Bauer, Christian R. K. D.

[["dc.bibliographiccitation.firstpage","35"],["dc.bibliographiccitation.issue","1-2"],["dc.bibliographiccitation.journal","Veterinary Microbiology"],["dc.bibliographiccitation.lastpage","42"],["dc.bibliographiccitation.volume","160"],["dc.contributor.author","Schulz, Claudia"],["dc.contributor.author","Eschbaumer, Michael"],["dc.contributor.author","Ziller, Mario"],["dc.contributor.author","Waeckerlin, Regula"],["dc.contributor.author","Beer, Martin"],["dc.contributor.author","Gauly, Matthias"],["dc.contributor.author","Grevelding, Christoph G."],["dc.contributor.author","Hoffmann, Bernd"],["dc.contributor.author","Bauer, Christian R."],["dc.date.accessioned","2018-11-07T09:03:32Z"],["dc.date.available","2018-11-07T09:03:32Z"],["dc.date.issued","2012"],["dc.description.abstract","Bluetongue (BT) is a major disease of ruminant livestock that can have a substantial impact on income and animal welfare. In South American camelids (SAC), fatalities related to bluetongue virus (BTV) infection were reported in Germany and France during the recent BTV-8 and BTV-1 epizootics, which raised concern about the role of SAC in the epidemiology of BTV. Therefore, a large-scale serological and virological study was conducted in Germany from autumn 2008 to spring 2009. Risk factors associated with BTV infection were analysed by multiple logistic regression. These included age, species, gender and housing arrangements of SAC as well as the location of the herds and the presence of ruminants on farms.Altogether, 249 (14.3%) of 1742 SAC were found seropositive by BTV ELISA, and 43 (47.3%) of the 91 herds had at least one BTV-seropositive SAC. However, no BTV RNA was detected in any of the seropositive samples. Seroprevalence depended on the sampling region and probably on age, but not on any other analysed risk factors associated with BTV infection in ruminants. The highest seroprevalence was found in the west of Germany where the BTV-8 epizootic started in 2006. Recorded BTV-8 related disease and fatalities are discussed. Although the prevalence of BTV-8 antibodies was high in some regions, the virological results indicate that SAC play a negligible role in the epidemiology of this virus infection. (C) 2012 Elsevier B.V. All rights reserved."],["dc.identifier.doi","10.1016/j.vetmic.2012.05.028"],["dc.identifier.isi","000310418300006"],["dc.identifier.pmid","22704245"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/24915"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Bv"],["dc.relation.issn","0378-1135"],["dc.title","Cross-sectional study of bluetongue virus serotype 8 infection in South American camelids in Germany (2008/2009)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","272"],["dc.bibliographiccitation.issue","3-4"],["dc.bibliographiccitation.journal","Veterinary Parasitology"],["dc.bibliographiccitation.lastpage","281"],["dc.bibliographiccitation.volume","214"],["dc.contributor.author","Schulz, Claudia"],["dc.contributor.author","Ziller, Mario"],["dc.contributor.author","Kampen, Helge"],["dc.contributor.author","Gauly, Matthias"],["dc.contributor.author","Beer, Martin"],["dc.contributor.author","Grevelding, Christoph G."],["dc.contributor.author","Hoffmann, Bernd"],["dc.contributor.author","Bauer, Christian R."],["dc.contributor.author","Werner, Doreen"],["dc.date.accessioned","2018-11-07T09:47:29Z"],["dc.date.available","2018-11-07T09:47:29Z"],["dc.date.issued","2015"],["dc.description.abstract","Palearctic species of Culicoides (Diptera, Ceratopogonidae), in particular of the Obsoletus and Pulicaris complexes, were identified as putative vectors of bluetongue virus serotype 8 (BTV-8) on ruminant farms during the epizootic in Germany from 2006 to 2009. BTV may cause severe morbidity and mortality in ruminants and sporadically in South American camelids (SAC). However, the fauna of Culicoides spp. on SAC farms has not been investigated. Therefore, the ceratopogonid fauna was monitored on three farms with BTV-seropositive SAC in Germany. Black-light