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Biophysical Journal|February 1, 1990
Determination of three-dimensional imaging properties of a light microscope system. Partial confocal behavior in epifluorescence microscopyY Hiraoka, J W Sedat, D A AgardCell|April 9, 1993
Multiple chromosomal populations of topoisomerase II detected in vivo by time-lapse, three-dimensional wide-field microscopyJ R Swedlow, J W Sedat, D A AgardJournal of Microscopy|August 12, 1999
I5M: 3D widefield light microscopy with better than 100 nm axial resolutionM G Gustafsson, D A Agard, J W SedatNature|October 31, 1998
Unfolded conformations of alpha-lytic protease are more stable than its native stateJ L Sohl, S S Jaswal, D A AgardSeminars in Cell Biology|August 1, 1992
An extended view of nuclear lamin structure, function, and dynamicsM R Paddy, D A Agard, J W SedatJournal of Structural Biology|January 27, 1998
Practical image restoration of thick biological specimens using multiple focus levels in transmission electron microscopyK F Han, J W Sedat, D A AgardMethods in Enzymology|October 5, 2010
Automated data collection for electron microscopic tomographyShawn Q Zheng, J W Sedat, D A AgardJournal of Molecular Biology|August 4, 1995
Functional linkage between the active site of alpha-lytic protease and distant regions of structure: scanning alanine mutagenesis of a surface loop affects activity and substrate specificityJ E Mace, B J Wilk, D A AgardCurrent Opinion in Cell Biology|June 1, 1993
Chromosome structure inside the nucleusJ R Swedlow, D A Agard, J W SedatProteins|January 1, 1991
Free energy calculations on binding and catalysis by alpha-lytic protease: the role of substrate size in the P1 pocketJ W Caldwell, D A Agard, P A KollmanPageof 187