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Der Artikel untersucht Wahrnehmungsformen des Kapitalismus bei ex-sowjetischen Migranten nach ihrer Auswanderung nach Deutschland. Dabei konzentriere ich mich auf ihre Erfahrungen mit materiellen Gütern im allgemeinen und mit Konsum von Nahrung im besonderen. In der vorliegenden ethnographischen Studie stütze ich mich auf Interviews und teilnehmende Beobachtung, die ich zwischen 2002 und 2004 mit 45-60jährigen Migranten durchgeführt haben, die im Zeitraum zwischen 1990 - 1995 ausgewandert sind. Alle Befragten kommen aus zwei der europäischen Republiken der ehemaligen SU: Russland und Ukraine. Es handelt sich bei ihnen um eine Gruppe hochqualifizierter jüdischer Migranten.2 Da sie allerdings nicht religiös gebunden sind, spielt ihre Zugehörigkeit zum Judentum eine viel geringere Rolle als ihre sowjetische Erfahrung und ihre Zugehörigkeit zu den gebildeten Schichten der sowjetischen Intelligenz. Wahrscheinlich gilt das hier beobachtete Phänomen ganz allgemein für die ex-sowjetischen Migrantengruppen. ...
Background Drug resistance to chemotherapy is often associated with increased malignancy in neuroblastoma (NB). One explanation for the link between resistance and malignancy might be that resistance facilitates cancer progression and invasion. To investigate this hypothesis, adhesion, transendothelial penetration and NCAM (CD56) adhesion receptor expression of drug-resistant versus drug-sensitive NB tumor cells were evaluated. Methods Acquired drug resistance was mimicked by exposing parental UKF-NB-2, UKF-NB-3 or IMR-32 tumor cells to increasing concentrations of vincristine- (VCR) or doxorubicin (DOX) to establish the resistant tumor cell sublines UKF-NB-2VCR, UKF-NB-2DOX, UKF-NB-3VCR, UKF-NB-3DOX, IMR-32VCR and IMR-32DOX. Additionally, the malignant behaviour of UKF-NB-4, which already possessed the intrinsic multidrug resistance (MDR) phenotype, was analyzed. UKF-NB-4 exposed to VCR or DOX were designated UKF-NB-4VCR or UKF-NB-4DOX. Combined phase contrast - reflection interference contrast microscopy was used to separately evaluate NB cell adhesion and penetration. NCAM was analyzed by flow cytometry, western blot and RT-PCR. Results VCR and DOX resistant tumor sublines showed enhanced adhesion and penetration capacity, compared to their drug naive controls. Strongest effects were seen with UKF-NB-2VCR, UKF-NB-3VCR and IMR-32DOX. DOX or VCR treatment also evoked increased invasive behaviour of UKF-NB-4. The process of accelerated tumor invasion was accompanied by decreased NCAM surface and protein expression, and down-regulation of NCAM coding mRNA. Transfection of UKF-NB-4VCR cells with NCAM cDNA led to a significant receptor up-regulation, paralleled by diminished adhesion to an endothelial cell monolayer. Conclusions It is concluded that NB cells resistant to anticancer drugs acquire increased invasive capacity relative to non-resistant parental cells, and that enhanced invasion is caused by strong down-regulation of NCAM adhesion receptors.
