000199710 001__ 199710
000199710 005__ 20190130101300.0
000199710 0247_ $$2doi$$a10.1038/nmeth.2972
000199710 022__ $$a1548-7105
000199710 02470 $$2ISI$$a000338321400015
000199710 037__ $$aARTICLE
000199710 245__ $$aFluorogenic probes for live-cell imaging of the cytoskeleton
000199710 260__ $$aLondon$$bNature Publishing Group$$c2014
000199710 269__ $$a2014
000199710 300__ $$a7
000199710 336__ $$aJournal Articles
000199710 520__ $$aWe introduce far-red, fluorogenic probes that combine minimal cytotoxicity with excellent brightness and photostability for fluorescence imaging of actin and tubulin in living cells. Applied in stimulated emission depletion (STED) microscopy, they reveal the ninefold symmetry of the centrosome and the spatial organization of actin in the axon of cultured rat neurons with a resolution unprecedented for imaging cytoskeletal structures in living cells.
000199710 700__ $$aLukinavičius, Gražvydas
000199710 700__ $$0240935$$aReymond, Luc$$g155775
000199710 700__ $$aD'Este, Elisa
000199710 700__ $$0244188$$aMasharina, Anastasiya$$g188795
000199710 700__ $$aGöttfert, Fabian
000199710 700__ $$aTa, Haisen
000199710 700__ $$aGüther, Angelika
000199710 700__ $$aFournier, Mathias
000199710 700__ $$aRizzo, Stefano
000199710 700__ $$aWaldmann, Herbert
000199710 700__ $$aBlaukopf, Claudia
000199710 700__ $$aSommer, Christoph
000199710 700__ $$aGerlich, Daniel W.
000199710 700__ $$aArndt, Hans-Dieter
000199710 700__ $$aHell, Stefan W.
000199710 700__ $$0240057$$aJohnsson, Kai$$g123155
000199710 773__ $$j11$$q731–733$$tNature Methods
000199710 909C0 $$0252027$$pLIP$$xU10102
000199710 909CO $$ooai:infoscience.tind.io:199710$$pSB$$particle
000199710 917Z8 $$x123155
000199710 937__ $$aEPFL-ARTICLE-199710
000199710 973__ $$aEPFL$$rNON-REVIEWED$$sPUBLISHED
000199710 980__ $$aARTICLE