Universität Bern

Die Mundarten der Walsertäler und des Tannbergs. (2013) Schallert O, Berchtold Schiestl S Authored book, Volume of book series ISL1 expression is not restricted to pancreatic well-differentiated neuroendocrine neoplasms, but is also commonly found in well and poorly differentiated neuroendocrine neoplasms of extrapancreatic origin (2013) Agaimy A, Erlenbach-Wünsch K, Konukiewitz B, Schmitt AM, Rieker R, Vieth M, Kiesewetter F, et al. Journal article The N. tabacum RIPA1 gene encodes for a novel pollen tube protein involved in Rac5 GTPase dependent control of polarized cell growth (2012) Stephan O, Cottier S, Fahlen S, Klahre U, Kost B Journal article Blockade of the hedgehog pathway inhibits osteophyte formation in arthritis. (2012) Ruiz-Heiland G, Horn A, Zerr P, Hofstetter W, Baum W, Stock M, Distler J, et al. Journal article Warum Pendeln nicht alle Probleme löst: Präferenzen für unterschiedliche Mobilitätsformen in "dual-career"-Partnerschaften (2012) Abraham M, Schönholzer T Journal article Diagnostic reproducibility of tumour budding in colorectal cancer: A multicentre, multinational study using virtual microscopy (2012) Puppa G, Senore C, Sheahan K, Vieth M, Lugli A, Zlobec I, Pecori S, et al. Journal article, Review article The inotropic peptide βARKct improves βAR responsiveness in normal and failing cardiomyocytes through G(βγ)-mediated L-type calcium current disinhibition. (2011) Völkers M, Weidenhammer C, Herzog N, Qiu G, Spaich K, von Wegner F, Peppel K, et al. Journal article, Original article Systemic antibody responses to gut commensal bacteria during chronic HIV-1 infection (2011) Haas A, Zimmermann K, Graw F, Slack E, Rusert P, Ledergerber B, Bossart W, et al. Journal article On the terminal homologation of physiologically active peptides as a means of increasing stability in human serum - Neurotensin, opiorphin, B27-KK10 epitope, NPY (2011) Seebach D, Lukaszuk A, Patora-Komisarska K, Podwysocka D, Gardiner J, Ebert MO, Reubi JC, et al. Journal article, Original article Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6) (2011) Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, Sticht H, et al. Journal article