Oral presentations Background: We selected peptide ligands for the HIV-1 packaging signal PSI by screening phage displayed peptide libraries. Peptide ligands were optimized by screening spot synthesis peptide membranes. The aim of this study is the functional characterization of these peptide ligands with respect to inhibition of HIV-1 replication. Methods: Phage displayed peptide libraries were screened with PSI-RNA structures. The Trp-rich peptide motifs were optimized for specific binding on spot synthesis peptide membranes. The best binding peptide was expressed intracellularly in fusion with RFP or linked to a protein transduction domain (PTD) for intracellular delivery. The effects on virion production were analyzed using pseudotyped lentiviral particles. Results: After positive and negative selection rounds, phages binding specifically to PSI-RNA were identified by ELISA. Peptide inserts contained conserved motifs of aromatic amino acids known to be implicated in binding of PSI-RNA by the natural Gag ligand. The filter assay identified HKWPWW as the best binding ligand for PSI-RNA, which is delivered into several cell lines by addition of a PTD. Compared to a control peptide, the HKWPWW peptide inhibited HIV-1 replication as deduced from reduced titers of culture supernatants. As HKWPWW also binds to the TAR-RNA like the natural nucleocapsid PSI-RNA ligand, the effect on Tat-TAR inhibition will also be analyzed. Currently T-cell lines are established which stably express HKWPWW as well as a control peptide, which will be infected with HIV-1 to monitor the ability of HKWPWW to inhibit wild type HIV-1 replication. Conclusion: The selection of a peptide ligand for PSI-RNA able to inhibit HIV-1 replication proves the suitability of the phage display technology for the selection of peptides binding to RNA-structures. This enables the indentification of peptides serving as leads to interfere with additional targets in the HIV-1 replication cycle.
Background Anti-angiogenic treatment is believed to have at least cystostatic effects in highly vascularized tumours like pancreatic cancer. In this study, the treatment effects of the angiogenesis inhibitor Cilengitide and gemcitabine were compared with gemcitabine alone in patients with advanced unresectable pancreatic cancer. Methods A multi-national, open-label, controlled, randomized, parallel-group, phase II pilot study was conducted in 20 centers in 7 countries. Cilengitide was administered at 600 mg/m2 twice weekly for 4 weeks per cycle and gemcitabine at 1000 mg/m2 for 3 weeks followed by a week of rest per cycle. The planned treatment period was 6 four-week cycles. The primary endpoint of the study was overall survival and the secondary endpoints were progression-free survival (PFS), response rate, quality of life (QoL), effects on biological markers of disease (CA 19.9) and angiogenesis (vascular endothelial growth factor and basic fibroblast growth factor), and safety. An ancillary study investigated the pharmacokinetics of both drugs in a subset of patients. Results Eighty-nine patients were randomized. The median overall survival was 6.7 months for Cilengitide and gemcitabine and 7.7 months for gemcitabine alone. The median PFS times were 3.6 months and 3.8 months, respectively. The overall response rates were 17% and 14%, and the tumor growth control rates were 54% and 56%, respectively. Changes in the levels of CA 19.9 went in line with the clinical course of the disease, but no apparent relationships were seen with the biological markers of angiogenesis. QoL and safety evaluations were comparable between treatment groups. Pharmacokinetic studies showed no influence of gemcitabine on the pharmacokinetic parameters of Cilengitide and vice versa. Conclusion There were no clinically important differences observed regarding efficacy, safety and QoL between the groups. The observations lay in the range of other clinical studies in this setting. The combination regimen was well tolerated with no adverse effects on the safety, tolerability and pharmacokinetics of either agent.
Die vorliegende Arbeit enthält ein Verzeichniss jener Crocodil-Schildkröten- und Eidechsen-Arten, welche bis zur Gegenwart als Bewohner Deutsch-Ost-Afrikas erkannt worden sind. Unter ihnen wurden dabei diejenigen, welche erst nach dem Erscheinen meines Buches: "Die Kriechthiere Deutsch-Ost-Afrikas", Berlin 1897, daselbst entdeckt wurden, durch Bezeichnung mit einem Stern (*) besonders hervorgehoben. Ferner enthält die Liste auch die Fundorte aller Exemplare dieser Arten, die seit dem Erscheinen jenes Buches bis zum August 1900 ins Museum für Naturkunde zu Berlin eingeliefert wurden, und daneben noch die Fundorte von Objecten, die dem Naturwissenschaftlichen Verein des Reg.-Bez. Frankfurt a. 0. angehören, von mir aber bestimmt worden sind. Um diese Thiere kenntlich zu machen, führe ich sie unter dem Zeichen F0 an. Nach Zusammenstellung dieser Liste ergab sich daraus, dass nunmehr aus Deutsch-Ost-Afrika 1 Crocodil, 7 Schildkrötenarten mit 1 Varietät und 65 Eidechsenarten mit etwa 14 Varietäten sicher nachgewiesen worden sind. ...