traps were set up on pastures and in stables from summer 2008 to autumn 2009. Additionally, ceratopogonids were caught in emergence traps mounted on llama dung and dung-free pasture from spring to autumn 2009. After morphological identification, selected Culicoides samples were analysed for BTV-RNA by real-time RT-PCR. The effects of the variables 'location', 'temperature' and 'humidity' on the number of Culicoides caught in black-light traps were modelled using multivariable Poisson regression. In total, 26 species of Culicoides and six other genera of biting midges were identified. The most abundant Culicoides spp. collected both outdoors and indoors with black-light traps belonged to the Obsoletus (77.4%) and Pulicaris (16.0%) complexes. The number of Culicoides peaked in summer, while no biting midges were caught during the winter months. Daily collections of Culicoides were mainly influenced by the location and depended on the interaction of temperature and humidity. In the emergence traps, species of the Obsoletus complex predominated the collections. In summary, the absence of BTV-RNA in any of the analysed Culicoides midges and in the BTV-seropositive SAC on the three farms together with the differences in the pathogenesis of BTV-8 in SAC compared to ruminants suggests a negligible role of SAC in the spread of the virus. Although SAC farms may provide similar suitable habitats for putative Culicoides vectors than ruminant farms, the results suggest that geographic and meteorological factors had a stronger influence on Culicoides abundance than the animal species. (C) 2015 Elsevier B.V. All rights reserved."],["dc.identifier.doi","10.1016/j.vetpar.2015.09.021"],["dc.identifier.isi","000367112600006"],["dc.identifier.pmid","26489592"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/35123"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Bv"],["dc.relation.issn","1873-2550"],["dc.relation.issn","0304-4017"],["dc.title","Culicoides vector species on three South American camelid farms seropositive for bluetongue virus serotype 8 in Germany 2008/2009"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","46"],["dc.bibliographiccitation.journal","Experimental Parasitology"],["dc.bibliographiccitation.lastpage","56"],["dc.bibliographiccitation.volume","163"],["dc.contributor.author","Gondim, Luis F. P."],["dc.contributor.author","Wolf, Alexander"],["dc.contributor.author","Vrhovec, M. Globokar"],["dc.contributor.author","Pantchev, Nikola"],["dc.contributor.author","Bauer, Christian R."],["dc.contributor.author","Langenmayer, Martin C."],["dc.contributor.author","Bohne, Wolfgang"],["dc.contributor.author","Teifke, Jens P."],["dc.contributor.author","Dubey, Jitender P."],["dc.contributor.author","Conraths, Franz J."],["dc.contributor.author","Schares, Gereon"],["dc.date.accessioned","2018-11-07T10:16:31Z"],["dc.date.available","2018-11-07T10:16:31Z"],["dc.date.issued","2016"],["dc.description.abstract","Toxoplasma gondii infects animals habiting terrestrial and aquatic environments. Its oocysts and tissue cysts are important for the horizontal transmission of this parasite. The oocyst and tissue cyst walls are crucial for the ability of the parasite to persist in the environment or in animal tissues, respectively. However, the composition of these walls is not well understood. We report the generation of monoclonal antibodies directed against wall components using mice immunized with oocyst antigens of T gondii. One monoclonal antibody (mAb) G1/19 reacted solely with T. gondii sporozoites. The respective antigen had a relative molecular weight (Mr) of 30 kDa. MAb G1/19 failed to react with sporozoites of any other coccidian parasite species tested (Hammondia hammondi, Hammondia heydorni, Cystoisospora felis, Eimeria bovis, Sarcocystis sp.). Another mAb, designated K8/15-15, recognized antigens in sporocyst walls of the parasite and in the walls of in vivo or in vitro produced tissue cysts, as demonstrated by immunofluorescence and immunoblot assays. Antigens