Institut für Biochemie


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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Unpublished / Preprint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

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Abstract

Journal

Variation of different histone deacetylases and the functional effects of HDAC inhibitors in hepatocellular carcinoma (2019) Freese K, Dietrich P, Boßerhoff AK, Hellerbrand C Conference contribution The Cortical Neuroimmune Regulator TANK Affects Emotional Processing and Enhances Alcohol Drinking: A Translational Study (2019) Müller CP, Chu C, Qin L, Liu C, Xu B, Gao H, Ruggeri B, et al. Journal article Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot (2019) Reuter MS, Jobling R, Chaturvedi RR, Manshaei R, Costain G, Heung T, Curtis M, et al. Journal article Profiling of gallbladder carcinoma reveals distinct miRNA profiles and activation of STAT1 by the tumor suppressive miRNA-145-5p (2019) Goeppert B, Truckenmueller F, Ori A, Fritz V, Albrecht T, Fraas A, Scherer D, et al. Journal article Inhibition of monoacylglycerol lipase for the treatment of liver disease: tempting but still playing with fire (2019) Hellerbrand C Journal article, Editorial The delta subunit of rod-specific photoreceptor cgmp phosphodiesterase (Pde6d) contributes to hepatocellular carcinoma progression (2019) Dietrich P, Hellerbrand C, Boßerhoff AK Journal article Post-transcriptional regulation of Argonaute2 in malignant melanoma (2019) Linck-Paulus L, Voeller D, Meister G, Boßerhoff AK Conference contribution Neuroblastoma RAS Viral Oncogene Homolog (NRAS) Is a Novel Prognostic Marker and Contributes to Sorafenib Resistance in Hepatocellular Carcinoma (2019) Dietrich P, Gaza A, Wormser L, Fritz V, Hellerbrand C, Boßerhoff AK Journal article The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study (2019) Papuc SM, Abela L, Steindl K, Begemann A, Simmons TL, Schmitt B, Zweier M, et al. Journal article Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes (2019) Begemann A, Acuna MA, Zweier M, Vincent M, Steindl K, Bachmann-Gagescu R, Hackenberg A, et al. Journal article