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cells beyond the diffraction limit with structured illumination microscopy and Bayesian image reconstruction"" data-category="" data-cropid="" data-dimen="" data-id="EC4A3E43-967E-4092-BAFC-3E40BBF6159A"> Supporting data for "Imaging tissues and cells beyond the diffraction limit with structured illumination microscopy and Bayesian image reconstruction"
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- 关键词：
- Imaging structured illumination microscopy simtoolbox fluorescence sim super-resolution microscopy bayesian methods live cell imaging
- DOI：
- doi:10.5524/100514
- 摘要：
- Structured illumination microscopy (SIM) is a family of methods in optical fluorescence microscopy that can achieve both optical sectioning and super
Data from: A tunable refractive index matching medium for live imaging cells, tissues and model organisms
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- 关键词：
- DOI：
- doi:10.5061/dryad.83gp7
- 摘要：
- In light microscopy, refractive index mismatches between media and sample cause spherical aberrations that often limit penetration depth and r
Data from: A transgenic quail model that enables dynamic imaging of amniote embryogenesis
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- DOI：
- doi:10.5061/dryad.74bk6
- 摘要：
- ments. Dynamic imaging, combined with quantitative analysis, is ideal for investigating fundamental questions in developmental biology involving cell
Data from: Spatially coordinated dynamic gene transcription in living pituitary tissue
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- 关键词：
- live-cell microscopy;Pituitary;Transcription Dynamics;Spatial Organisation;stochastic modelling
- DOI：
- doi:10.5061/dryad.s04bb
- 摘要：
- lactin gene expression. Our findings identify how heterogeneous transcriptional dynamics of single cells may contribute to overall tissue behaviour.
Data from: Conformational dynamics in TRPV1 channels reported by an encoded coumarin amino acid
- 负责人：
- DOI：
- doi:10.5061/dryad.1kc2c
- 摘要：
- ally encoded at Y671, a residue proximal to the selectivity filter. Total internal reflection fluorescence microscopy was performed to image
Data from: Rev7 and 53BP1/Crb2 prevent RecQ helicase-dependent hyper-resection of DNA double-strand breaks
- 负责人：
- 关键词：
- live-cell microscopy;end resection;Schizosaccharomyces pombe;DNA repair;DNA double-strand break
- DOI：
- doi:10.5061/dryad.1db5500
- 摘要：
- : the exonuclease Exo1, or the combination of a RecQ helicase and Dna2. Here, we develop a single cell microscopy assay that allows the distinct phases
Data from: How do algae form multicellular groups?
- 负责人：
- DOI：
- doi:10.5061/dryad.vb665
- 摘要：
- Daphnia magna. Results: Fluorescence microscopy and time-lapse photography revealed that, in response to predator supernatant/live predators, these algae form gro
Data from: Single-molecule imaging correlates decreasing nuclear volume with increasing TF-chromatin associations during zebrafish development
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- 关键词：
- DOI：
- doi:10.5061/dryad.g154580
- 摘要：
- gely unknown. We establish single molecule tracking in live developing zebrafish embryos using reflected light-sheet microscopy to visualize two fluoresce
Data from: The AAA protein Msp1 mediates clearance of excess tail-anchored proteins from the peroxisomal membrane
- 负责人：
- 关键词：
- DOI：
- doi:10.5061/dryad.pc4d6
- 摘要：
- xisomes evade Msp1 surveillance. We used live-cell quantitative cell microscopy tools and drug-inducible gene expression to dissect Msp1 function. We found tha
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