Direct stochastic optical reconstruction microscopy with standard fluorescent probes

van de Linde S, Löschberger A, Klein T, Heidbreder M, Wolter S, Heilemann M, Sauer M (2011)
Nature Protocols 6(7): 991-1009.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Erscheinungsjahr
2011
Zeitschriftentitel
Nature Protocols
Band
6
Ausgabe
7
Seite(n)
991-1009
ISSN
1754-2189
eISSN
1750-2799
Page URI
https://pub.uni-bielefeld.de/record/2444529

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van de Linde S, Löschberger A, Klein T, et al. Direct stochastic optical reconstruction microscopy with standard fluorescent probes. Nature Protocols. 2011;6(7):991-1009.
van de Linde, S., Löschberger, A., Klein, T., Heidbreder, M., Wolter, S., Heilemann, M., & Sauer, M. (2011). Direct stochastic optical reconstruction microscopy with standard fluorescent probes. Nature Protocols, 6(7), 991-1009. https://doi.org/10.1038/nprot.2011.336
van de Linde, S., Löschberger, A., Klein, T., Heidbreder, M., Wolter, S., Heilemann, M., and Sauer, M. (2011). Direct stochastic optical reconstruction microscopy with standard fluorescent probes. Nature Protocols 6, 991-1009.
van de Linde, S., et al., 2011. Direct stochastic optical reconstruction microscopy with standard fluorescent probes. Nature Protocols, 6(7), p 991-1009.
S. van de Linde, et al., “Direct stochastic optical reconstruction microscopy with standard fluorescent probes”, Nature Protocols, vol. 6, 2011, pp. 991-1009.
van de Linde, S., Löschberger, A., Klein, T., Heidbreder, M., Wolter, S., Heilemann, M., Sauer, M.: Direct stochastic optical reconstruction microscopy with standard fluorescent probes. Nature Protocols. 6, 991-1009 (2011).
van de Linde, Sebastian, Löschberger, A., Klein, T., Heidbreder, Meike, Wolter, Steve, Heilemann, Mike, and Sauer, M. “Direct stochastic optical reconstruction microscopy with standard fluorescent probes”. Nature Protocols 6.7 (2011): 991-1009.

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Advances in three-dimensional super-resolution nanoscopy.
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Methodology for Quantitative Characterization of Fluorophore Photoswitching to Predict Superresolution Microscopy Image Quality.
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PFA fixation enables artifact-free super-resolution imaging of the actin cytoskeleton and associated proteins.
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Super-resolution optical microscopy study of telomere structure.
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Super-Resolution Imaging of Plasma Membrane Proteins with Click Chemistry.
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Automatic Bayesian single molecule identification for localization microscopy.
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Light-induced cell damage in live-cell super-resolution microscopy.
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A MYC-Driven Change in Mitochondrial Dynamics Limits YAP/TAZ Function in Mammary Epithelial Cells and Breast Cancer.
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The chlamydial organism Simkania negevensis forms ER vacuole contact sites and inhibits ER-stress.
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Yamanaka M, Smith NI, Fujita K., Microscopy (Oxf) 63(3), 2014
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Geminate recombination as a photoprotection mechanism for fluorescent dyes.
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High abundance of BDNF within glutamatergic presynapses of cultured hippocampal neurons.
Andreska T, Aufmkolk S, Sauer M, Blum R., Front Cell Neurosci 8(), 2014
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Structural analysis of respiratory syncytial virus reveals the position of M2-1 between the matrix protein and the ribonucleoprotein complex.
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Facile method to stain the bacterial cell surface for super-resolution fluorescence microscopy.
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A spontaneously blinking fluorophore based on intramolecular spirocyclization for live-cell super-resolution imaging.
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Super-resolution imaging of plasma membrane glycans.
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Multivalent ligands control stem cell behaviour in vitro and in vivo.
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