of 80 to a high molecular weight protein of about 350 kDa Mr were recognized by this antibody using antigen extracts from sporocysts, and from in vitro or in vivo generated tissue cysts of the parasite. Tissue cyst and sporocyst walls of H. hammondi and H. heydorni, and tissue cysts of Neospora caninum were also recognized by mAb K8/15-15. Sporocyst walls of C. felis also reacted to this mAb. The cyst walls of Sarcocystis sp. and Besnoitia besnoiti were not recognized by mAb K8/15-15. Reactivity by a single mAb against T. gondii antigens in tissue cysts and sporocysts had not been reported previously. MAb K8/15-15 may be a practical tool for the identification of both cysts and sporocysts of the parasite, and may also be potentially employed in proteomic studies on the identification of new components of the cyst and sporocyst walls of T. gondii. (C) 2016 Elsevier Inc. All rights reserved."],["dc.identifier.doi","10.1016/j.exppara.2016.01.014"],["dc.identifier.isi","000372667700007"],["dc.identifier.pmid","26836446"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/41055"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Academic Press Inc Elsevier Science"],["dc.relation.issn","1090-2449"],["dc.relation.issn","0014-4894"],["dc.title","Characterization of an IgG monoclonal antibody targeted to both tissue cyst and sporocyst walls of Toxoplasma gondii"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.contributor.author","Knopp, Cornelius"],["dc.contributor.author","Bauer, Christian R. K. D."],["dc.contributor.author","Baum, Benjamin"],["dc.contributor.author","Löhnhardt, Benjamin"],["dc.contributor.author","Nietert, Manuel Manfred"],["dc.contributor.author","Beißbarth, Tim"],["dc.contributor.author","Sax, Ulrich"],["dc.date.accessioned","2020-03-27T11:22:14Z"],["dc.date.available","2020-03-27T11:22:14Z"],["dc.date.issued","2016"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/63384"],["dc.notes.preprint","yes"],["dc.relation.conference","Conference: HEC 2016 - Health-Exploring Complexity: An Interdisciplinairy Systems Approach"],["dc.relation.eventlocation","München"],["dc.relation.eventstart","2016-08"],["dc.relation.iserratumof","yes"],["dc.title","A validatable data management solution for multi-center research consortia: research data management with openBIS"],["dc.type","conference_paper"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","691"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Journal of Alzheimer s Disease"],["dc.bibliographiccitation.lastpage","705"],["dc.bibliographiccitation.volume","54"],["dc.contributor.author","Klafki, Hans-W."],["dc.contributor.author","Hafermann, Henning"],["dc.contributor.author","Bauer, Christian R."],["dc.contributor.author","Haussmann, Ute"],["dc.contributor.author","Kraus, Inga"],["dc.contributor.author","Schuchhardt, Johannes"],["dc.contributor.author","Muck, Stephan"],["dc.contributor.author","Scherbaum, Norbert"],["dc.contributor.author","Wiltfang, Jens"],["dc.date.accessioned","2018-11-07T10:19:59Z"],["dc.date.available","2018-11-07T10:19:59Z"],["dc.date.issued","2016"],["dc.description.abstract","Acomprehensive assay validation campaign of a commercially available chemiluminescence multiplex immunoassay for the simultaneous measurement of the amyloid-beta peptides A beta(38), A beta(40), and A beta(42) in human cerebrospinal fluid (CSF) is presented. The assay quality parameters we addressed included impact of sample dilution, parallelism, lower limits of detection, lower limits of quantification, intra- and inter-assay repeatability, analytical spike recoveries, and between laboratory reproducibility of the measurements. The assay performed well in our hands and fulfilled a number of predefined acceptance criteria. The CSF levels of A beta(40) and A beta(42) determined in a clinical cohort (n = 203) were statistically significantly correlated with available ELISA data of A beta(1-40) (n = 158) and A beta(1-42) (n = 179) from a different laboratory. However, Bland-Altman method comparison