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@ARTICLE{Sahl:130903,
author = {S. J. Sahl and S. Hell$^*$ and S. Jakobs},
title = {{F}luorescence nanoscopy in cell biology.},
journal = {Nature reviews / Molecular cell biology},
volume = {18},
number = {11},
issn = {1471-0080},
address = {London},
publisher = {Macmillan},
reportid = {DKFZ-2017-05979},
pages = {685 - 701},
year = {2017},
abstract = {Fluorescence nanoscopy uniquely combines minimally invasive
optical access to the internal nanoscale structure and
dynamics of cells and tissues with molecular detection
specificity. While the basic physical principles of
super-resolution imaging were discovered in the 1990s, with
initial experimental demonstrations following in 2000, the
broad application of super-resolution imaging to address
cell-biological questions has only more recently emerged.
Nanoscopy approaches have begun to facilitate discoveries in
cell biology and to add new knowledge. One current direction
for method improvement is the ambition to quantitatively
account for each molecule under investigation and assess
true molecular colocalization patterns via multi-colour
analyses. In pursuing this goal, the labelling of individual
molecules to enable their visualization has emerged as a
central challenge. Extending nanoscale imaging into (sliced)
tissue and whole-animal contexts is a further goal. In this
Review we describe the successes to date and discuss current
obstacles and possibilities for further development.},
subtyp = {Review Article},
cin = {E190},
ddc = {570},
cid = {I:(DE-He78)E190-20160331},
pnm = {315 - Imaging and radiooncology (POF3-315)},
pid = {G:(DE-HGF)POF3-315},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:28875992},
doi = {10.1038/nrm.2017.71},
url = {https://inrepo02.dkfz.de/record/130903},
}