Richter, Katharina N.

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Scientific Reports"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Richter, Katharina N."],["dc.contributor.author","Patzelt, Christina"],["dc.contributor.author","Phan, Nhu T. N."],["dc.contributor.author","Rizzoli, Silvio O."],["dc.date.accessioned","2020-12-10T18:11:03Z"],["dc.date.available","2020-12-10T18:11:03Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1038/s41598-019-45729-4"],["dc.identifier.pmid","31239503"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16340"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/73893"],["dc.identifier.url","https://sfb1190.med.uni-goettingen.de/production/literature/publications/75"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.relation","SFB 1190: Transportmaschinen und Kontaktstellen zellulärer Kompartimente"],["dc.relation","SFB 1190 | P09: Proteinsortierung in der Synapse: Prinzipien und molekulare Organisation"],["dc.relation.workinggroup","RG Rizzoli (Quantitative Synaptology in Space and Time)"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Antibody-driven capture of synaptic vesicle proteins on the plasma membrane enables the analysis of their interactions with other synaptic proteins"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","189"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Polymer Degradation and Stability"],["dc.bibliographiccitation.lastpage","199"],["dc.bibliographiccitation.volume","89"],["dc.contributor.author","Xie, Y."],["dc.contributor.author","Krause, A."],["dc.contributor.author","Mai, Carsten"],["dc.contributor.author","Militz, Holger"],["dc.contributor.author","Richter, K."],["dc.contributor.author","Urban, K."],["dc.contributor.author","Evans, P. D."],["dc.date.accessioned","2018-11-07T11:20:26Z"],["dc.date.available","2018-11-07T11:20:26Z"],["dc.date.issued","2005"],["dc.description.abstract","N-methylol compounds are used as a wrinkle-resistant finish in the textile industry. They are expected to enhance the resistance of wood to weathering because they can cross-link the cell wall and dimensionally stabilise wood. Scots pine veneers were modified with 1,3-dimethylol-4,5-dihydroxyethyleneurea (DMDHEU) to weight percent gains (WPG) of 10 %, 27 % or 48 % and exposed to artificial weathering. Initially, weight losses of unmodified veneers were significantly greater than those of DMDHEU treated specimens even though DMDHEU was leached from wood at a higher rate than loss of wood substance. The weight losses of all treated veneers after 144 h of weathering, however, were similar to those of the unmodified controls. Therefore we conclude that in the short term DMDHEU treatment can restrict weight losses of wood during weathering, which occur due to degradation of lignin and hemicellulose and loss of degraded wood fragments from wood. Infrared spectroscopy suggested that treatment of wood veneers with DMDHEU to high WPG (48 %) stabilised lignin to some extent. Tensile strength losses of DMDHEU treated veneers during weathering were lower than those of untreated veneers. DMDHEU treatment, however, had a deleterious effect on the tensile strength of the veneers, possibly associated with the presence of magnesium chloride catalyst in the treatment solution. Scanning electron microscopy revealed that DMDHEU treatment was highly effective at preventing the degradation of the wood cell wall during weathering. Tracheids in unmodified veneers became distorted within 48 It of weathering exposure, whereas cells in modified veneers, especially those reacted to higher weight percent gains, retained their shape even after 144 h weathering. (c) 2004 Elsevier Ltd. All rights reserved."],["dc.identifier.doi","10.1016/j.polymdegradstab.2004.08.017"],["dc.identifier.isi","000230156900001"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/55536"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Sci Ltd"],["dc.relation.issn","0141-3910"],["dc.title","Weathering of wood modified with the N-methylol compound 1,3-dimethylol-4,5-dihydroxyethyleneurea"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Scientific Reports"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Richter, Katharina