indicated systematic differences between the assays. The data presented here furthermore indicate that the CSF concentration of A beta(40) can surrogate total CSF A beta and support the hypothesis that the A beta(42)/A beta(40) ratio outperforms CSF A beta(42) alone as a biomarker for Alzheimer's disease due to a normalization to total A beta levels."],["dc.identifier.doi","10.3233/JAD-160398"],["dc.identifier.isi","000384087200023"],["dc.identifier.pmid","27567847"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/41786"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Ios Press"],["dc.relation.issn","1875-8908"],["dc.relation.issn","1387-2877"],["dc.title","Validation of a Commercial Chemiluminescence Immunoassay for the Simultaneous Measurement of Three Different Amyloid-beta Peptides in Human Cerebrospinal Fluid and Application to a Clinical Cohort"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","257"],["dc.bibliographiccitation.issue","3-4"],["dc.bibliographiccitation.journal","Veterinary Microbiology"],["dc.bibliographiccitation.lastpage","265"],["dc.bibliographiccitation.volume","154"],["dc.contributor.author","Schulz, Claudia"],["dc.contributor.author","Eschbaumer, Michael"],["dc.contributor.author","Rudolf, Miriam"],["dc.contributor.author","Koenig, Patricia"],["dc.contributor.author","Keller, Markus"],["dc.contributor.author","Bauer, Christian R."],["dc.contributor.author","Gauly, Matthias"],["dc.contributor.author","Grevelding, Christoph G."],["dc.contributor.author","Beer, Martin"],["dc.contributor.author","Hoffmann, Bernd"],["dc.date.accessioned","2018-11-07T09:14:15Z"],["dc.date.available","2018-11-07T09:14:15Z"],["dc.date.issued","2012"],["dc.description.abstract","Bluetongue (BT) is an infectious, non-contagious disease of wild and domestic ruminants. It is caused by bluetongue virus (BTV) and transmitted by Culicoides biting midges. Since 1998, BT has been emerging throughout Europe, threatening not only the naive ruminant population. Historically, South American camelids (SAC) were considered to be resistant to BT disease. However, recent fatalities related to BTV in captive SAC have raised questions about their role in BTV epidemiology. Data on the susceptibility of SAC to experimental infection with BTV serotype 8 (BTV-8) were collected in an animal experiment. Three alpacas (Vicugna pacos) and three llamas (Lama glama) were experimentally infected with BTV-8. They displayed very mild clinical signs. Seroconversion was first measured 6-8 days after infection (dpi) by ELISA, and neutralising antibodies appeared 10-13 dpi. BTV-8 RNA levels in blood were very low, and quickly cleared after seroconversion. However, spleens collected post-mortem were still positive for BTV RNA, over 71 days after the last detection in blood samples. Virus isolation was only possible from blood samples of two alpacas by inoculation of highly sensitive interferon alpha/beta receptor-deficient (IFNAR(-/-)) mice. An in vitro experiment demonstrated that significantly lower amounts of BTV-8 adsorb to SAC blood cells than to bovine blood cells. Although this experiment showed that SAC are generally susceptible to a BTV-8 infection, it indicates that these species play a negligible role in BTV epidemiology. (C) 2011 Elsevier B.V. All rights reserved."],["dc.identifier.doi","10.1016/j.vetmic.2011.07.025"],["dc.identifier.isi","000299582000006"],["dc.identifier.pmid","21862245"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/27366"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Bv"],["dc.relation.issn","1873-2542"],["dc.relation.issn","0378-1135"],["dc.title","Experimental infection of South American camelids with bluetongue virus serotype 8"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","479"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Briefings in Bioinformatics"],["dc.bibliographiccitation.lastpage","487"],["dc.bibliographiccitation.volume","18"],["dc.contributor.author","Bauer, Christian