- Alternative title
-
Hochaufgelöste Mikroskopie von Sphingolipiden und Protein Nanodomänen
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Würzburg, Universität Würzburg, Dissertation, 2020
- Keyword
-
Microscopy
Sphingolipids
Sphingolipide
Lipide
Einzelmolekülmikroskopie
Click-Chemie
Lipid Raft
- Event
-
Veröffentlichung
- (where)
-
Würzburg
- (who)
-
Universität Würzburg
- (when)
-
2021
- Creator
-
Schlegel, Jan
- Contributor
-
Sauer, Markus
Terpitz, Ulrich
Wegener, Christian
Heinze, Katrin
- DOI
-
10.25972/OPUS-22959
- URN
-
urn:nbn:de:bvb:20-opus-229596
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:44 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Schlegel, Jan
- Sauer, Markus
- Terpitz, Ulrich
- Wegener, Christian
- Heinze, Katrin
- Universität Würzburg
Time of origin
- 2021
Other Objects (12)
Expansion Microscopy combined with Super-Resolution Fluorescence Microscopy
Super-Resolution Microscopy of Synaptic Proteins
Super-resolution microscopy of plasma membrane receptors
Bioorthogonal labeling of neuronal proteins using super-resolution fluorescence microscopy
Super-resolution microscopy of the synaptic active zone
Quantitative Analysis of Membrane Components using Super-Resolution Microscopy
Single-molecule localization algorithms in super-resolution microscopy
Super-resolution microscopy of plasma membrane receptors and intracellular pathogens
Light-induced cell damage in live-cell super-resolution microscopy
Improving Super-Resolution Microscopy Data Reconstruction and Evaluation by Developing Advanced Processing Algorithms and Artifcial Neuronal Networks
Sharpening super-resolution by single molecule localization microscopy in front of a tuned mirror
Correlative live and fixed cell superresolution microscopy
Expansion Microscopy combined with Super-Resolution Fluorescence Microscopy
Super-Resolution Microscopy of Synaptic Proteins
Super-resolution microscopy of plasma membrane receptors
Bioorthogonal labeling of neuronal proteins using super-resolution fluorescence microscopy
Super-resolution microscopy of the synaptic active zone
Quantitative Analysis of Membrane Components using Super-Resolution Microscopy
Single-molecule localization algorithms in super-resolution microscopy
Super-resolution microscopy of plasma membrane receptors and intracellular pathogens
Light-induced cell damage in live-cell super-resolution microscopy
Improving Super-Resolution Microscopy Data Reconstruction and Evaluation by Developing Advanced Processing Algorithms and Artifcial Neuronal Networks
Sharpening super-resolution by single molecule localization microscopy in front of a tuned mirror
Correlative live and fixed cell superresolution microscopy
Expansion Microscopy combined with Super-Resolution Fluorescence Microscopy
Super-Resolution Microscopy of Synaptic Proteins
Super-resolution microscopy of plasma membrane receptors
Bioorthogonal labeling of neuronal proteins using super-resolution fluorescence microscopy
Super-resolution microscopy of the synaptic active zone
Quantitative Analysis of Membrane Components using Super-Resolution Microscopy
Single-molecule localization algorithms in super-resolution microscopy
Super-resolution microscopy of plasma membrane receptors and intracellular pathogens
Light-induced cell damage in live-cell super-resolution microscopy
Improving Super-Resolution Microscopy Data Reconstruction and Evaluation by Developing Advanced Processing Algorithms and Artifcial Neuronal Networks
Sharpening super-resolution by single molecule localization microscopy in front of a tuned mirror