Mats G L Gustafsson
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Explore the profile of Mats G L Gustafsson including associated specialties, affiliations and a list of published articles.
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11
Citations
2482
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Recent Articles
1.
Abrahamsson S, Chen J, Hajj B, Stallinga S, Katsov A, Wisniewski J, et al.
Nat Methods
. 2012 Dec;
10(1):60-3.
PMID: 23223154
Conventional acquisition of three-dimensional (3D) microscopy data requires sequential z scanning and is often too slow to capture biological events. We report an aberration-corrected multifocus microscopy method capable of producing...
2.
Fiolka R, Shao L, Rego E, Davidson M, Gustafsson M
Proc Natl Acad Sci U S A
. 2012 Mar;
109(14):5311-5.
PMID: 22431626
Previous implementations of structured-illumination microscopy (SIM) were slow or designed for one-color excitation, sacrificing two unique and extremely beneficial aspects of light microscopy: live-cell imaging in multiple colors. This is...
3.
Rego E, Shao L, Macklin J, Winoto L, Johansson G, Kamps-Hughes N, et al.
Proc Natl Acad Sci U S A
. 2011 Dec;
109(3):E135-43.
PMID: 22160683
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 resolution of a...
4.
Shao L, Kner P, Rego E, Gustafsson M
Nat Methods
. 2011 Oct;
8(12):1044-6.
PMID: 22002026
Three-dimensional (3D) structured-illumination microscopy (SIM) can double the lateral and axial resolution of a wide-field fluorescence microscope but has been too slow for live imaging. Here we apply 3D SIM...
5.
Kner P, Chhun B, Griffis E, Winoto L, Gustafsson M
Nat Methods
. 2009 May;
6(5):339-42.
PMID: 19404253
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...
6.
Schermelleh L, Carlton P, Haase S, Shao L, Winoto L, Kner P, et al.
Science
. 2008 Jun;
320(5881):1332-6.
PMID: 18535242
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...
7.
8.
Gustafsson M, Shao L, Carlton P, Wang C, Golubovskaya I, Cande W, et al.
Biophys J
. 2008 Mar;
94(12):4957-70.
PMID: 18326650
Structured illumination microscopy is a method that can increase the spatial resolution of wide-field fluorescence microscopy beyond its classical limit by using spatially structured illumination light. Here we describe how...
9.
Shao L, Isaac B, Uzawa S, Agard D, Sedat J, Gustafsson M
Biophys J
. 2008 Mar;
94(12):4971-83.
PMID: 18326649
A new type of wide-field fluorescence microscopy is described, which produces 100-nm-scale spatial resolution in all three dimensions, by using structured illumination in a microscope that has two opposing objective...
10.
Gustafsson M
Proc Natl Acad Sci U S A
. 2005 Sep;
102(37):13081-6.
PMID: 16141335
Contrary to the well known diffraction limit, the fluorescence microscope is in principle capable of unlimited resolution. The necessary elements are spatially structured illumination light and a nonlinear dependence of...