R."],["dc.contributor.author","Knecht, Carolin"],["dc.contributor.author","Fretter, Christoph"],["dc.contributor.author","Baum, Benjamin"],["dc.contributor.author","Jendrossek, Sandra"],["dc.contributor.author","Ruehlemann, Malte"],["dc.contributor.author","Heinsen, Femke-Anouska"],["dc.contributor.author","Umbach, Nadine"],["dc.contributor.author","Grimbacher, Bodo"],["dc.contributor.author","Franke, Andre"],["dc.contributor.author","Lieb, Wolfgang"],["dc.contributor.author","Krawczak, Michael"],["dc.contributor.author","Huett, Marc-Thorsten"],["dc.contributor.author","Sax, Ulrich"],["dc.date.accessioned","2018-11-07T10:24:26Z"],["dc.date.available","2018-11-07T10:24:26Z"],["dc.date.issued","2017"],["dc.description.abstract","Electronic access to multiple data types, from generic information on biological systems at different functional and cellular levels to high-throughputmolecular data from human patients, is a prerequisite of successful systems medicine research. However, scientists often encounter technical and conceptual difficulties that forestall the efficient and effective use of these resources. We summarize and discuss some of these obstacles, and suggest ways to avoid or evade them. The methodological gap between data capturing and data analysis is huge in human medical research. Primary data producers often do not fully apprehend the scientific value of their data, whereas data analysts maybe ignorant of the circumstances under which the data were collected. Therefore, the provision of easy-to-use data access tools not only helps to improve data quality on the part of the data producers but also is likely to foster an informed dialogue with the data analysts. We propose a means to integrate phenotypic data, questionnaire data and microbiome data with a user-friendly Systems Medicine toolbox embedded into i2b2/tranSMART. Our approach is exemplified by the integration of a basic outlier detection tool and a more advanced microbiome analysis (alpha diversity) script. Continuous discussion with clinicians, data managers, biostatisticians and systems medicine experts should serve to enrich even further the functionality of toolboxes like ours, being geared to be used by 'informed non-experts' but at the same time attuned to existing, more sophisticated analysis tools."],["dc.identifier.doi","10.1093/bib/bbw024"],["dc.identifier.isi","000400968000012"],["dc.identifier.pmid","27016392"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42664"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Oxford Univ Press"],["dc.relation.issn","1477-4054"],["dc.relation.issn","1467-5463"],["dc.title","Interdisciplinary approach towards a systems medicine toolbox using the example of inflammatory diseases"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","S6"],["dc.bibliographiccitation.issue","Suppl 1"],["dc.bibliographiccitation.journal","Journal of Clinical Bioinformatics"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Bauer, Christian"],["dc.contributor.author","Ganslandt, Thomas"],["dc.contributor.author","Baum, Benjamin"],["dc.contributor.author","Christoph, Jan"],["dc.contributor.author","Engel, Igor"],["dc.contributor.author","Löbe, Matthias"],["dc.contributor.author","Mate, Sebastian"],["dc.contributor.author","Prokosch, Hans-Ulrich"],["dc.contributor.author","Sax, Ulrich"],["dc.contributor.author","Stäubert, Sebastian"],["dc.contributor.author","Winter, Alfred"],["dc.date.accessioned","2016-03-17T17:03:59Z"],["dc.date.accessioned","2021-10-27T13:20:27Z"],["dc.date.available","2016-03-17T17:03:59Z"],["dc.date.available","2021-10-27T13:20:27Z"],["dc.date.issued","2015"],["dc.date.updated","2016-03-17T17:03:59Z"],["dc.identifier.doi","10.1186/2043-9113-5-S1-S6"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/13128"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91967"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.relation.orgunit","Universitätsmedizin Göttingen"],["dc.rights","CC BY 4.0"],["dc.rights.holder","Bauer et al; licensee BioMed Central Ltd."],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","The