Refine
Year of publication
Document Type
- Article (15140)
- Part of Periodical (2805)
- Working Paper (2336)
- Doctoral Thesis (2001)
- Book (1737)
- Preprint (1705)
- Part of a Book (1055)
- Conference Proceeding (733)
- Report (471)
- Review (165)
Language
- English (28337) (remove)
Keywords
- taxonomy (715)
- new species (429)
- morphology (169)
- Deutschland (141)
- Syntax (125)
- Englisch (120)
- distribution (111)
- Deutsch (98)
- biodiversity (96)
- inflammation (94)
Institute
- Medizin (5109)
- Physik (3417)
- Wirtschaftswissenschaften (1881)
- Frankfurt Institute for Advanced Studies (FIAS) (1548)
- Biowissenschaften (1472)
- Center for Financial Studies (CFS) (1472)
- Informatik (1364)
- Biochemie und Chemie (1054)
- Sustainable Architecture for Finance in Europe (SAFE) (1045)
- House of Finance (HoF) (699)
With the emergence of immunotherapies, the understanding of functional HLA class I antigen presentation to T cells is more relevant than ever. Current knowledge on antigen presentation is based on decades of research in a wide variety of cell types with varying antigen presentation machinery (APM) expression patterns, proteomes and HLA haplotypes. This diversity complicates the establishment of individual APM contributions to antigen generation, selection and presentation. Therefore, we generated a novel Panel of APM Knockout Cell lines (PAKC) from the same genetic origin. After CRISPR/Cas9 genome-editing of ten individual APM components in a human cell line, we derived clonal cell lines and confirmed their knockout status and phenotype. We then show how PAKC will accelerate research on the functional interplay between APM components and their role in antigen generation and presentation. This will lead to improved understanding of peptide-specific T cell responses in infection, cancer and autoimmunity.
A single model system for integrative studies on multiple facets of antigen presentation is lacking. PAKC is a novel panel of ten cell lines knocked out for individual components of the HLA class I antigen presentation pathway. PAKC will accelerate HLA-I research in the fields of oncology, infectiology, and autoimmunity.
Background: Minimally invasive coronary artery bypass grafting (MICS CABG) has been introduced to abstain from median sternotomy due to related comorbidities. The aim of this study is to report the long term results of three different MICS CABG strategies: Partial lower sternotomy (PLS), totally endoscopic coronary artery bypass grafting (TECAB) and anterolateral thoracotomy (ALT). Moreover we aimed to compare these surgical approaches in terms of quality of pain and pain intensity.
Methods: From 1997 to 2006, 126 patients underwent MICS CABG surgeries in our department through different surgical approaches: 43 PLS, 63 TECAB and 20 ALT. Preoperative characteristics were similar between groups. There were 90 males (71.4%) and 36 (28.6%) females with a mean age of 62±11 years (Range 36 to 90).
Results: There was no in-hospital mortality. Conversion to minithoracotomy was necessary in 2 (1.6%) patients and conversion to sternotomy was performed in 1 (0.8%) patient. Length of hospital stay was comparable in patients who underwent PLS or TECAB, but both groups had significantly shorter hospital stays than ALT patients (p<0.05). Two patients in group ALT developed temporary neurological complications postoperatively, which was significantly higher than that in groups TECAB (n=0) and PLS (n=0) (p<0.05). Mean follow-up was 12.2±2.1 (range 7.2 to 16.1) years with completed in 81.7 % of the patients. There were 17 late deaths. Freedom from graft problems was 87.5%, 86.5% and 94.7%; freedom from percutaneous coronary interventions (PCI) was 78.1%, 82.7% and 68.4% and freedom from Re-CABG was 100%, 96.1% and 94.7% in PLS, TECAB and ALT group, respectively. Pain intensity was similar between all three groups.
Conclusion: MICS CABG can be performed safely and effectively. Short and long-term outcomes of MICS CABG are comparable with those of the conventional CABG. There were no major differences regarding pain intensity between all three groups, although all three minimally invasive techniques have completely different surgical accesses.
One of the cruxes of Walter Benjamin’s work is the tension between an indebting and an expiating "memoria", i. e. the afflicting and the salvific insistence of history within the present moment. On the one hand, memory inscribes itself onto spaces and bodies in the violent and painful fashion of Kafka's "Penal Colony" apparatus. On the other hand, it can, in the form of rememoration ('Eingedenken'), sublate these very inscriptions. This sublation usually involves some form of redemptive, timely (re-)verbalization, but Benjamin’s conception of it varies. To gain a better insight into this inherent, varying tension, the article will take a closer look at the connection between pain, memory and law-positing violence in some Benjaminian texts, occasionally relating them to the historical background of his discussion.
Generic, subgeneric, specific, subspecific, and inlra-subspecific names in Paederus (sensu lato) are compiled alphabetically with literature references, showing that 622 specific names stand in the literature as valid. Five replacement names are required due to homonymy: Paederus cumanus Frank [nom. nou. for Paederus bicolor Wendeler nec Olivier], Paederus sulawesi Frank [nom. nov. for Paederus melanocephlus Heller nec Fabricius], Paederus zairensis Frank [nom. nov. for Paederus orophilus Fagel nec Paederidus brunnescens orophilus (Fagel)], Paederus irianensis Frank [nom. nou. for Paederus litoreus Last nec Paederus littoreus Austin], and Oreopaederus manyemensis Frank [nom. nm. for Oreopaederus ater (Bernhauer) nec Paederidus rubrothoracicus ater (Eichler)]. Four unjustified replacement names (Paederus archeus Blackwelder, Paederus homonymus Blackwelder, Paederus erichsoni Wollaston, and Paederus samoensis Fauvel) are here attributed to their respective senior synonyms (Paederus elongatus Wendeler, Paederus tricolor Erichson, Paederus angolensis Erichson, and Paederus vitiensis Fauvel).
