In Vivo Imaging of Membrane-Associated Glycans in Developing Zebrafish
By Scott T. Laughlin, Jeremy M. Baskin, S. Amacher, Carolyn R. Bertozzi. Science, 2008
893 citations recorded by the source corpus.
Subfields: Cell Biology, Immunology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/9a8e1c7c5cd91f3b909332dfcf943f9468919a27
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In Cell Biology
In Immunology
In Molecular Biology
- M. Finn
- Ralph Weissleder
- Craig S Mckay
- S. Hilderbrand
- K. Anseth
- Cole A. DeForest
- B. Polizzotti
- Vasilis Ntziachristos
Citations in the corpus
- Click Chemistry in Complex Mixtures: Bioorthogonal Bioconjugation (2014, background): “They can be easily introduced into biomolecules such as glycans (Baskin et al., 2007; Chang et al., 2010; Laughlin et al., 2008), proteins (Beatty et al.”
- Tetrazine-Based Cycloadditions: Application to Pretargeted Live Cell Imaging (2008, background): “Despite these shortcomings, the cycloaddition reaction between azides and ring-strained cyclooctynes has been employed for imaging of cells (4) and zebra fish embryos (10).”
- Click hydrogels, microgels and nanogels: emerging platforms for drug delivery and tissue engineering. (2014, background): “In the past years, several cyclooctyne molecules were found to react quickly with azides without a copper catalyst as a result of ring strain and electron-withdrawing fluorine substituents [47,48].”
- Surface functionalized exosomes as targeted drug delivery vehicles for cerebral ischemia therapy. (2018, background): “zebrafish, and mice without apparent toxicity or ph ysiological perturbation [55-57].”
- Sequential Click Reactions for Synthesizing and Patterning 3D Cell Microenvironments (2009, methodology): “Specifically, azide-labelled cell-surface glycans were reacted with fluorescently labelled cyclooctynes in vivo to enable the visualization of dynamic subcellular development within zebra-fish embryo”