Integrated Data Repository Toolkit (IDRT): accelerating translational research infrastructures"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","102634"],["dc.bibliographiccitation.journal","Multiple Sclerosis and Related Disorders"],["dc.bibliographiccitation.volume","47"],["dc.contributor.author","Peeters, Liesbet M."],["dc.contributor.author","Parciak, Tina"],["dc.contributor.author","Kalra, Dipak"],["dc.contributor.author","Moreau, Yves"],["dc.contributor.author","Kasilingam, Elisabeth"],["dc.contributor.author","van Galen, Pieter"],["dc.contributor.author","Thalheim, Christoph"],["dc.contributor.author","Uitdehaag, Bernard"],["dc.contributor.author","Vermersch, Patrick"],["dc.contributor.author","Hellings, Niels"],["dc.contributor.author","Stinissen, Piet"],["dc.contributor.author","Van Wijmeersch, Bart"],["dc.contributor.author","Ardeshirdavani, Amin"],["dc.contributor.author","Pirmani, Ashkan"],["dc.contributor.author","De Brouwer, Edward"],["dc.contributor.author","Bauer, Christian Robert"],["dc.contributor.author","Krefting, Dagmar"],["dc.contributor.author","Ribbe, Stephanie"],["dc.contributor.author","Middleton, Rod"],["dc.contributor.author","Stahmann, Alexander"],["dc.contributor.author","Comi, Giancarlo"],["dc.date.accessioned","2021-04-14T08:30:26Z"],["dc.date.available","2021-04-14T08:30:26Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1016/j.msard.2020.102634"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83235"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.issn","2211-0348"],["dc.title","Multiple Sclerosis Data Alliance – A global multi-stakeholder collaboration to scale-up real world data research"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","BMC Bioinformatics"],["dc.bibliographiccitation.volume","21"],["dc.contributor.author","Suhr, M."],["dc.contributor.author","Lehmann, C."],["dc.contributor.author","Bauer, C. R."],["dc.contributor.author","Bender, T."],["dc.contributor.author","Knopp, C."],["dc.contributor.author","Freckmann, L."],["dc.contributor.author","Öst Hansen, B."],["dc.contributor.author","Henke, C."],["dc.contributor.author","Aschenbrandt, G."],["dc.contributor.author","Kühlborn, L. K."],["dc.contributor.author","Rheinländer, S."],["dc.contributor.author","Weber, L."],["dc.contributor.author","Marzec, B."],["dc.contributor.author","Hellkamp, M."],["dc.contributor.author","Wieder, P."],["dc.contributor.author","Sax, U."],["dc.contributor.author","Kusch, H."],["dc.contributor.author","Nussbeck, S. Y."],["dc.date.accessioned","2021-04-14T08:32:27Z"],["dc.date.available","2021-04-14T08:32:27Z"],["dc.date.issued","2020"],["dc.description.sponsorship","Open-Access-Publikationsfonds 2021"],["dc.identifier.doi","10.1186/s12859-020-03928-1"],["dc.identifier.pmid","33334310"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17711"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83924"],["dc.identifier.url","https://sfb1002.med.uni-goettingen.de/production/literature/publications/374"],["dc.identifier.url","https://sfb1190.med.uni-goettingen.de/production/literature/publications/132"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.notes.intern","Merged from goescholar"],["dc.relation","SFB 1002: Modulatorische Einheiten bei Herzinsuffizienz"],["dc.relation","SFB 1002 | INF: Unterstützung der SFB 1002 Forschungsdatenintegration, -visualisierung und -nachnutzung"],["dc.relation","SFB 1190: Transportmaschinen und Kontaktstellen zellulärer Kompartimente"],["dc.relation","SFB 1190 | Z03: Synthetische genetische Analyse, automatisierte Mikroskopie und Bildanalyse"],["dc.relation.eissn","1471-2105"],["dc.relation.orgunit","Gesellschaft für wissenschaftliche Datenverarbeitung"],["dc.relation.workinggroup","RG Nußbeck"],["dc.relation.workinggroup","RG Schwappach (Membrane Protein Biogenesis)"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Menoci: lightweight extensible web portal enhancing data management for biomedical research projects"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]