The transcription factor Tal1 is a critical activator or repressor of gene expression in hematopoiesis and leukaemia. The mechanism by which Tal1 differentially influences transcription of distinct genes is not fully understood. Here we show that Tal1 interacts with the peptidylarginine deiminase IV (PADI4). We demonstrate that PADI4 can act as an epigenetic coactivator through influencing H3R2me2a. At the Tal1/PADI4 target gene IL6ST the repressive H3R2me2a mark triggered by PRMT6 is counteracted by PADI4, which augments the active H3K4me3 mark and thus increases IL6ST expression. In contrast, at the CTCF promoter PADI4 acts as a repressor. We propose that the influence of PADI4 on IL6ST transcription plays a role in the control of IL6ST expression during lineage differentiation of hematopoietic stem/progenitor cells. These results open the possibility to pharmacologically influence Tal1 in leukaemia.
We study online secretary problems with returns in combinatorial packing domains with n candidates that arrive sequentially over time in random order. The goal is to determine a feasible packing of candidates of maximum total value. In the first variant, each candidate arrives exactly twice. All 2n arrivals occur in random order. We propose a simple 0.5‐competitive algorithm. For the online bipartite matching problem, we obtain an algorithm with ratio at least 0.5721 − o(1), and an algorithm with ratio at least 0.5459 for all n ≥ 1. We extend all algorithms and ratios to k ≥ 2 arrivals per candidate. In the second variant, there is a pool of undecided candidates. In each round, a random candidate from the pool arrives. Upon arrival a candidate can be either decided (accept/reject) or postponed. We focus on minimizing the expected number of postponements when computing an optimal solution. An expected number of Θ(n log n) is always sufficient. For bipartite matching, we can show a tight bound of O(r log n), where r is the size of the optimum matching. For matroids, we can improve this further to a tight bound of O(r′ log(n/r′)), where r′ is the minimum rank of the matroid and the dual matroid.
By establishing the date of its first publication, Noserus Foerster, 1863 (Hymenoptera, Braconidae) is shown to be a junior primary homonym of Noserus LeConte, 1862 (Coleoptera, Zopheridae). The substitute name for Noserus Foerster is that of its subjective synonym, Pachystigmus Hellén, 1927 [type species: Pachystigmus nitidulus Hellén, 1927]. Other described species in the genus are: Pachystigmus facialis (Foerster, 1863) New Combination; P. similis (Szépligeti, 1896) New Combination, P. nitidulus Hellén, 1927, P. gigas (Tobias, 1964)New Combination, P. occipitalis (Belokobylskij, 1986) New Combination, P. olgensis (Belokobylskij, 1994) New Combination, and P. sculpturator (Belokobylskij, 1999) New Combination.
PaCATB : a secreted catalase protecting Podospora anserina against exogenous oxidative stress
(2011)
A differential mass spectrometry analysis of secreted proteins from juvenile and senescentPodospora anserina cultures revealed age-related differences in protein profiles. Among other proteins with decreased abundance in the secretome of senescent cultures a catalase, termed PaCATB, was identified. Genetic modulation of the abundance of PaCATB identified differential effects on the phenotype of the corresponding strains. Deletion of PaCatB resulted in decreased resistance, over-expression in increased resistance against hydrogen peroxide. While the lifespan of the genetically modified strains was found to be unaffected under standard growth conditions, increased exogenous hydrogen peroxide stress in the growth medium markedly reduced the lifespan of the PaCatB deletion strain but extended the lifespan of PaCatB over-expressors. Overall our data identify a component of the secretome of P. anserina as a new effective factor to cope with environmental stress, stress that under natural conditions is constantly applied on organisms and influences aging processes.
Nitric oxide (NO) represents a short-lived mediator that pivotally drives keratinocyte movements during cutaneous wound healing. In this study, we have identified p68 DEAD box RNA helicase (p68) from a NO-induced differential keratinocyte cDNA library. Subsequently, we have analyzed regulation of p68 by wound-associated mediators in the human keratinocyte cell line HaCaT. NO, serum, growth factors and pro-inflammatory cytokines were potent inducers of p68 expression in the cells. p68 was constitutively expressed in murine skin, but rapidly down-regulated upon injury. The down-regulation appeared to be transient, as p68 protein expression increased again after the inflammatory phase of repair. However, p68 protein expression did not completely disappear during wound inflammation, as immunohistochemistry and cell fractiona tion analysis revealed a restricted localization of p68 in keratinocyte nuclei of the developing epithelium. In line, cultured human (HaCaT) and murine (PAM 212) keratinocyte cell lines showed a nuclear localization of the helicase. Moreover, confocal microscopy revealed a strong localization of p68 protein within the nucleoli of the keratinocytes. Functional analyses demonstrated that p68 strongly participates in keratinocyte proliferation and gene expression. Keratinocytes that constitutively overexpressed p68 protein were characterized by a marked increase in serum-induced proliferation and vascular endothelial growth factor (VEGF) expression, whereas down-regulation of endogenous p68 using small interfering RNA (siRNA) markedly attenuated serum-induced proliferation and VEGF expression. Altogether, our results suggest a tightly controlled expression and nucleolar localization of p68 in keratinocytes in vitro and during skin repair in vivo that functionally contributes to keratinocyte proliferation and gene expression.