N."],["dc.contributor.author","Wildhagen, Hanna"],["dc.contributor.author","Helm, Martin S."],["dc.contributor.author","Ußling, Jan-Eike"],["dc.contributor.author","Schikorski, Thomas"],["dc.contributor.author","Rizzoli, Silvio O."],["dc.date.accessioned","2020-12-10T18:10:12Z"],["dc.date.available","2020-12-10T18:10:12Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1038/s41598-018-33130-6"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/15451"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/73888"],["dc.identifier.url","https://sfb1190.med.uni-goettingen.de/production/literature/publications/55"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.relation","SFB 1190: Transportmaschinen und Kontaktstellen zellulärer Kompartimente"],["dc.relation","SFB 1190 | P09: Proteinsortierung in der Synapse: Prinzipien und molekulare Organisation"],["dc.relation.workinggroup","RG Rizzoli (Quantitative Synaptology in Space and Time)"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Comparative synaptosome imaging: a semi-quantitative method to obtain copy numbers for synaptic and neuronal proteins"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","139"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","The EMBO journal"],["dc.bibliographiccitation.lastpage","159"],["dc.bibliographiccitation.volume","37"],["dc.contributor.author","Richter, Katharina N."],["dc.contributor.author","Revelo, Natalia H."],["dc.contributor.author","Seitz, Katharina J."],["dc.contributor.author","Helm, Martin S."],["dc.contributor.author","Sarkar, Deblina"],["dc.contributor.author","Saleeb, Rebecca S."],["dc.contributor.author","d'Este, Elisa"],["dc.contributor.author","Eberle, Jessica"],["dc.contributor.author","Wagner, Eva"],["dc.contributor.author","Vogl, Christian"],["dc.contributor.author","Lazaro, Diana F."],["dc.contributor.author","Richter, Frank"],["dc.contributor.author","Coy-Vergara, Javier"],["dc.contributor.author","Coceano, Giovanna"],["dc.contributor.author","Boyden, Edward S."],["dc.contributor.author","Duncan, Rory R."],["dc.contributor.author","Hell, Stefan W."],["dc.contributor.author","Lauterbach, Marcel A."],["dc.contributor.author","Lehnart, Stephan E."],["dc.contributor.author","Moser, Tobias"],["dc.contributor.author","Outeiro, Tiago F."],["dc.contributor.author","Rehling, Peter"],["dc.contributor.author","Schwappach, Blanche"],["dc.contributor.author","Testa, Ilaria"],["dc.contributor.author","Zapiec, Bolek"],["dc.contributor.author","Rizzoli, Silvio O."],["dc.date.accessioned","2018-01-09T14:09:53Z"],["dc.date.available","2018-01-09T14:09:53Z"],["dc.date.issued","2018"],["dc.description.abstract","Paraformaldehyde (PFA) is the most commonly used fixative for immunostaining of cells, but has been associated with various problems, ranging from loss of antigenicity to changes in morphology during fixation. We show here that the small dialdehyde glyoxal can successfully replace PFA Despite being less toxic than PFA, and, as most aldehydes, likely usable as a fixative, glyoxal has not yet been systematically tried in modern fluorescence microscopy. Here, we tested and optimized glyoxal fixation and surprisingly found it to be more efficient than PFA-based protocols. Glyoxal acted faster than PFA, cross-linked proteins more effectively, and improved the preservation of cellular morphology. We validated glyoxal fixation in multiple laboratories against different PFA-based protocols and confirmed that it enabled better immunostainings for a majority of the targets. Our data therefore support that glyoxal can be a valuable alternative to PFA for immunostaining."],["dc.identifier.doi","10.15252/embj.201695709"],["dc.identifier.pmid","29146773"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/15063"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/11599"],["dc.identifier.url","https://sfb1002.med.uni-goettingen.de/production/literature/publications/195"],["dc.identifier.url","https://sfb1190.med.uni-goettingen.de/production/literature/publications/15"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.relation","SFB 1002: Modulatorische Einheiten bei Herzinsuffizienz"],["dc.relation","SFB 1002 | A09: Lokale molekulare Nanodomänen-Regulation der kardialen Ryanodin-Rezeptor-Funktion"],["dc.relation","SFB 1190: Transportmaschinen