 Controls Lung Cancer Metastasis and Resistance to EGFR Inhibitors through TGFα (2018)
Dopeso, Higinio; Jiao, Hui-Ke; Cuesta, Angel M.; et al. - An Improved Anatomical MRI Technique With Suppression of Fixative Fluid Artifacts for the Investigation of Human Postmortem Brain Phantoms (2017)
Droby, Amgad; Yuen, Kenneth Sung Lai; Schaenzer, Anne; et al. - Hypoxia-inducible factor-1α activation in HPV-positive head and neck squamous cell carcinoma cell lines (2017)
Knuth, Jennifer; Sharma, Shachi J.; Wuerdemann, Nora; et al. - Integrating clinical decision support systems for pharmacogenomic testing into clinical routine - a scoping review of designs of user-system interactions in recent system development (2017)
Hinderer, Marc; Boeker, Martin; Wagner, Sebastian A.; et al. - Letter to the Editors: Concerning "Divergent clinical outcomes of alpha-glucosidase enzyme replacement therapy in two siblings with infantile-onset Pompe disease treated in the symptomatic or pre-symptomatic state" by Takashi et al. and Letter to the Editors by Ortolano et al. (2017)
Schaenzer, Anne; Giese, Kerstin; Viergutz, Lara; et al.
