Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Lukman Winoto"'
Publikováno v:
In Optics Communications 2000 180(1):73-79
Autor:
M. Cristina Cardoso, Brian Burke, Heinrich Leonhardt, Sebastian Haase, Lin Shao, Peter M. Carlton, Mats G. L. Gustafsson, John W. Sedat, David A. Agard, Peter Kner, Lukman Winoto, Lothar Schermelleh
Fluorescence light microscopy allows multicolor visualization of cellular components with high specificity, but its utility has until recently been constrained by the intrinsic limit of spatial resolution. We applied three-dimensional structured illu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0230c2d927de00f3764e93150dcdf9ed
https://ora.ox.ac.uk/objects/uuid:77841673-47eb-45d4-9ba9-b95c87e00db7
https://ora.ox.ac.uk/objects/uuid:77841673-47eb-45d4-9ba9-b95c87e00db7
Publikováno v:
Journal of Microscopy
In an interferometer-based fluorescence microscope, a beam splitter is often used to combine two emission wavefronts interferometrically. There are two perpendicular paths along which the interference fringes can propagate and normally only one is us
Publikováno v:
Nature methods
Structured-illumination microscopy can double the resolution of the widefield fluorescence microscope but has previously been too slow for dynamic live imaging. Here we demonstrate a high-speed structured-illumination microscope that is capable of 10
Publikováno v:
Optics Communications. 180:73-79
We describe a way to compress Cs atoms in a MOT to temporarily reach spatial densities of 10 12 atoms/cm 3 . The method entails starting off with more atoms than will ultimately be used, and then changing parameters so the atoms rush toward the trap
Publikováno v:
Physical Review A. 59:R19-R22
We report a way to overcome heating due to the reabsorption of scattered light when relatively many atoms are laser cooled at high density. A sample of 8310 Cs atoms, with 6310 atoms cm, is loaded into a deep far-detuned one-dimensional optical latti
Autor:
Nick Kamps-Hughes, Michael W. Davidson, Mats G. L. Gustafsson, Lukman Winoto, E. H. Rego, J. J. Macklin, G. A. Johansson, Lin Shao
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 109(3)
Using ultralow light intensities that are well suited for investigating biological samples, we demonstrate whole-cell superresolution imaging by nonlinear structured-illumination microscopy. Structured-illumination microscopy can increase the spatial
Autor:
Sebastian Haase, James E. Haber, Atsushi Matsuda, Jean-Baptiste Sibarita, Susannah Gordon-Messer, Satoru Uzawa, Mats G. L. Gustafsson, Charles Kervrann, Peter M. Carlton, Jérôme Boulanger, Lukman Winoto, Debra A. Bressan, Peter Kner, Zvi Kam, Lin Shao, John W. Sedat, Jean Salamero, David A. Agard
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2010, 107 (37), pp.16016-16022. ⟨10.1073/pnas.1004037107⟩
Proceedings of the National Academy of Sciences of the United States of America, 2010, 107 (37), pp.16016-16022. ⟨10.1073/pnas.1004037107⟩
Proceedings of the National Academy of Sciences of the United States of America 37 (107), 16016-16022. (2010)
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2010, 107 (37), pp.16016-16022. ⟨10.1073/pnas.1004037107⟩
Proceedings of the National Academy of Sciences of the United States of America, 2010, 107 (37), pp.16016-16022. ⟨10.1073/pnas.1004037107⟩
Proceedings of the National Academy of Sciences of the United States of America 37 (107), 16016-16022. (2010)
International audience; Live fluorescence microscopy has the unique capability to probe dynamic processes, linking molecular components and their localization with function. A key goal of microscopy is to increase spatial and temporal resolution whil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c975ba906a3a818b2634d0773e6a03fa
https://hal.inria.fr/inria-00540978/document
https://hal.inria.fr/inria-00540978/document
Publikováno v:
Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XVI.
Linear Structured Illumination is a powerful technique for increasing the resolution of a fluorescence microscope by a factor of two beyond the diffraction limit. Previously this technique has only been used to image fixed samples because the impleme
Publikováno v:
Microscopy and Microanalysis. 17:20-21
Extended abstract of a paper presented at Microscopy and Microanalysis 2011 in Nashville, Tennessee, USA, August 7–August 11, 2011.