und Kontaktstellen zellulärer Kompartimente"],["dc.relation","SFB 1190 | P09: Proteinsortierung in der Synapse: Prinzipien und molekulare Organisation"],["dc.relation.eissn","1460-2075"],["dc.relation.workinggroup","RG Hell"],["dc.relation.workinggroup","RG Lehnart (Cellular Biophysics and Translational Cardiology Section)"],["dc.relation.workinggroup","RG Rehling (Mitochondrial Protein Biogenesis)"],["dc.relation.workinggroup","RG Schwappach (Membrane Protein Biogenesis)"],["dc.relation.workinggroup","RG Rizzoli (Quantitative Synaptology in Space and Time)"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Glyoxal as an alternative fixative to formaldehyde in immunostaining and super-resolution microscopy"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3975"],["dc.bibliographiccitation.issue","23"],["dc.bibliographiccitation.journal","Materials"],["dc.bibliographiccitation.volume","12"],["dc.contributor.author","Böker, Kai O."],["dc.contributor.author","Richter, Katharina"],["dc.contributor.author","Jäckle, Katharina"],["dc.contributor.author","Taheri, Shahed"],["dc.contributor.author","Grunwald, Ingo"],["dc.contributor.author","Borcherding, Kai"],["dc.contributor.author","von Byern, Janek"],["dc.contributor.author","Hartwig, Andreas"],["dc.contributor.author","Wildemann, Britt"],["dc.contributor.author","Schilling, Arndt F."],["dc.contributor.author","Lehmann, Wolfgang"],["dc.date.accessioned","2020-12-10T18:47:15Z"],["dc.date.available","2020-12-10T18:47:15Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.3390/ma12233975"],["dc.identifier.eissn","1996-1944"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16940"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/78693"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.publisher","MDPI"],["dc.relation.eissn","1996-1944"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Current State of Bone Adhesives—Necessities and Hurdles"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","020901"],["dc.bibliographiccitation.firstpage","020901"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Neurophotonics"],["dc.bibliographiccitation.volume","4"],["dc.contributor.author","Richter, Katharina N."],["dc.contributor.author","Rizzoli, Silvio O."],["dc.contributor.author","Jähne, Sebastian"],["dc.contributor.author","Vogts, Angela"],["dc.contributor.author","Lovric, Jelena"],["dc.date.accessioned","2020-12-10T18:36:36Z"],["dc.date.available","2020-12-10T18:36:36Z"],["dc.date.issued","2017"],["dc.description.abstract","Investigating the detailed substructure of the cell is beyond the ability of conventional optical microscopy. Electron microscopy, therefore, has been the only option for such studies for several decades. The recent implementation of several super-resolution optical microscopy techniques has rendered the investigation of cellular substructure easier and more efficient. Nevertheless, optical microscopy only provides an image of the present structure of the cell, without any information on its long-temporal changes. These can be investigated by combining super-resolution optics with a nonoptical imaging technique, nanoscale secondary ion mass spectrometry, which investigates the isotopic composition of the samples. The resulting technique, combined isotopic and optical nanoscopy, enables the investigation of both the structure and the \"history\" of the cellular elements. The age and the turnover of cellular organelles can be read by isotopic imaging, while the structure can be analyzed by optical (fluorescence) approaches. We present these technologies, and we discuss their implementation for the study of biological samples. We conclude that, albeit complex, this type of technology is reliable enough for mass application to cell biology."],["dc.identifier.doi","10.1117/1.NPh.4.2.020901"],["dc.identifier.issn","2329-423X"],["dc.identifier.pmid","28466025"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/14911"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76685"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.rights","CC BY-NC-SA 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by-nc-sa/3.0"],["dc.title","Review of combined isotopic and optical nanoscopy"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]