Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Adrien Descloux"'
Autor:
Vytautas Navikas, Samuel M. Leitao, Kristin S. Grussmayer, Adrien Descloux, Barney Drake, Klaus Yserentant, Philipp Werther, Dirk-Peter Herten, Richard Wombacher, Aleksandra Radenovic, Georg E. Fantner
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
Methods for imaging the 3D cell surface often require physical interaction. Here the authors report the combination of scanning ion conductance microscopy (SICM) and live-cell super-resolution optical fluctuation imaging (SOFI) for the non-invasive t
Externí odkaz:
https://doaj.org/article/8564f2433b224019a49df1f8e9b184c1
Autor:
Dora Mahecic, Adrien Descloux, Suliana Manley, Aleksandra Radenovic, Kristin S. Grußmayer, Vytautas Navikas
Publikováno v:
ACS Photonics. 8:2440-2449
All fluorescence super-resolution microscopy techniques present trade-offs between, for example, resolution, acquisition speed, and live-cell compatibility. Structured illumination microscopy (SIM) improves the resolution through successive imaging o
Autor:
Kristin S. Grußmayer, Marcel Leutenegger, Stefan Geissbuehler, Adrien Descloux, Theo Lasser, Aleksandra Radenovic, Tomas Lukes
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-8 (2020)
Nature Communications
Nature Communications
Super-resolution optical fluctuation imaging (SOFI) provides a resolution beyond the diffraction limit by analysing stochastic fluorescence fluctuations with higher-order statistics. Using nth order spatio-temporal cross-cumulants the spatial resolut
Autor:
Adrien Descloux, Samuel M. Leitao, Georg E. Fantner, Richard Wombacher, Barney Drake, Klaus Yserentant, Dirk-Peter Herten, Philipp Werther, Aleksandra Radenovic, Kristin S. Grussmayer, Vytautas Navikas
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
High-resolution live-cell imaging is necessary to study complex biological phenomena. Modern fluorescence microscopy methods are increasingly combined with complementary, label-free techniques to put the fluorescence information into the cellular con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8bd65f8b8bd0d9f308465de197e6714
https://pubmed.ncbi.nlm.nih.gov/34315910/
https://pubmed.ncbi.nlm.nih.gov/34315910/
Publikováno v:
Nature Methods. 17:1061-1063
Autor:
Mathieu Di Franco, Jérôme Extermann, Alessio Mylonas, Yoan Neuenschwander, Enrico Pomarico, Aleksandra Radenovic, David Nguyen, Adrien Descloux, Arielle Planchette, Cédric Schmidt, Gabriel Giardina
Publikováno v:
Biomed Opt Express
Optical projection tomography (OPT) is a powerful tool for three-dimensional imaging of mesoscopic biological samples with great use for biomedical phenotyping studies. We present a fluorescent OPT platform that enables direct visualization of biolog
Autor:
Adrien Descloux, Aleksandra Radenovic, Vytautas Navikas, Kristin S. Grussmayer, Sanjin Marion
Publikováno v:
Nanophotonics, 10(9)
Nanophotonics, Vol 10, Iss 9, Pp 2451-2458 (2021)
Nanophotonics, Vol 10, Iss 9, Pp 2451-2458 (2021)
A variety of modern super-resolution microscopy methods provide researchers with previously inconceivable biological sample imaging opportunities at a molecular resolution. All of these techniques excel at imaging samples that are close to the covers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::584e95646605568b36708e603b2b9017
http://resolver.tudelft.nl/uuid:791e4b7b-7a00-47cf-93b8-02e103f6ac9b
http://resolver.tudelft.nl/uuid:791e4b7b-7a00-47cf-93b8-02e103f6ac9b
Autor:
Kristin S. Grussmayer, Dirk-Peter Herten, Barney Drake, Richard Wombacher, Klaus Yserentant, Georg E. Fantner, Samuel M. Leitao, Vytautas Navikas, Adrien Descloux, Philipp Werther, Aleksandra Radenovic
High-resolution live-cell imaging is necessary to study complex biological phenomena. Modern fluorescence microscopy methods are increasingly combined with complementary, label-free techniques to put the fluorescence information into the cellular con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::258ca8bab790d8388631b720dcff3a4b
https://doi.org/10.1101/2020.11.09.374157
https://doi.org/10.1101/2020.11.09.374157
Publikováno v:
Communications Biology
Communications Biology, Vol 4, Iss 1, Pp 1-6 (2021)
Communications Biology, Vol 4, Iss 1, Pp 1-6 (2021)
Localization microscopy is a super-resolution imaging technique that relies on the spatial and temporal separation of blinking fluorescent emitters. These blinking events can be individually localized with a precision significantly smaller than the c
Autor:
Peter Dedecker, Vytautas Navikas, Thomas R Huser, Wolfgang Hübner, Andreas Markwirth, Aleksandra Radenovic, Robin Van den Eynde, Marcel Müller, Adrien Descloux, Theo Lasser, Tomas Lukes
Super-resolution structured illumination microscopy (SR-SIM) can be conducted at video-rate acquisition speeds when combined with high-speed spatial light modulators and sCMOS cameras, rendering it particularly suitable for live cell imaging. If, how
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b60721482231b052be143b08d2104c